Braixen - pokemon wiki, braxan

Braixen

Biology

Physiology

Braxien is a bipedal fox-like Pokemon; unlike its pre-evolution Fennekin. it now stands upright on two legs. Braxien is covered mainly in bright yellow fur (with a black underside) that resembles a skirt; it has a collar of fluffy white fur below its thin neck and covering on its chest. It has a long pointed snout with a round orange nose, and bright orange eyes. Braxien has tufts of bright orange fur sprouting from its ears. It has a branch embedded in its bushy yellow orange-tipped tail, which it uses as a wand to emit blasts of flame. When pulling its branch from its tail the friction causes the tip of the branch to catch fire.

Behavior

Once Fennekin evolves into Braixen, it no longer eats branches for snacks, but will still keep a tree branch in its tail in order to fight with. Braixen will occasionally wield the branch in battle and use friction to light it on fire, as if it is a wand.

Evolution

Braxien evolves from Fennekin at level 16. It evolves into Delphox at level 36.

Game info

Game locations

Debrox solution indications, side effects, warnings, debax

Debrox solution

Softening, loosening, and removing excessive earwax.

Debrox solution is a form of peroxide. It works by softening and removing earwax.

Do NOT use Debrox solution if:

you are allergic to any ingredient in Debrox solution

you have ear drainage or discharge, ear pain, irritation, rash in the ear, ear injury, hole in the eardrum, broken eardrum, or recent ear surgery

you are dizzy

Contact your doctor or health care provider right away if any of these apply to you.

Before using Debrox solution:

Some medical conditions may interact with Debrox solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Debrox solution. Because little, if any, of Debrox solution is absorbed into the blood, the risk of it interacting with another medicine is low.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Debrox solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Debrox solution:

Use Debrox solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Debrox solution is for use in the ear only. Avoid contact with other mucous membranes and eyes.

To use ear drops, lie down or tilt your head so that the affected ear faces up. For adults, gently pull the earlobe up and back to straighten the ear canal. For children, gently pull the earlobe down and back to straighten the ear canal. Drop the medicine into the ear canal. Keep the ear facing up for several minutes so the medicine can run to the bottom of the ear canal. A clean cotton plug may be gently inserted into the ear canal to prevent medicine from leaking out. To prevent germs from contaminating the medicine, do not touch the applicator to any surface, including the ear. Keep the container tightly closed.

Any wax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe.

Use twice daily for 4 days if necessary, or as directed by your doctor. Do not use Debrox solution for more than 4 days without talking to your doctor.

If you miss a dose of Debrox solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Debrox solution.

Important safety information:

If excessive earwax remains after use of Debrox solution, contact your doctor.

Debrox solution is not recommended for use in CHILDREN younger than 12 years of age except under the advice of a doctor.

PREGNANCY and BREAST-FEEDING: It is unknown if Debrox solution can cause harm to the fetus. If you become pregnant while taking Debrox solution, discuss with your doctor the benefits and risks of using Debrox solution during pregnancy. It is unknown if Debrox solution is excreted in breast milk. If you are or will be breast-feeding while you are using Debrox solution, check with your doctor or pharmacist to discuss the risks to your baby.

Possible side effects of Debrox solution:

All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with this product. Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately.

Proper storage of Debrox solution:

Store Debrox solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Debrox solution out of the reach of children and away from pets.

General information:

If you have any questions about Debrox solution, please talk with your doctor, pharmacist, or other health care provider.

Debrox solution is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take Debrox solution or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about Debrox solution. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to Debrox solution. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using Debrox solution.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about Debrox (carbamide peroxide otic)

Diclofenac - woman s health, koptin

Diclofenac is used to treat pain or inflammation caused by arthritis or ankylosing spondylitis. Diclofenac may also be used for purposes other than those listed in this medication guide.

Use Diclofenac as directed by your doctor.

Take Diclofenac by mouth with or without food. Ask your health care provider any questions you may have about how to use Diclofenac.

Drug Class and Mechanism

Diclofenac is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Diclofenac works by reducing hormones that cause inflammation and pain in the body.

If you miss a dose of Diclofenac, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Store Diclofenac at room temperature between 68 and 77 degrees F (20 and 25 degrees C) in a tightly closed container. Brief periods at temperatures of 59 to 86 degrees F (15 to 30 degrees C) are permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diclofenac out of the reach of children and away from pets.

Do not use Diclofenac if:

you are allergic to any ingredient in Diclofenac; you have had a severe allergic reaction (e. g. severe rash, hives, breathing difficulties, dizziness) to another NSAID (e. g. ibuprofen, naproxen, celecoxib) or aspirin. Contact your doctor or health care provider right away if any of these apply to you.

Important : Diclofenac may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Diclofenac with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Before you start any new medicine, check the label to see if it has diclofenac or another nonsteroidal anti-inflammatory drug (NSAID) medicine in it too. If it does or if you are not sure, check with your doctor or pharmacist. Diclofenac should not be used in children; safety and effectiveness in children have not been confirmed. Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Diclofenac while you are pregnant. It is not known if Diclofenac is found in breast milk. Do not breast-feed while using Diclofenac.

Possible Side Effects

Check with your doctor if any of these most common side effects persist or become bothersome:

burning or stinging; discharge; eye redness, irritation, or itching. Seek medical attention right away if any of these severe side effects occur:

severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred or distorted vision; eye infection; eyelid swelling or redness; sensitivity to glare or light.

Diclofenac is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

Diclofenac is used to treat pain or inflammation caused by arthritis or ankylosing spondylitis. Diclofenac may also be used for purposes other than those listed in this medication guide.

Use Diclofenac as directed by your doctor.

Take Diclofenac by mouth with or without food. Ask your health care provider any questions you may have about how to use Diclofenac.

Drug Class and Mechanism

Diclofenac is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Diclofenac works by reducing hormones that cause inflammation and pain in the body.

If you miss a dose of Diclofenac, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Store Diclofenac at room temperature between 68 and 77 degrees F (20 and 25 degrees C) in a tightly closed container. Brief periods at temperatures of 59 to 86 degrees F (15 to 30 degrees C) are permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diclofenac out of the reach of children and away from pets.

Do not use Diclofenac if:

you are allergic to any ingredient in Diclofenac; you have had a severe allergic reaction (e. g. severe rash, hives, breathing difficulties, dizziness) to another NSAID (e. g. ibuprofen, naproxen, celecoxib) or aspirin. Contact your doctor or health care provider right away if any of these apply to you.

Important : Diclofenac may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Diclofenac with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Before you start any new medicine, check the label to see if it has diclofenac or another nonsteroidal anti-inflammatory drug (NSAID) medicine in it too. If it does or if you are not sure, check with your doctor or pharmacist. Diclofenac should not be used in children; safety and effectiveness in children have not been confirmed. Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Diclofenac while you are pregnant. It is not known if Diclofenac is found in breast milk. Do not breast-feed while using Diclofenac.

Possible Side Effects

Check with your doctor if any of these most common side effects persist or become bothersome:

burning or stinging; discharge; eye redness, irritation, or itching. Seek medical attention right away if any of these severe side effects occur:

severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred or distorted vision; eye infection; eyelid swelling or redness; sensitivity to glare or light.

Diclofenac is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

Fibrates drug facts, side effects and dosing, fibrafen

Fibrates

Omudhome Ogbru, PharmD

Dr. Ogbru received his Doctorate in Pharmacy from the University of the Pacific School of Pharmacy in 1995. He completed a Pharmacy Practice Residency at the University of Arizona/University Medical Center in 1996. He was a Professor of Pharmacy Practice and a Regional Clerkship Coordinator for the University of the Pacific School of Pharmacy from 1996-99.

Jay W. Marks, MD

Jay W. Marks, MD, is a board-certified internist and gastroenterologist. He graduated from Yale University School of Medicine and trained in internal medicine and gastroenterology at UCLA/Cedars-Sinai Medical Center in Los Angeles.

Daniel Lee Kulick, MD, FACC, FSCAI

Dr. Kulick received his undergraduate and medical degrees from the University of Southern California, School of Medicine. He performed his residency in internal medicine at the Harbor-University of California Los Angeles Medical Center and a fellowship in the section of cardiology at the Los Angeles County-University of Southern California Medical Center. He is board certified in Internal Medicine and Cardiology.

What are fibrates?

Fibric acid derivatives (fibrates) are a class of medication that lowers blood triglyceride levels. Fibrates lower blood triglyceride levels by reducing the liver 's production of VLDL (the triglyceride-carrying particle that circulates in the blood) and by speeding up the removal of triglycerides from the blood. Fibrates also are modestly effective in increasing blood HDL cholesterol levels ; however, fibrates are not effective in lowering LDL cholesterol.

Very high triglyceride levels (usually >1000 mg/dl) can cause pancreatitis (inflammation of the pancreas that can result in a serious illness with severe abdominal pain ). By lowering blood triglycerides. fibrates are used to prevent pancreatitis.

Fibrates are not effective in lowering LDL cholesterol ; however, when a high risk patient (see NCEP recommendations) also has high blood triglyceride or low HDL cholesterol levels, doctors may consider combining a fibrate, such as fenofibrate (Tricor ), with a statin. Such a combination will not only lower LDL cholesterol but also will lower blood triglycerides and increase HDL cholesterol levels.

Fibrates also have been used alone to prevent heart attacks especially in patients with elevated blood triglycerides and low HDL cholesterol levels. In one large study, gemfibrozil decreased the risk of heart attacks but did not affect the overall survival of persons with high cholesterol levels.

What are the side effects of fibrates?

The side effects of fibrates include nausea. stomach upset, and sometimes diarrhea. Fibrates can irritate (inflame) the liver. The liver irritation usually is mild and reversible, but it occasionally can be severe enough to require stopping the drug.

Fibrates can cause gallstones when used for several years.

Fibrates can increase the effectiveness of blood thinners, such as warfarin (Coumadin ), when both medications are used together. Thus, the dose of warfarin should be adjusted to avoid over-thinning of the blood which can lead to excessive bleeding.

Fibrates can cause muscle damage particularly when taken together with statin medications. Gemfibrozil interferes with the breakdown of certain statins (for example, simvastatin [Zocor ] or lovastatin [Mevacor. Altoprev ]), resulting in higher statin blood levels, and hence a higher likelihood of muscle toxicity from the statin. Doctors generally avoid combining a statin with fibrates because of concern over the higher risk of muscle damage with the combination. Gemfibrozil should not be combined with simvastatin and if combined with lovastatin the dose of lovastatin should not exceed 20 mg daily. However, fenofibrate does not interfere with the breakdown of statins and should be the safer fibrate to use if it is necessary to use a fibrate with a statin. Furthermore, pravastatin (Pravachol) seems to have fewer muscle toxic effects than the other statins when combined with fibrates, but the risk still exists.

Medically Reviewed by a Doctor on 9/29/2015

Quick Guide Lower Your Cholesterol, Save Your Heart

Report Problems to the Food and Drug Administration

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

Hyaluronic acid effectiveness, how it works, and drug interactions on emedicinehealth, hyalistil

What other names is Hyaluronic Acid known by?

Acide Hyaluronique, Ácido Hialurónico, Glycoaminoglycan, Glycoaminoglycane, Hyaluran, Hyaluronan. Hyaluronate de Sodium, Hyaluronate Sodium, Hylan, Sodium Hyaluronate .

What is Hyaluronic Acid?

Hyaluronic acid is a substance that is naturally present in the human body. It is found in the highest concentrations in fluids in the eyes and joints. The hyaluronic acid that is used as medicine is extracted from rooster combs or made by bacteria in the laboratory.

People take hyaluronic acid for various joint disorders, including osteoarthritis. It can be taken by mouth or injected into the affected joint by a healthcare professional.

The FDA has approved the use of hyaluronic acid during certain eye surgeries including cataract removal, corneal transplantation, and repair of a detached retina and other eye injuries. It is injected into the eye during the procedure to help replace natural fluids.

Hyaluronic acid is also used as a lip filler in plastic surgery.

Some people apply hyaluronic acid to the skin for healing wounds. burns. skin ulcers, and as a moisturizer.

There is also a lot of interest in using hyaluronic acid to prevent the effects of aging. In fact, hyaluronic acid has been promoted as a "fountain of youth." However, there is no evidence to support the claim that taking it by mouth or applying it to the skin can prevent changes associated with aging .

Likely Effective for.

Cataracts . Injecting hyaluronic acid into the eye is effective when used during cataract surgery by an eye surgeon.

Sores in the mouth . Hyaluronic acid is effective for treating mouth sores when applied to the skin as a gel.

Possibly Effective for.

Aging skin . Some research suggests that injecting a specific hyaluronic acid product (Juvéderm Ultra Plus, Allergan) into smile lines reduces the lines for up to one year.

Osteoarthritis . Hyaluronic acid might be effective for stiffness and joint pain when injected into the joint by a healthcare provider. Despite being approved by the FDA for treatment of osteoarthritis by injection, results vary. Some people report a moderate improvement in joint stiffness and pain decrease with hyaluronic acid treatment, but this is not always the case. Whether hyaluronic acid might delay or lessen progressive joint damage with long-term use is unknown.

Insufficient Evidence to Rate Effectiveness for.

Dry eye . Early research shows that applying a specific hyaluronic acid eye drop (Hyalistil) might relieve dry eye.

Eye trauma . Some research suggests that hyaluronic acid might be injected into the eye to treat detached retina or other eye injuries.

Healing skin wounds and burns . Early research suggests that applying hyaluronic acid to the skin might be helpful for treating burns and skin wounds.

More evidence is needed to rate the effectiveness of hyaluronic acid for these uses.

Natural Medicines Comprehensive Database rates effectiveness based on scientific evidence according to the following scale: Effective, Likely Effective, Possibly Effective, Possibly Ineffective, Likely Ineffective, and Insufficient Evidence to Rate (detailed description of each of the ratings).

Medical Dictionary

Enol, enol

enol

an organic compound in which one carbon of a double-bonded pair is also attached to a hydroxyl group, thus a tautomer of the ketone form. The term is also used as a prefix or infix, often italicized.

e·nol

A compound possessing a hydroxyl group (alcohol) attached to a doubly bonded (ethylenic) carbon atom (-CH=CH(OH)-); properly italicized when attached as a prefix or infix to an otherwise complete name, for example, enol pyruvate, phospho enol pyruvate; usually in equilibrium with its keto tautomer.

enol

( e?nol ) an organic compound in which one carbon of a double-bonded pair is also attached to a hydroxyl group, thus a tautomer of the ketone form; also used as a prefix or infix, often italicized.

enol

an organic compound with an alcohol or hydroxyl group directly attached (bonded) to a double bond. By transfer of the hydrogen atom from oxygen to carbon, the enol form becomes the (usually more stable) keto form. Such compounds usually exist as enol-keto tautomers.

e·nol

A compound possessing a hydroxyl group (alcohol) attached to a doubly bonded (ethylenic) carbon atom (-CH=CH(OH)-).

enol

one of two tautomeric forms of a substance, the other being the keto form; the enol is formed from the keto by migration of hydrogen from the adjacent carbon atom to the carbonyl group.

Link to this page:

Cytotoxic diacetylenic spiroketal enol ethers from Plagius flosculosus.

Hence, the first emission band observed at 385 nm (COP-UAN) and 391 nm (UAN) can be interpreted in terms of the direct emission from the intramolecularly H-bonded enol form, whereas the emission with higher intensity (480 nm and 520 nm, respectively,) can be assigned to the "de-excitation" process from the keto form of urethane anil structure appeared through tautomerization process.

3 (two nitro substituents) or higher for the enol form to be more stable than the phosphoryl form.

Mn-salen-catalyzed asymmetric oxidation of enol derivatives.

The silicone-based transformer fluid, Dow Corning 561 Silicone Transformer Liquid (DC561) was manufactured by Dow Corning Limited (Barry, South Glamorgen, UK), and the mineral oil-based transformer fluid, ENOL C, was manufactured by the Oil Rafinery Novi Sad, Yugoslavia.

One could also propose that the degradation products of such gross over-treatment might mask the underlying enol groups and prevent the close approach of the two surfaces necessary for H-bond formation.

The acquisition of Enol will significantly expand Applied's position throughout Mexico," said Todd A.

DeSimone has nearly 20 years of power transmission equipment sales experience, most recently with Enol Industrial Queretaro as General Manager.

On one hand, it could mean that the sulfate is linked to an enol in the 3 or 17 position.

A likely explanation for the consistent presence of two peaks is keto [left and right arrow] enol isomerization at the 3' position of the amino acid, MeBmt, at position one of the undecapeptide.

The chemicals that are produced at this point are flavor volatiles that include chemical compounds, such as alcohols, furans and enols. that contribute more and more to the overall caramel-like profile.

Sandia said the compounds, known as enols. were discovered using a new flame chemistry probe operated at the Advanced Light Source at Lawrence Berkeley National Laboratory.

Furosemide oral uses, side effects, interactions, pictures, warnings - dosing, furosemida

furosemide

Warnings

Furosemide is a very potent medication. Using too much of this drug can lead to serious water and salt/mineral loss. Therefore, it is important that you are closely monitored by your doctor while taking this medication. Tell your doctor right away if you become very thirsty or confused, or develop muscle cramps /weakness. See also Side Effects section.

Uses

Furosemide is used to reduce extra fluid in the body (edema ) caused by conditions such as heart failure. liver disease, and kidney disease. This can lessen symptoms such as shortness of breath and swelling in your arms, legs, and abdomen .

Furosemide is a "water pill" (diuretic) that causes you to make more urine. This helps your body get rid of extra water and salt.

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

This medication may also be used to decrease a high level of calcium in the blood (hypercalcemia).

How to use furosemide

Read the Patient Information Leaflet if available from your pharmacist before you start taking furosemide and each time you get a refill. If you have any questions, ask your doctor or pharmacist.

Take this medication by mouth as directed by your doctor, with or without food, usually once or twice daily. It is best to avoid taking this medication within 4 hours of your bedtime to prevent having to get up to urinate.

Dosage is based on your medical condition, age, and response to treatment. For children, the dose is also based on weight. Older adults usually start with a lower dose to decrease the risk of side effects. Do not increase your dose or take it more often than directed.

Take this medication regularly in order to get the most benefit from it. To help you remember, take it at the same time(s) of the day as directed. It is important to continue taking this medication even if you feel well. Most people with high blood pressure do not feel sick.

Sucralfate, cholestyramine. and colestipol can decrease the absorption of furosemide. If you are taking any of these drugs, separate the timing of each dose from furosemide by at least 2 hours.

Tell your doctor if your condition does not improve or if it worsens (for example, your blood pressure readings remain high or increase).

Side Effects

Dizziness. lightheadedness, headache. or blurred vision may occur as your body adjusts to the medication. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

To reduce the risk of dizziness and lightheadedness, get up slowly when rising from a sitting or lying position.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

This medication may cause a serious loss of body water (dehydration ) and salt/minerals. Tell your doctor right away if you have any of these unlikely but serious side effects: muscle cramps, weakness, unusual tiredness, confusion, severe dizziness, fainting. drowsiness, unusual dry mouth /thirst, nausea. vomiting. fast/irregular heartbeat. unusual decrease in the amount of urine.

Tell your doctor right away if any of these unlikely but serious side effects occur: numbness/tingling/pain/redness/swelling of the arms/legs, hearing changes (such as ringing in the ears. temporary or permanent decreased hearing/deafness ), stomach /abdominal pain. yellowing eyes /skin .

A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction. including: rash. itching /swelling (especially of the face/tongue /throat), severe dizziness, trouble breathing .

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking furosemide, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney problems, liver problems, inability to make urine, gout, lupus .

If you have diabetes, furosemide may affect your blood sugar level. Check your blood sugar level regularly as directed and share the results with your doctor. Your doctor may need to adjust your diabetes medication or diet.

Furosemide may reduce the potassium level in your blood. Your doctor may instruct you to add potassium-rich foods to your diet (such as bananas, orange juice) or prescribe potassium supplements to prevent potassium loss. Ask your doctor for more details.

This medication may make you more sensitive to the sun. Avoid prolonged sun exposure, tanning booths, and sunlamps. Use a sunscreen and wear protective clothing when outdoors.

This drug may make you dizzy or cause blurred vision. Do not drive, use machinery, or do any activity that requires alertness or clear vision until you are sure you can perform such activities safely. Limit alcoholic beverages.

Severe sweating, diarrhea, or vomiting can increase the risk of dehydration. Report prolonged diarrhea or vomiting to your doctor. Follow your doctor's instructions about the amount of fluids you can drink.

Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products).

Babies born early (premature infants) and children may be more sensitive to certain effects of this drug, such as kidney stones.

Older adults may be more sensitive to the effects of this drug, especially dizziness and water/mineral loss.

During pregnancy, this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor.

This drug passes into breast milk and may affect milk production. Consult your doctor before breast-feeding.

Interactions

See also the How to Use section.

Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage of any medicines without your doctor's approval.

Some products that may interact with this drug include: ethacrynic acid, lithium.

Check the labels on all your medicines (such as cough-and-cold products, diet aids, or NSAIDs such as ibuprofen, naproxen) because they may contain ingredients that could increase your blood pressure or worsen swelling (edema). Ask your pharmacist for more details.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: fainting, severe weakness, a severe decrease in the amount of urine.

Notes

Do not share this medication with others.

Lifestyle changes that may help this medication work better include exercising, stopping smoking, reducing stress, and changing your diet. Consult your doctor for more details.

Laboratory and/or medical tests (such as kidney tests, blood mineral levels such as potassium) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

Check your blood pressure regularly while taking this medication. Learn how to monitor your own blood pressure at home, and share the results with your doctor.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

Images

Carca; tablet, intas pharmaceuticals ltd, carca 3.125mg

CARCA 3.125mg - Tablet, Intas Pharmaceuticals Ltd

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Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. Go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about the proper use of Motrin .

Store Motrin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Motrin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal product, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

Some medicines may interact with Motrin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Motrin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Motrin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Branding & marketing agency, tivision

Strategic

Communications

We're TriVisioneers.

Integrated Marketing Communications

Leadership.

Zakia Lutfi

Arsalan Lutfi

Kamran Lutfi

Chief Marketing Officer | LinkedIn

As Co-Founder and Chief Marketing Officer of TriVision, Kamran oversees all strategic marketing communication planning and provides leadership to the marketing department by ensuring the appropriate structures, systems, competencies and values are developed. Kamran assumes overall responsibility for developing the annual marketing agenda, budgeting, outreach and business development. He has supported, led, motivated and managed teams both directly and indirectly to achieve significant sustainable business process improvements and results.

Kamran has proposed and developed new business strategies which fulfilled the organization’s vision to be an exceptional creative agency. He has modeled and developed successful partnerships with broad range of organizations such as the Northern Virginia Technology Counsel (NVTC), Dulles Regional Chamber of Commerce, Afghan-American Chamber of Commerce, and actively involved as an advisor on the board for ITT Institute.

Kamran has a BS in Marketing and a BS in Decision Science Management Information Systems (DS-MIS) from George Mason University. He speaks multiple languages including Farsi and French. He’s a world traveler, but lives in Georgetown with his “mini-me” 7 year old son.

Tabasum Lutfi

Chief Operating Officer | LinkedIn

Tabasum Lutfi is the Chief Operating Officer at TriVision. As part of the company’s overall process of management and corporate decision-making, Tabasum oversees all client relations and company operations. In addition, Tabasum leads the public relations and social media departments of the company both for TriVision and for its clients by managing campaigns across various online and digital platforms. As part of her role to build and promote the company’s brand name, Tabasum leads TriVision’s PR and business development incentives and also prepares and edits organizational publications for internal and external audiences.

Tabasum’s active involvement within various departments of TriVision – from design, web, and print, to business development and event management – indicates her ability to adapt to different skill sets and working environments, allowing her to play an integral and versatile role in TriVision’s growth and expansion as a company.

Tabasum graduated from George Mason University with a BS in Marketing and a BS in Decision Sciences and Management Information Systems with a minor in Information Technology.

Sean Powell

Sr. Production Manager | LinkedIn

Sean Powell has been working on all aspects of video production for 20 years. Prior to working at TriVision, he was employed by General Electric, The U. S. Marine Corps, and The Naval Academy. He has been working with TriVision for over 10 years and has been an important member in the growth and identity of the company.

In addition to his current responsibilities as production manager, Sean has served on projects as a director, producer, writer, videographer, editor, and/or voiceover narrator. He has served numerous times as project manager, most recently for the NCA training modules, and frequently is the contact for government clients. His broad experience on a diverse range of projects brings an important and versatile component to production environments. He holds a Bachelor of Arts degree in Film and Video from Pennsylvania State University.

Zainab Masumi

Sr. Brand Manager | LinkedIn

With over 15 years of experience in the design and marketing field, Ms. Masumi is the Senior Brand and Graphic Design Specialist at TriVision. Ms. Masumi has played a vital role for TriVision’s growth in the industry. She has had leadership roles in projects for companies such as Export-Import Bank of the United States, Pace Global, Symantec, ITC Global, MSRB and other commercial and governmental agencies.

She graduated from George Mason University with a Bachelor of Arts in Arts and Visual Technologies. Ms. Masumi’s responsibilities at TriVision have included increased brand visibility via public relations campaigns and multi-level marketing campaigns.

Chris Son

Sr. Technology Manager | LinkedIn

Chris joined TriVision in our very early years in Burke as a young college student. He has seen the growth and expansion of our brand and after being immersed in the IT field as a Network Administrator for over ten years, he rejoined TriVision to untap his creative talents. As a self-motivated and creative individual he is able to maintain projects that involve video editing, graphic design and motion graphics. His focus is in web development where he applies his extensive knowledge of PHP, ASP. NET, JS, jQuery, AJAX, XML/XSLT, CSS3, HTML5, Bootstrap. Chris is responsible for developing and overseeing custom CMS (WordPress, Joomla and Drupal) themes to build engaging and responsive websites. Accustomed to a continuously fast-paced environment, he manages multiple projects and provides clear communication between clients and employees. In his free time, Chris enjoys kickboxing and working on a billion dollar app to join Mark Cuban’s BBC.

Klaudia Strojec

Sr. Online Specialist | LinkedIn

With over ten years of experience in Web Development, Klaudia Strojec plays a leading role in TriVision’s growing web solutions team. Her extensive knowledge of different programming languages has allowed Klaudia to build elaborate and complex CMS (Content Management Systems) websites. Klaudia’s areas of expertise include: HTML, CSS, JavaScript, Java, SQL, MySql, Joomla, WordPress, Magento, Prestashop, and. NET, which have helped her to create sophisticated database-driven websites including e-commerce websites and more. With growing necessity for online presence Klaudia has focused on SEO (Search Engine Optimization) and SMM (Social Media Marketing). Having majored in Computer Science, Klaudia knows what it takes to create websites that meet all necessary requirements for current web standards. From advising clients on which framework best suits their needs, to setting-up platforms to launch the latest applications, Klaudia goes above and beyond her duties to take on each assignment seriously. She fully understands not only how to build and develop websites but she also understands how to market them to increase online presence.

Advisory board.

Senior Digital Strategist

Strategic Communications Advisor

Col. James L. Bullion (Retired)

Strategic Advisor

Jim Bullion is an experienced international executive with deep marketing, business development and management experience in a wide range of industries ranging from telecommunications to mining. He has led military and business organizations in Africa, Asia and the Middle East as well as in the US and Europe, partnering with senior leaders to build and expand effective organizations. Some of his key attributes are; relationship building and concept selling with a wide range of business, military and government leaders and organizations in multiple countries to building strong working partnerships and acceptance of value-added products and services; and value creation through product development, market development and product positioning involving market research, needs analysis and communications. He has a B. A. from Dartmouth College and his MBA from Amos Tuck School, Dartmouth College.

Ted McLaughlan

Senior Digital Strategist

Ted McLaughlan has extensive experience in formulating and implementing digital marketing & technology strategies, for long and short term marketing & communications initiatives. Ted also develops digital information and social management content & strategies for advertising, outreach, and event marketing. As an Enterprise Architect with Oracle Corporation, and a Co-Founder of KME. Digital, Ted is a Certified Systems Engineer/Solution Architect, and has a B. A. in Interdisciplinary History and Liberal Arts from the University of Virginia.

Krewasky A. Salter, PhD.

Strategic Advisor

Dr. Krewasky Salter is a former senior military officer who served more than 25 years in the United States Army, retiring as a Colonel in 2010. An Airborne Ranger, he commanded at all levels through battalion, to include deployment experience as a Battalion Commander, and served as a primary Senior Staff Officer in the Pentagon. After the military he spent nearly two years in the civilian executive arena as Chief of Staff and Strategic Capture Manager for a large government contracting firm.

Dr. Salter has a Ph. D. in History & two Masters—one in Strategic Studies-and a B. A. in Political Science. Dr. Salter is a published author and advisor and consultant for a Public Broadcasting Station Award Winning Documentary for which he was personally awarded the Congressional Black Caucus Veterans Braintrust Award for his role as Historical Adviser and Consultant. His 2014 book peaked at #2 on the publisher’s Top 10 history topics for 2014 and is an Association of the United States Army (AUSA) Book.

Douglas K. Barry

Strategic Communications Advisor

Doug Barry is a vice president at Conover + Gould Strategies Group, a Washington, DC-based consultancy specializing in strategic communications for business, non-profits, and government agencies. Barry was director of marketing and communications for the U. S. Commercial Service, the federal government’s primary export promotion organization. He also led projects in knowledge management and strategic partnerships. An award-winning video producer, Barry has written six books and hundreds of articles, many of which help U. S. businesses start or expand their international sales. In 2015, he was named International Trade Educator of the Year by NASBITE. Barry has a master’s degree from New York University and a doctorate from Columbia University.

TriVisioneers.

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etidronate disodium

Uses

Etidronate is used to treat a certain type of bone disease called Paget's disease. This disease weakens and deforms bones. Etidronate works by slowing bone loss. helping to keep your bones strong and less likely to break. It also helps reduce bone pain from this disease. This medication belongs to a class of drugs called bisphosphonates.

Etidronate is also used to prevent or treat bone problems that may occur after hip replacement surgery or spinal cord injury.

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

Etidronate may also be used to treat bone loss (osteoporosis ) if you are taking corticosteroid medications (such as prednisone ) for long periods. In addition, this medication may be used to treat a high level of calcium in the blood that may occur with some cancers.

How to use etidronate disodium

Follow these instructions very closely to make sure you absorb as much of the drug as possible and reduce the risk of injury to your esophagus. Consult your doctor or pharmacist if you have any questions.

Take this medication by mouth without food, usually once a day or as directed by your doctor. Take it on an empty stomach at least 2 hours before or 2 hours after a meal.

Take etidronate with a full glass of plain water (6 to 8 ounces, 180 to 240 milliliters). Do not take it with any other beverage. After taking etidronate, stay fully upright (sitting, standing, or walking) and do not lie down for at least 30 minutes.

Do not take etidronate at the same time as food or other medications because they may prevent its absorption. Take this medication 2 hours before or 2 hours after taking any products that contain aluminum, calcium. iron, magnesium. or zinc. Some examples include antacids, certain forms of didanosine (chewable/dispersible buffered tablets or pediatric oral solution), quinapril. vitamins /minerals, dairy products (such as milk, yogurt), and calcium - enriched juice.

The dosage is based on your medical condition, weight. and response to treatment. If stomach upset occurs, talk to your doctor about dividing your daily dose into 2 or 3 smaller doses during the day instead of taking one daily dose all at once.

For Paget's disease and bone problems after hip replacement or spinal cord injury, you will usually take this medication for 3 to 6 months. Do not take more of this medication or use it for longer than prescribed because the risk of side effects may increase.

Take this medication regularly to get the most benefit from it. To help you remember, take it at the same time(s) each day.

Side Effects

Stomach upset or diarrhea may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

Tell your doctor right away if you have any serious side effects, including: new or worsening bone/joint/muscle pain. new or unusual hip/thigh/groin pain, jaw pain. mental/mood changes, signs of infection (such as fever, persistent sore throat ).

This medication may rarely cause irritation and ulcers in your stomach or esophagus. Seek immediate medical attention if any of these serious side effects occur: new/severe/worsening heartburn. chest pain. difficult/painful swallowing, stomach/abdominal pain. black/tarry stools, vomit that looks like coffee grounds.

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction. rash. itching /swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing .

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking etidronate, tell your doctor or pharmacist if you are allergic to it; or to other bisphosphonates (such as alendronate ); or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

This medication should not be used if you have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if you have: a certain bone disorder that causes soft/painful bones (osteomalacia ).

Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney disease. inability to sit upright or stand for at least 30 minutes, difficult/painful swallowing, esophagus problems (such as esophageal stricture, achalasia ), stomach/intestinal problems (such as heartburn. ulcers, colitis ), low level of calcium in the blood .

Some people taking etidronate may have serious jawbone problems. Your doctor should check your mouth before you start this medication. Tell your dentist that you are taking this medication before you have any dental work done. To help prevent jawbone problems, have regular dental exams and learn how to keep your teeth and gums healthy. If you have jaw pain. tell your doctor and dentist right away.

Before having any surgery (especially dental procedures), tell your doctor and dentist about this medication and all other products you use (including prescription drugs, nonprescription drugs, and herbal products). Your doctor or dentist may tell you to stop taking etidronate before your surgery. Ask for specific instructions about stopping or starting this medication.

Caution is advised if you are pregnant or planning to become pregnant in the future. This medication may stay in your body for many years. Its effects on an unborn baby are not known. Discuss the risks and benefits with your doctor before starting treatment with this medication.

It is not known if this medication passes into breast milk, and the effect on a nursing infant is unknown. Consult your doctor before breast-feeding.

Interactions

See also the How to Use section.

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with your doctor or pharmacist first.

This medication may affect the results of certain lab tests (bone imaging tests). Make sure laboratory personnel and all your doctors know you use this drug.

This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: muscle spasms, mental/mood changes.

Notes

Do not share this medication with others.

Lifestyle changes that help promote healthy bones include increasing weight-bearing exercise, stopping smoking, limiting alcohol, and eating well-balanced meals that contain adequate calcium and vitamin D. You may also need to take calcium and vitamin D supplements. Consult your doctor for specific advice.

Laboratory and/or medical tests (such as X-rays, calcium and other blood mineral levels, kidney function tests) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

Missed Dose

If you miss a dose, take it as soon as you remember, following the dose-timing instructions in the How to Use section. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature between 59-86 degrees F (15-30 degrees C) away from light and moisture. Do not store in the bathroom. Keep all medicines away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

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Tenormin (Cardaten)

Tenormin is used to treat angina (chest pain) and hypertension (high blood pressure). Tenormin is used for decreasing death due to heart problems after a heart attack. Tenormin is a beta-blocker. Exactly how Tenormin works to decrease heart problems after a heart attack is not known.

Use Tenormin as directed by your doctor.

Do not take Tenormin in larger amounts or for longer than recommended by your doctor.

Take Tenormin with a full glass of water.

Take Tenormin at the same time every day.

Do not skip doses or stop taking Tenormin without first talking to your doctor. Stopping suddenly may make your condition worse.

To be sure this medication is helping your condition, your blood pressure will need to be checked on a regular basis. It is important that you not miss any scheduled visits to your doctor.

If you need to have any type of surgery, tell the surgeon that you are using Tenormin. You may need to briefly stop using Tenormin before having surgery.

Tenormin is only part of a complete program of treatment for hypertension that may also include diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely if you are being treated for hypertension.

Hypertension often has no symptoms, so you may not even feel that you have high blood pressure. Continue using this medicine as directed, even if you feel well. You may need to use blood pressure medication for the rest of your life.

Ask your health care provider any questions you may have about how to use Tenormin.

Store Tenormin at room temperature away from moisture and heat. Keep Tenormin out of the reach of children and away from pets.

Active Ingredient: Atenolol.

Do NOT use Tenormin if:

you are allergic to any ingredient in Tenormin

you have a very slow heartbeat, heart block, uncontrolled heart failure, shock caused by serious heart problems, or low blood pressure after a heart attack

you have an untreated adrenal gland tumor (pheochromocytoma)

you are taking mibefradil.

Contact your doctor or health care provider right away if any of these apply to you.

Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of any severe allergic reaction

if you have a history of lung or breathing problems (eg, asthma, chronic bronchitis, chronic obstructive pulmonary disease [COPD], emphysema), heart problems (eg, heart failure, conduction problems, left ventricle problems), blood vessel problems, diabetes, kidney problems, an adrenal gland tumor, or an overactive thyroid.

Some medicines may interact with Tenormin. Tell your health care provider if you are taking any of the following medicines.

Clonidine because the risk of severe high blood pressure may be increased

Mefloquine because the risk of irregular heartbeat may be increased

Amiodarone, calcium channel blockers (eg, diltiazem, verapamil), catecholamine-depleting medicines (eg, reserpine), digoxin, disopyramide, flecainide, ketanserin, mibefradil, or quinidine because they may increase the risk of Tenormin's side effects

Indomethacin or phenylpropanolamine because it may decrease Tenormin's effectiveness

Bupivacaine, lidocaine, or quinazolines (eg, alfuzosin) because the risk of their side effects may be increased by Tenormin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Tenormin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Tenormin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Tenormin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Tenormin may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

Tell your doctor or dentist that you take Tenormin before you receive any medical or dental care, emergency care, or surgery.

Tenormin may reduce the amount of blood that flows to your feet and hands. This may cause them to feel cold and make you more sensitive to the cold. Dress warmly in cold weather. Be careful when you are out in the cold for long periods of time. Ask you doctor for more information.

If you have a history of any severe allergic reaction, talk with your doctor. You may be at risk for an even more severe allergic reaction if you come into contact with the substance that caused your allergy. Some medicines used to treat severe allergies may also not work as well while you are using Tenormin.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

Diabetes patients - Tenormin may hide signs of low blood sugar such as a rapid heartbeat. Other symptoms, such as sweating, may still occur. Check your blood sugar levels regularly. Ask your doctor before you change the dose of your diabetes medicine.

Check your blood pressure and pulse regularly, as directed by your doctor. Ask your doctor or pharmacist for help if you are unsure how to properly measure your blood pressure or pulse.

Lifestyle changes may also help reduce your blood pressure. Talk with your doctor about appropriate diet and exercise programs that may be helpful to you.

Lab tests, including blood pressure and heart function tests, may be performed while you use Tenormin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Tenormin with caution in the elderly; they may be more sensitive to its effects, especially dizziness.

Tenormin should be used with extreme caution in children; safety and effectiveness in children have not been determined.

Pregnancy and breast-feeding: Tenormin has been shown to cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Tenormin while you are pregnant. Tenormin is found in breast milk. If you are or will be breast-feeding while you use Tenormin, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Cold fingers and toes; diarrhea; dizziness; drowsiness; nausea; tiredness or weakness.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blue fingernails, toenails, or palms; decreased sexual ability; fainting; mental or mood problems; persistent dizziness or lightheadedness; shortness of breath; sudden, unusual weight gain; swelling of hands, ankles, or feet; unusual bruising or bleeding; unusually slow heartbeat.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

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Amlip (amlodipine besilate) - 10mg (10 tablets), amlip 10mg

Amlip (Amlodipine Besilate) - 10mg (10 Tablets)

Generic Name. Amlodipine Besylate |

About Amlip. Amlopres (Amlodipine Besilate) is used to lower high blood pressure (hypertension).

How to use Amlip

Amlopres (Amlodipine Besilate) is used to lower high blood pressure (hypertension). There are usually no symptoms of hypertension. The only way of knowing that you have hypertension is to have your blood pressure checked on a regular basis. If high blood pressure is not treated it can lead to serious health problems.

Amlopres (Amlodipine Besilate) belongs to a group of medicines called calcium channel blockers or calcium ion antagonists. They work by widening your blood vessels, making it easier for your heart to pump blood around the body and help increase the supply of blood and oxygen to your heart. Calcium channel blockers do not change the amount of calcium in your blood or bones.

Amlopres (Amlodipine Besilate) is also used to treat angina pectoris. Angina is a pain or uncomfortable feeling in the chest, often spreading to the arms or neck, and sometimes to the shoulders and back. The pain of angina is due to a shortage of oxygen to the heart.

Amlip Dosage

Amlopres (Amlodipine Besilate) is provided as tablets for oral administration. However, a full medical consultation is required prior to beginning treatment. This is so that your physician can determine the correct dosage and suitability of this drug. Only take the amount of medicine that your physician tells you to take.

Amlip Side Effects

Amlopres (Amlodipine Besilate) may cause side effects. You are advised to discuss the risk of this with your physician prior to commencing treatment. Some side effects may be serious and require immediate medical attention.

Amlip Precautions

If you have an allergic or hypersensitive reaction, seek emergency medical attention. Possible symptoms include difficulty breathing, difficulty swallowing, swelling, chest tightness, skin rashes, and hives.

Amlopres (Amlodipine Besilate) should only be used as instructed and prescribed by your physician or pharmacist. Do not alter your dosage unless specifically instructed to do so by either of the above. Dosage and usage often depends on the severity of the condition, as well as the patient`s medical history and current health condition.

Before you begin using this medication, ensure your physician is aware of the following:

If you are pregnant or breastfeeding.

If you have any allergies.

If you have any other illnesses, disorders, or medical conditions.

If you are using any other drugs or medication.

If you are using any vitamins or supplements.

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Bayer and monsanto to create a global leader in agriculture - bayer news, bayer

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Wednesday - September 14, 2016

Bayer and Monsanto to Create a Global Leader in Agriculture

Realizes a shared vision of integrated agricultural offerings, delivering enhanced solutions for growers and creates a leading innovation engine for the next generation of farming / USD 128 per share in all-cash transaction, represents 44 percent premium to Monsanto shareholders and an aggregate value of USD 66 billion / Significant value creation with expected annual synergies of approximately USD 1.5 billion after year three; plus additional synergies from integrated solutions in future years / Bayer shareholders expected to benefit from accretion to core EPS in the first full year after closing and double-digit percentage accretion in the third full year / Committed to retaining strong presence in the U. S. with the combined business’ global Seeds & Traits and North American commercial headquarters in St. Louis

download Werner Baumann (left), CEO of Bayer AG, and Hugh Grant, Chairman and Chief Executive Officer of Monsanto.

Leverkusen / St. Louis, September 14, 2016 – Bayer and Monsanto today announced that they signed a definitive merger agreement under which Bayer will acquire Monsanto for USD 128 per share in an all-cash transaction. Monsanto’s Board of Directors, Bayer’s Board of Management and Bayer’s Supervisory Board have unanimously approved the agreement. Based on Monsanto’s closing share price on May 9, 2016, the day before Bayer’s first written proposal to Monsanto, the offer represents a premium of 44 percent to that price.

“We are pleased to announce the combination of our two great organizations. This represents a major step forward for our Crop Science business and reinforces Bayer’s leadership position as a global innovation driven Life Science company with leadership positions in its core segments, delivering substantial value to shareholders, our customers, employees and society at large,” said Werner Baumann, CEO of Bayer AG.

“Today’s announcement is a testament to everything we’ve achieved and the value that we have created for our stakeholders at Monsanto. We believe that this combination with Bayer represents the most compelling value for our shareowners, with the most certainty through the all-cash consideration,” said Hugh Grant, Chairman and Chief Executive Officer of Monsanto.

Enhanced Solutions for Growers

This transaction brings together two different, but highly complementary businesses. The combined business will benefit from Monsanto’s leadership in Seeds & Traits and Climate Corporation platform along with Bayer’s broad Crop Protection product line across a comprehensive range of indications and crops in all key geographies. As a result, growers will benefit from a broad set of solutions to meet their current and future needs, including enhanced solutions in seeds and traits, digital agriculture, and crop protection.

The combination also brings together both companies’ leading innovation capabilities and R&D technology platforms, with an annual pro-forma R&D budget of approximately EUR 2.5 billion. Over the mid to long-term, the combined business will be able to accelerate innovation and provide customers with enhanced solutions and an optimized product suite based on analytical agronomic insight supported by Digital Farming applications. These are expected to result in significant and lasting benefits for farmers: from improved sourcing and increased convenience to higher yield, better environmental protection and sustainability.

“The agriculture industry is at the heart of one of the greatest challenges of our time: how to feed an additional 3 billion people in the world by 2050 in an environmentally sustainable way. It has been both companies’ belief that this challenge requires a new approach that more systematically integrates expertise across Seeds, Traits and Crop Protection including Biologicals with a deep commitment to innovation and sustainable agriculture practices,” said Liam Condon, member of the Board of Management of Bayer AG and head of the Crop Science Division.

“We are entering a new era in agriculture – one with significant challenges that demand new, sustainable solutions and technologies to enable growers to produce more with less. This combination with Bayer will deliver just that – an innovation engine that pairs Bayer’s crop protection portfolio with our world-class seeds and traits and digital agriculture tools to help growers overcome the obstacles of tomorrow. Together Monsanto and Bayer will build on our proud tradition and respective track records of innovation in the agriculture industry, delivering a more comprehensive and broader set of solutions to growers,” said Grant.

Pro forma sales of the combined agricultural business amounted to EUR 23 billion in calendar year 2015. The combined company will be well positioned to participate in the agricultural industry with significant long-term growth potential. Beyond the attractive long term value creation potential of the combination, Bayer expects the transaction to provide its shareholders with accretion to core EPS (earnings per share) in the first full year after closing and a double-digit percentage accretion in the third full year. Bayer has confirmed sales and cost synergies assumptions in due diligence and expects annual EBITDA contributions from total synergies of approximately USD 1.5 billion after year three, plus additional synergies from integrated solutions in future years.

Financing and Closing Conditions

Bayer intends to finance the transaction with a combination of debt and equity. The equity component of approximately USD 19 billion is expected to be raised through an issuance of mandatory convertible bonds and through a rights issue with subscription rights. Bridge financing for USD 57 billion is committed by BofA Merrill Lynch, Credit Suisse, Goldman Sachs, HSBC and JP Morgan.

Bayer has a proven track record of disciplined deleveraging after large acquisitions and believes that the strong cash flows of the combined business will contribute to improving its financial profile. Bayer targets an investment grade credit rating post-closing and is committed to the single “A” credit rating category over the long-term.

The acquisition is subject to customary closing conditions, including Monsanto shareholder approval of the merger agreement and receipt of required regulatory approvals. Closing is expected by the end of 2017. The companies will work diligently with regulators to ensure a successful closing. In addition, Bayer has committed to a USD 2 billion reverse antitrust break fee, reaffirming its confidence that it will obtain the necessary regulatory approvals.

Headquarters and Employees

The combined agriculture business will have its global Seeds & Traits and North American commercial headquarters in St. Louis, Missouri, its global Crop Protection and overall Crop Science headquarters in Monheim, Germany, and an important presence in Durham, North Carolina, as well as many other locations throughout the U. S. and around the world. The Digital Farming activities for the combined business will be based in San Francisco, California.

“This combination is a great opportunity for employees, who will be at the forefront of innovation in our sector. This transaction also enhances Bayer’s strong commitment to the U. S. building on our 150-year history with operations across 25 states employing more than 12,000 people in the country. I am convinced that Monsanto will flourish as part of one of the most respected and trusted companies in the world,” said Baumann.

Bayer has extensive experience in successfully integrating acquisitions from a business, geographic and cultural perspective, and remains committed to its strong culture of innovation, sustainability and social responsibility.

Advisors to the Transaction

BofA Merrill Lynch and Credit Suisse are acting as lead financial advisors and structuring banks to Bayer in addition to providing committed financing for the transaction; Rothschild has been retained as an additional financial advisor to Bayer. Bayer’s legal advisors are Sullivan & Cromwell LLP (M&A) and Allen & Overy LLP (Financing).

Morgan Stanley & Co. and Ducera Partners are acting as financial advisors, and Wachtell, Lipton, Rosen & Katz is acting as legal advisor to Monsanto.

Further information is available on the internet at: www. advancingtogether. com

- Statements of Werner Baumann and Hugh Grant as video and script (until approx. 2:30 p. m. CEST / 8:30 a. m. EDT) - Slides for the Investor Conference Call (until approx. 2:00 p. m. CEST / 8:00 a. m. EDT) - Live webcast of the Investor Conference Call (from approx. 2:00 p. m. CEST / 8:00 a. m. EDT) - Slides for the Media Conference Call (until approx. 3:30 p. m. CEST / 9:30 a. m. EDT) - Speech and embedded slides for the Media Conference Call (from approx. 3:30 p. m. CEST / 9:30 a. m. EDT) - Live webcast of the Media Conference Call (from approx. 3:30 p. m. CEST / 9:30 a. m. EDT)

Transcripts and audio recordings of all conference calls will be available afterwards.

Print-quality photos can be downloaded on the internet at: www. news. bayer. com

TV and multimedia editors can download or order updated film footage about Bayer free of charge at: www. tv-footage. bayer. com

Bayer: Science For A Better Life

Bayer is a global enterprise with core competencies in the Life Science fields of health care and agriculture. Its products and services are designed to benefit people and improve their quality of life. At the same time, the Group aims to create value through innovation, growth and high earning power. Bayer is committed to the principles of sustainable development and to its social and ethical responsibilities as a corporate citizen. In fiscal 2015, the Group employed around 117,000 people and had sales of EUR 46.3 billion. Capital expenditures amounted to EUR 2.6 billion, R&D expenses to EUR 4.3 billion. These figures include those for the high-tech polymers business, which was floated on the stock market as an independent company named Covestro on October 6, 2015. For more information, go to www. bayer. com.

About Monsanto Company

Monsanto is committed to bringing a broad range of solutions to help nourish our growing world. We produce seeds for fruits, vegetables and key crops – such as corn, soybeans, and cotton – that help farmers have better harvests while using water and other important resources more efficiently. We work to find sustainable solutions for soil health, help farmers use data to improve farming practices and conserve natural resources, and provide crop protection products to minimize damage from pests and disease. Through programs and partnerships, we collaborate with farmers, researchers, nonprofit organizations, universities and others to help tackle some of the world’s biggest challenges. To learn more about Monsanto, our commitments and our more than 20,000 dedicated employees, please visit: discover. monsanto. com and monsanto. com. Follow our business on Twitter® at twitter. com/MonsantoCo on the company blog, Beyond the Rows® at monsantoblog. com or subscribe to our News Release RSS Feed.

Cautionary Statements Regarding Forward-Looking Information Certain statements contained in this communication may constitute “forward-looking statements.” Actual results could differ materially from those projected or forecast in the forward-looking statements. The factors that could cause actual results to differ materially include the following: the risk that Monsanto Company’s (“Monsanto”) stockholders do not approve the transaction; uncertainties as to the timing of the transaction; the possibility that the parties may be unable to achieve expected synergies and operating efficiencies in the merger within the expected timeframes or at all and to successfully integrate Monsanto’s operations into those of Bayer Aktiengesellschaft (“Bayer”); such integration may be more difficult, time-consuming or costly than expected; revenues following the transaction may be lower than expected; operating costs, customer loss and business disruption (including, without limitation, difficulties in maintaining relationships with employees, customers, clients or suppliers) may be greater than expected following the transaction; the retention of certain key employees at Monsanto; risks associated with the disruption of management’s attention from ongoing business operations due to the transaction; the conditions to the completion of the transaction may not be satisfied, or the regulatory approvals required for the transaction may not be obtained on the terms expected or on the anticipated schedule; the parties’ ability to meet expectations regarding the timing, completion and accounting and tax treatments of the merger; the impact of indebtedness incurred by Bayer in connection with the transaction and the potential impact on the rating of indebtedness of Bayer; the effects of the business combination of Bayer and Monsanto, including the combined company’s future financial condition, operating results, strategy and plans; other factors detailed in Monsanto’s Annual Report on Form 10-K filed with the U. S. Securities and Exchange Commission (the “SEC”) for the fiscal year ended August 31, 2015 and Monsanto’s other filings with the SEC, which are available at http://www. sec. gov and on Monsanto’s website at www. monsanto. com ; and other factors discussed in Bayer’s public reports which are available on the Bayer website at www. bayer. com. Bayer and Monsanto assume no obligation to update the information in this communication, except as otherwise required by law. Readers are cautioned not to place undue reliance on these forward-looking statements that speak only as of the date hereof.

Additional Information and Where to Find It This communication relates to the proposed merger transaction involving Monsanto and Bayer. In connection with the proposed merger, Monsanto and Bayer intend to file relevant materials with the SEC, including Monsanto’s proxy statement on Schedule 14A (the “Proxy Statement”). This communication does not constitute an offer to sell or the solicitation of an offer to buy any securities or a solicitation of any vote or approval, and is not a substitute for the Proxy Statement or any other document that Monsanto may file with the SEC or send to its stockholders in connection with the proposed merger. STOCKHOLDERS OF MONSANTO ARE URGED TO READ ALL RELEVANT DOCUMENTS FILED WITH THE SEC, INCLUDING THE PROXY STATEMENT, WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT THE PROPOSED TRANSACTION. Investors and security holders will be able to obtain the documents (when available) free of charge at the SEC’s web site, http://www. sec. gov. and Monsanto’s website, www. monsanto. com. and Monsanto stockholders will receive information at an appropriate time on how to obtain transaction-related documents for free from Monsanto. In addition, the documents (when available) may be obtained free of charge by directing a request to Corporate Secretary, Monsanto Company, 800 North Lindbergh Boulevard, St. Louis, Missouri 63167, or by calling (314) 694-8148.

Participants in Solicitation Monsanto, Bayer and their respective directors and executive officers may be deemed to be participants in the solicitation of proxies from the holders of Monsanto common stock in respect of the proposed transaction. Information about the directors and executive officers of Monsanto is set forth in the proxy statement for Monsanto’s 2016 annual meeting of stockholders, which was filed with the SEC on December 10, 2015, and in Monsanto’s Annual Report on Form 10-K for the fiscal year ended August 31, 2015, which was filed with the SEC on October 29, 2015. Other information regarding the participants in the proxy solicitation and a description of their direct and indirect interests, by security holdings or otherwise, will be contained in the Proxy Statement and other relevant materials to be filed with the SEC in respect of the proposed transaction when they become available.

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Keftab 500mg, keftab 500mg

Keftab is a cephalosporin antibiotic. It kills, fights and stops the growth of some bacteria in the body. This medicine is used to treat many kinds of infections including upper respiratory infections, ear infections, skin infections, and urinary tract infections. It will not work for colds, flu, or other viral infections.

Dosage and direction Take the medication exactly as it was prescribed for you by your doctor. Do not take a dose larger or take it for longer than recommended by your doctor. Follow the instructions on your prescription schedule. Take Keftab with a full glass of water. Dissolve the Keftab dispersible tablet in a small amount of water, about 2 teaspoonfuls. Stir this mixture and drink all of it right away. To make sure you get the entire dose, add a little more water to the same glass, swirl gently and drink right away. Do not swallow or chew a dispersible tablet. Take Keftab for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated but do not stop taking it. Keftab will not treat a viral infection such as the common cold or flu. Keftab can cause you to have unusual results with certain medical tests. Tell any doctor who treats you that you are using Keftab.

Do not use this medication if you are allergic to cephalexin, or to similar antibiotics (Ceclor, Ceftin, Cefzil, Duricef, Fortaz, Omnicef, Spectracef, Suprax, and others). Before using Keftab, tell your doctor if you are allergic to any drugs (especially penicillins), or if you have kidney or liver disease, a stomach or intestinal disorder such as colitis, diabetes, or if you are malnourished.

Contraindications Allergy to cephalexin, or to similar antibiotics (Ceclor, Ceftin, Cefzil, Duricef, Fortaz, Omnicef, Spectracef, Suprax, and others), to penicillins, kidney or liver disease, a stomach or intestinal disorder such as colitis, diabetes, or if you are malnourished, pregnant or trying to get pregnant and are breast-feeding.

Possible side effects Get emergency medical help if you have any of these signs of an allergy: hives, difficulty breathing, swelling of your face, lips, tongue, or throat. You should call your doctor immediately if you experience diarrhea that is watery or bloody, seizure (convulsions), fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, hallucinations (seeing things that are not there) or urinating less than usual or not at all. Next side effects are less serious and they may include mild nausea, vomiting, diarrhea, dizziness, tired feeling, joint pain or vaginal itching or discharge.

Drug interactions Tell your doctor if you are using some of the drugs such as a blood thinner such as warfarin (Coumadin), metformin (Fortamet, Glucophage, Riomet, Actoplus, Avandamet, Metaglip) or probenecid (Benemid). Also do not forget to tell your doctor about all the prescription and over-the-counter medications you use including vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor by yourself.

Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regular scheduled time. Do not take extra medicine to make up the missed dose.

Overdose Seek emergency medical attention if you think you have used too much of this medicine. Overdose symptoms may include nausea, vomiting, stomach pain, diarrhea, and blood in your urine.

Storage Store the tablets and capsules at room temperature. Keep it away from moisture and heat. Throw away any unused medication after 14 days.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Cephalexin is attributed as antibiotic of cephalosporins group which acts against bacteria preventing formation of their cell walls. It is enough resistant to penicillinases of gram positive microorganisms but can be destroyed by beta-lactamases of gram negative ones. It shows broad spectrum activity against gram positive microorganisms such as Staphylococcus, Staphylococcus epidermidis; Streptococcus, Corynebacterium diphtheriae, Clostridium, Actinomyces israelii, Bacillus anthracis, gram negative microorganisms like Escherichia coli, Klebsiella, Proteus mirabilis, Neisseria gonorrhoeae, Neisseria meningitidis, Shigella, Salmonella. Common infections that are treated with Cephalexin include infections of the middle ear, tonsils, throat, larynx (laryngitis), bronchi (bronchitis) and pneumonia as well as in urinary tract, skin, and bones.

Dosage and directions The dose of Cephalexin for adults is 1 to 4 grams in divided doses. The interval between doses may be 6 or 12 hours depending on the infection.

Precautions Before using Cephalexin, tell your doctor if you are allergic to any drugs (especially penicillins), have kidney or liver disease, a stomach or intestinal disorder such as colitis, and diabetes.

Contraindications Hypersensitivity to Cephalexin, cephalosporins (Ceclor, Duricef, Omnicef, Spectracef, Suprax, Cefzil, Fortaz, Ceftin) and beta-lactamase antibiotics. Cautiousness should be exercised in patients with kidney disorder, pseudomembranous colitis, pregnancy, breastfeeding and babies younger than 6 month.

Possible side effect

Most common side effects may include signs of allergy (hives, rash, swelling of face and tongue), seizure, fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, fever, hallucinations, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, decreased or absent urination. In case of serious and persistent side effects listed above seek immediate medical help.

Drug interaction Inform your doctor about all medications you take and especially about live vaccines, probenecid. Cephalexin may decrease the effectiveness of combination-type contraceptive pills. This medication is able to show false positive results with certain diabetic urine testing products. Cephalexin increases effects of indirect anticoagulants, polphenilbutazone, furocemide. Salicylates and indomethacin slow excretion of cephalolexin by kidneys. Medications decreasing secretion in renal tubules increase concentration of the medication blood serum and slow down its excretion.

Missed dose If you missed a dose take it as soon as you remember. If it is almost time of your next dose just skip it and return to your regular schedule. Never double the dose of this medication.

Overdose In case of serious and persistent symptoms of nausea, vomiting, stomach pain, diarrhea, and blood in your urine consult your doctor about medical attention.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Asmol cfc-free inhaler, asmol

Asmol Inhaler CFC-Free

contains the active ingredient salbutamol

Consumer Medicine Information

What is in this leaflet

This leaflet answers some common questions about Asmol inhaler.

It does not contain all of the available information. It does not take the place of talking to your doctor or pharmacist.

All medicines have benefits and risks. Your doctor has weighed the risks of you taking Asmol inhaler against the benefits they expect it will have for you.

If you have any concerns about taking this medicine, talk to your doctor or pharmacist.

This medicine is only part of a general plan to help you manage your asthma or other chest conditions. You should discuss this plan with your doctor. Ask your doctor to check your treatment regularly.

Keep this leaflet with your medicine. You may need to read it again.

What Asmol inhaler is used for

Asmol inhaler is used to help treat the symptoms of:

asthma

bronchitis

emphysema

other breathing problems.

In people who have difficulty breathing during exercise, Asmol inhaler may also be used before exercise to keep the air passages open.

Asmol inhaler contains a medicine called salbutamol. Each dose (puff) contains 100 micrograms of salbutamol. There are 200 doses in each Asmol inhaler.

Salbutamol belongs to a group of medicines called bronchodilators or beta-2 agonists. When your chest is tight or when you are wheezing, Asmol is inhaled into the lungs and works rapidly to open up the air passages in your lungs, helping you breathe more easily. Asmol inhaler gives fast relief from your chest symptoms and is often called a "reliever" medicine. You may also know it as a "reliever puffer".

Some people start wheezing or their chest starts to feel tight when they exercise. This is called exercise-induced asthma. If you have exercise-induced asthma, your doctor may tell you to take one or two puffs of your Asmol inhaler before you exercise. This can help prevent the symptoms of exercise-induced asthma.

Asmol inhaler helps to control your condition but does not cure it.

Your doctor may have prescribed Asmol inhaler for another reason. Ask your doctor if you have any questions about why Asmol inhaler has been prescribed for you.

There is no evidence that Asmol inhaler is addictive.

Before you use Asmol inhaler

When you must not use it

Do not use Asmol inhaler if you are allergic to medicines containing salbutamol or any of the ingredients listed at the end of this leaflet.

Some of the symptoms of an allergic reaction may include skin rash, itching or hives, swelling of the face, lips or tongue which may cause difficulty in swallowing or breathing, wheezing or shortness of breath.

Do not use your Asmol inhaler to control miscarriage or premature labour.

Do not use this medicine after the expiry date printed on the pack or if the packaging is torn or shows signs of tampering. If it has expired or is damaged, return it to your pharmacist for disposal.

Before you start to use it

Tell your doctor if you are allergic to any other medicines, foods, dyes or preservatives.

Tell your doctor if you are pregnant or plan to become pregnant.

The ingredients of Asmol inhaler are known to cross the placenta during pregnancy. Your doctor will discuss the risks and benefits of using Asmol inhaler during pregnancy.

It is important that asthma is managed well during pregnancy and you should not stop taking your medicine without asking your doctor.

Tell your doctor if you are breastfeeding or wish to breastfeed. Your doctor will discuss the risks and benefits of using Asmol inhaler when breastfeeding.

Tell your doctor if you have any medical conditions, especially the following:

high blood pressure

heart problems

liver problems

kidney problems

thyroid conditions

diabetes.

Tell your doctor if you had to stop taking this or any other asthma medicine for any reason. Your doctor may want to take special care if you have any of these conditions.

If you have not told your doctor about any of the above, tell them before you start using Asmol inhaler.

Taking other medicines

Tell your doctor if you are taking any other medicines, including any that you buy without a prescription from a pharmacy, supermarket or health food shop.

Some medicines may be affected by Asmol inhaler, or may affect how well it works. These include:

beta-blockers, medicines used to treat high blood pressure or heart conditions

some cough and cold preparations

some weight reducing medicines

some medicines used to treat depression or other mood disorders.

Your doctor can tell you what to do if you are taking any of these medicines.

If you are not sure whether you are taking any of these medicines, check with your doctor or pharmacist. Your doctor and pharmacist have more information on medicines to be careful with or avoid while using Asmol inhaler.

How to use Asmol inhaler

How much to use

The usual Asmol inhaler dose is one or two puffs every four hours if needed. Your doctor may advise you to take a different dose. This depends on your condition and whether or not you are taking any other medicine.

Elderly patients may need smaller doses. If you have an Asthma Action Plan that you have agreed with your doctor, follow it closely at all times.

Follow all directions given to you by your doctor and pharmacist carefully.

How to use it

Instructions on how to use Asmol inhaler are included in the pack.

Read these instructions carefully before using Asmol inhaler. The pharmacist's label will usually tell you how many puffs to take and how often to use your Asmol inhaler. If you are not sure, ask your doctor or pharmacist.

Children may require adult supervision when using their Asmol inhaler.

If your Asmol inhaler is new, or if you have not used it for 5 days or more, point the mouthpiece away from you and spray two puff into the air before using it.

This will ensure that your inhaler will work properly.

You should visit your doctor or pharmacist regularly to check that you are using your Asmol inhaler in the right way. If you are not breathing the medicine in correctly, the medicine may not be helping you as much as it could be.

If you have trouble using your Asmol inhaler, talk to your doctor or pharmacist.

You may find using a spacer device with your Asmol inhaler helpful.

To use a spacer device, fit your Asmol inhaler into the spacer, spray one puff of Asmol into the spacer and then slowly breathe in as far as possible. Hold your breath for as long as comfortable, before breathing out slowly. Repeat this for each puff of your Asmol inhaler.

Most people will benefit from the use of a spacer device with their Asmol inhaler.

Use of a spacer will help more of the drug to reach your lungs and reduce the amount of drug deposited in the mouth and back of the throat. This will help to lessen your chance of getting local side effects such as mouth and throat irritation and hoarse voice.

Your pharmacist or doctor can help you with more information about spacer devices.

If you forget to use it

If you are using this medicine regularly and you miss a dose, take it as soon as you remember.

Do not take a double dose to make up for the dose you missed.

If you are not sure what to do, ask your doctor or pharmacist.

If you have any questions about this, check with your doctor or pharmacist.

If you use too much (overdose)

Immediately telephone your doctor or the Poisons Information Centre (telephone 13 11 26) for advice, or go to Accident and Emergency at the nearest hospital, if you think you or anyone else may have taken too much Asmol inhaler. Do this even if there are no signs of discomfort or poisoning. You may need urgent medical attention.

If you take too many puffs of your Asmol inhaler, you may have a fast heart beat, feel shaky or have a headache. You may also have increased acid in the blood, which may cause an increased rate of breathing. These symptoms are usually mild side effects of using Asmol inhaler. However, if they are severe or do not go away, it may be that you have used too much Asmol.

While you are using Asmol inhaler

Things you must do

IMPORTANT: If your breathing suddenly becomes more difficult just after using Asmol inhaler, tell your doctor immediately or go to Accident and Emergency at the nearest hospital.

Your doctor may tell you to take extra puffs of your Asmol inhaler if your chest condition suddenly gets worse. If you take extra puffs and do not get relief, tell your doctor immediately.

Tell your doctor as soon as possible if:

your Asmol inhaler does not help your breathing as much as usual

the effect of your Asmol does not last as long as usual or lasts less than 3 hours

you need more puffs than usual of Asmol to get relief.

These may be signs that your chest condition is getting worse.

Your doctor may decide to add another medicine to your treatment if your Asmol puffer is not having the same effect as before.

Make sure you keep your Asmol inhaler with you at all times.

Before starting any new medicine, tell your doctor or pharmacist that you are using Asmol inhaler.

Tell all the doctors, dentists and pharmacists who are treating you that you are using Asmol inhaler.

If you are going to have surgery, tell the surgeon or anaesthetist that you are taking this medicine. It may affect other medicines used in surgery.

If you become pregnant while taking Asmol inhaler, tell your doctor.

Visit your doctor regularly so they can check on your condition. Your doctor or pharmacist may recommend the use of a peak flow meter to help monitor your condition at home.

Things you must not do

Do not stop using Asmol inhaler or lower the dose without checking with your doctor.

Do not let yourself run out of medicine over the weekend or on holidays.

Do not take any other medicines for your breathing problems without checking with your doctor.

Do not use Asmol inhaler to treat any other conditions unless your doctor tells you to.

Do not give Asmol inhaler to anyone else, even if they have the same condition as you.

Things to be careful of

Be careful driving or operating machinery until you know how Asmol inhaler affects you. Asmol inhaler may cause fine tremors, dizziness or lightheadedness in some people. If any of these occur, do not drive, operate machinery or do anything else that could be dangerous.

Side effects

Tell your doctor or pharmacist as soon as possible if you do not feel well while you are using Asmol inhaler. Like all other medicines, Asmol inhaler may have unwanted side effects in some people. Most of the side effects will be minor and temporary, but sometimes they are serious. You may need medical treatment if you get some of the side effects.

Do not be alarmed by this list of possible side effects. You may not experience any of them.

Ask your doctor or pharmacist to answer any questions you may have.

Tell your doctor if you notice any of the following and they worry you:

muscle cramps

mouth or throat irritation

headache

trembling or shakiness, especially of the hands

fast heart beat

nausea or feeling sick

unusual feelings of warmth

restlessness in children.

Tell your doctor immediately if you notice any of the following:

skin rash, hives or itching

irregular heart beat, palpitations.

Tell your doctor immediately or go to Accident and Emergency at the nearest hospital if you notice any of the following:

swelling of the face, lips, mouth, tongue or throat which may cause difficulty in swallowing or breathing

severe dizziness, fainting or collapse

increased wheezing or difficulty breathing after using Asmol inhaler.

In a few people, Asmol may cause a fall in potassium levels in a few people. Your doctor may do blood tests to check this.

Other side effects not listed above may also occur in some patients. Tell your doctor if you notice anything that is making you feel unwell.

After using Asmol inhaler

Straight after use, replace the mouthpiece cover firmly and click it into position.

Cleaning

Regular cleaning is required.

It is recommended that you clean your Asmol inhaler once a week.

Follow these steps to clean your inhaler:

Remove the metal can from the plastic holder of your inhaler and remove the mouthpiece cover.

Rinse the plastic holder and mouthpiece cover under warm running water.

Dry the plastic holder and mouthpiece cover thoroughly inside and out.

Put the can back into the plastic holder and replace the mouthpiece cover.

Do not put the metal can in water.

If you use a spacer device, clean it once each month. Wash the spacer in warm water and detergent then rinse clean with water. Allow it to air dry; do not use a cloth to dry it.

Storage

Keep Asmol inhaler where children cannot reach it. A locked cupboard at least one-and-a-half metres above the ground is a good place to store medicines.

Keep Asmol inhaler in a cool dry place where the temperature stays below 30°C.

Do not store Asmol inhaler or any other medicine in the bathroom or near a sink.

Do not leave Asmol inhaler in the car or on window sills. Heat and dampness can destroy some medicines.

Disposal

If your doctor tells you to stop using Asmol inhaler, or your medicine has passed its expiry date, ask your pharmacist what to do with the inhaler.

Do not burn or puncture the metal can, even when it is empty. The metal can is pressurised and may explode when punctured or burned.

You can recycle the plastic holder and the mouthpiece cover of your inhaler with other plastic things.

If you have any other questions, ask your doctor or pharmacist.

Product description

What it looks like

Asmol inhaler consists of a metal can inside a blue plastic holder with a dark blue mouthpiece cover.

Each Asmol inhaler contains 200 puffs.

Ingredients

The active ingredient in Asmol inhaler is salbutamol (sulfate). Each puff contains 100 micrograms of salbutamol.

Asmol inhaler also contains HFA-134a as the propellant. Asmol inhaler has no other additives.

Asmol inhaler is CFC-free.

Supplier

Asmol inhaler is supplied by: Alphapharm Pty Limited (ABN 93 002 359 739) Level 1, 30 The Bond 30 - 34 Hickson Road Millers Point NSW 2000 Phone: (02) 9298 3999 www. alphapharm. com. au

Australian Registration Number: Asmol CFC free inhaler - Aust R 65639

This leaflet was prepared on 7 October 2014.

Published by MIMS January 2015

Consumers should be aware that the information provided by the Consumer Medicines Information (CMI) search (CMI Search) is for information purposes only and consumers should continue to obtain professional advice from a qualified healthcare professional regarding any condition for which they have searched for CMI. CMIs are provided by MIMS Australia. CMI is supplied by the relevant pharmaceutical company for each consumer medical product. All copyright and responsibility for CMI is that of the relevant pharmaceutical company. MIMS Australia uses its best endeavours to ensure that at the time of publishing, as indicated on the publishing date for each resource (e. g. Published by MIMS/myDr January 2007), the CMI provided was complete to the best of MIMS Australia's knowledge. The CMI and the CMI Search are not intended to be used by consumers to diagnose, treat, cure or prevent any disease or for any therapeutic purpose. Cirrus Media Pty Limited, its servants and agents shall not be responsible for the continued currency of the CMI, or for any errors, omissions or inaccuracies in the CMI and/or the CMI Search whether arising from negligence or otherwise or from any other consequence arising there from.

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