Inverse tangent function, actan

Documentation

arctan

Description

arctan(x) represents the inverse of the tangent function.

arctan(y, x) is an alias for arg (x, y) .

The angle returned by this function is measured in radians, not in degrees. For example, the result π represents an angle of 180 o .

arctan is defined for complex arguments.

Floating-point values are returned for floating-point arguments. Floating-point intervals are returned for interval arguments. Unevaluated function calls are returned for most exact arguments.

If the argument is a rational multiple of I. the result is expressed in terms of hyperbolic functions. See Example 2 .

The inverse tangent function is multivalued. The MuPAD ® arctan function returns the value on the main branch. The branch cuts are the intervals ( − i ∞. − i ] and [ i.   i ∞ ) on the imaginary axis. Thus, arctan returns values, such that y = arctan ( x ) satisfies − π 2 < ℜ ( y ) < π 2 for any finite complex x .

The tan function returns explicit values for arguments that are certain rational multiples of π. For these values, arctan returns an appropriate rational multiple of π on the main branch. See Example 3 .

The values jump when the arguments cross a branch cut. See Example 4 .

The float attributes are kernel functions. Thus, floating-point evaluation is fast.

If you call arctan with two arguments, y and x. MuPAD calls the arg function that computes the polar angle of a complex number x + I*y. See Example 7 and the arg help page.

Environment Interactions

When called with a floating-point argument, arctan is sensitive to the environment variable DIGITS which determines the numerical working precision.

Select Your Country

Heating elements, gamatherm

Heating Elements

Gamma Therm Heaters manufactures heating elements for heating water, oil, air/gas, acids, lyes and solid bodies.

Gamma Therm Heaters has the know-how for customised production. Tailor-made solutions are developed quickly and at low price from the companyís own ideas or customer specifications, samples and drawings. Production of one-offs is daily practice at Gamma Therm.

Gamma Therm Heaters combines quality with technical perfection and is acclaimed as a reliable partner.

Gamma Therm Heaters consist of flexible, highly compact tubular heating elements or durable, exchangeable ceramic cartridges for fitting into all tubular casings. Casings are supplied in materials to suit the medium ñ in stainless steel, steel, copper, various other alloys and in high - corrosion proof materials.

Gamma Therm Heaters come equipped with or without caps, in various degrees of protection, with temperature controller, cutout and further special devices, as per requirement.

Buy choltran

Cholestyramine powder

Cholestyramine powder is used for:

Lowering blood cholesterol levels. It is used along with changes in diet. It is also used to relieve itching caused by partial biliary obstruction. It may also be used for other conditions as determined by your doctor.

Cholestyramine powder is a bile acid sequestrant. It works by increasing the removal of bile acids from the body. As the body loses bile acids, it replaces them by converting cholesterol from the blood to bile acids. This causes the blood level of cholesterol to decrease.

Do NOT use cholestyramine powder if:

you are allergic to any ingredient in cholestyramine powder

you have a complete blockage of your biliary tract, severe constipation (eg, impacted feces), or high blood chloride levels

if you are taking leflunomide or mycophenolate

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

Before using cholestyramine powder:

Some medical conditions may interact with cholestyramine powder. 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

if you have heart disease (eg, heart blood vessel problems); constipation; hemorrhoids; stomach or bowel blockage; gallbladder problems; blood, bleeding, or clotting problems; high blood triglyceride levels; poor absorption from the intestinal tract or other intestinal problems; kidney problems; or phenylketonuria (PKU)

if you have diabetes, underactive thyroid, or liver problems, or if you are addicted to alcohol

if you are dehydrated or have low blood volume

Some MEDICINES MAY INTERACT with cholestyramine powder. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), beta-blockers (eg, propranolol), deferasirox, digoxin, digitoxin, diuretics (eg, furosemide, hydrochlorothiazide), estrogens, hormonal contraceptives (eg, birth control pills), leflunomide, mycophenolate, penicillins (eg, amoxicillin), phenobarbital, phenylbutazone, phosphate supplements, progestins (eg, medroxyprogesterone), tetracyclines (eg, doxycycline), or thyroid hormones (eg, levothyroxine) because their effectiveness may be decreased by cholestyramine powder

Spironolactone because the risk of high blood chloride levels may be increased

This may not be a complete list of all interactions that may occur. Ask your health care provider if cholestyramine powder 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 cholestyramine powder:

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

Take cholestyramine powder by mouth at mealtime as directed, unless your doctor tells you otherwise.

Cholestyramine powder may decrease the absorption of other medicines. Take other medicines at least 1 hour before or 4 to 6 hours after you take cholestyramine powder. Check with your doctor if you have any questions about how to take your other medicines along with cholestyramine powder.

If you are also taking anticoagulants (eg, warfarin), diuretics (eg, furosemide, hydrochlorothiazide), or thyroid hormones (eg, levothyroxine), ask your doctor how you should take them with cholestyramine powder.

Do not take cholestyramine powder in its dry form. Always mix with water or other fluids before taking.

Add the prescribed amount of medicine to 2 to 6 ounces (60 to 180 mL) of water or other noncarbonated liquid. Stir until well mixed (it will not dissolve). After you drink cholestyramine powder, rinse the glass with more liquid and drink it to be sure that all medicine is taken.

Cholestyramine powder may also be mixed with soups (chicken noodle, tomato) or fruits (eg, applesauce, crushed pineapple) that contain plenty of fluid.

Do not sip cholestyramine powder or hold it in your mouth for a long period of time. This may cause tooth changes such as discoloration, decay, or erosion of enamel. Be sure to use good oral hygiene while you are using cholestyramine powder.

Drink several glasses (8 ounces [240 mL]) of water or other liquid daily, unless directed otherwise by your doctor.

If you miss a dose of cholestyramine powder, take 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 take 2 doses at once.

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

Important safety information:

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

If you experience constipation while taking cholestyramine powder, talk to your doctor about increased fiber intake and use of a stool softener to help relieve this side effect.

Phenylketonuria patients - Some of these products contain phenylalanine. If you must have a diet that is low in phenylalanine, ask your pharmacist if it is in your product.

The color of the powder may vary from batch to batch. This is normal and does not change the effect.

Hormonal birth control (eg, birth control pills) may not work as well while you are using cholestyramine powder. To prevent pregnancy, use an extra form of birth control (eg, condoms).

Lab tests, including triglyceride and cholesterol levels, may be performed while you use cholestyramine powder. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use cholestyramine powder with caution in the ELDERLY; they may be more sensitive to its effects, especially constipation.

Caution is advised when using cholestyramine powder in CHILDREN; they may be more sensitive to its effects, especially high blood chloride levels.

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using cholestyramine powder while you are pregnant. It is not known if this medicine is found in breast milk. If you are or will be breast-feeding while you use cholestyramine powder, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of cholestyramine powder:

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:

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); black or bloody stools; irritation of the skin, tongue, or anal area; severe or persistent constipation; severe or persistent nausea; shortness of breath; sluggishness; stomach pain; unusual bruising or bleeding; vomiting.

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. Symptoms may include constipation; feeling of fullness.

Proper storage of cholestyramine powder:

Store cholestyramine powder at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep cholestyramine powder out of the reach of children and away from pets.

General information:

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

Cholestyramine powder 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 cholestyramine powder 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 cholestyramine powder. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to cholestyramine powder. 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 cholestyramine powder.

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 cholestyramine

Blue Train

iTunes Review

John Coltrane’s only date as a leader for Blue Note has become both a popular favorite and a classic in the legendary saxophonist/composer/bandleader’s considerable discography. Recorded in 1957, Blue Train features four Coltrane originals, plus a lovely version of the standard “I’m Old Fashioned.” Trumpeter Lee Morgan, then 19 years old, is impressively able to keep up with the boss’s already-mythical flurry of notes and ideas, particularly on the opening title track. Bassist Paul Chambers and drummer Philly Joe Jones played with Coltrane in Miles Davis’ band, and pianist Kenny Drew rounds out the rhythm section. "Moment’s Notice” is Coltrane’s most enduring composition from this date, while “Locomotion” has spirited solos by both Jones and trombonist Curtis Fuller.

Customer Reviews

Flawless music in a flawless format

I couldn't be happier to get this legendary album in Mastered for iTunes format. This will instantly become one of my test tracks I use setting up the HiFi systems I design.

Amazing

One of his best albums to date along with Giant Steps

Biography

Born: September 23, 1926 in Hamlet, NC

Years Active: '40s, '50s, '60s

Despite a relatively brief career (he first came to notice as a sideman at age 29 in 1955, formally launched a solo career at 33 in 1960, and was dead at 40 in 1967), saxophonist John Coltrane was among the most important, and most controversial, figures in jazz. It seems amazing that his period of greatest activity was so short, not only because he recorded prolifically, but also because, taking advantage of his fame, the record companies that recorded him as a sideman in the 1950s frequently reissued.

Top Albums and Songs by John Coltrane

Listeners Also Bought

View in iTunes

$5.99

Genres: Jazz. Music. Blues. Hard Bop

Released: Sep 15, 1957

? 2012 Blue Note Records. All rights reserved. Unauthorized reproduction is a violation of applicable laws. Manufactured by Blue Note Records, 150 Fifth Avenue, New York, NY 10011.

Customer Ratings

Influencers

Influenced by This Artist

Contemporaries

Discover and share new apps.

Discover and share new music, movies, TV, books, and more.

Follow us @iTunes and discover new iTunes Radio Stations and the music we love.

Giant Steps Original recording remastered, Extra tracks

The Autorip free MP3 program is not applicable to gift orders.

AutoRip Terms & Conditions

Last updated January 12, 2016

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AutoRip is available only to customers with billing addresses in the United States who have a U. S. bank-issued credit card associated with their Amazon. com account.

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Description

About this item

The Very Best of John Coltrane

Album Review

This isn't the first CD that has had the title The Very Best of John Coltrane, and one can safely assume that it won't be the last. The focus of this 74-minute collection is Coltrane's Impulse output — specifically, modal post-bop that he recorded from 1961-1964. The disc doesn't get into the blistering atonal free jazz he embraced from 1965-1967, which is just as well because even though much of that material is brilliant, it isn't for everyone — at least not novices and casual listeners who are exploring the saxophonist's work for the first time. And for those who need a dose of introductory Coltrane, this release generally favors the more essential recordings that he provided for Impulse. That includes "Acknowledgement," "Bessie's Blues," and "Crescent," as well as legendary encounters with Duke Ellington ("In a Sentimental Mood") and singer Johnny Hartman ("Lush Life"). Because Impulse didn't have access to Coltrane's famous Atlantic recordings of "My Favorite Things" and "Naima," they chose live versions from various Impulse releases — both of which are excellent, but not essential. This CD would have been better off with "After the Rain," "Miles' Mode," or "India," none of which are included. Also questionable is Impulse's decision to include a previously unreleased 1962 studio performance of "Impressions," which should have been saved for a collection of rarities — this is supposed to be a best-of, after all. But all things considered, The Very Best of John Coltrane can serve as a rewarding introduction to the saxman's Impulse period. While this 2001 release is hardly the last word on Coltrane's legacy, it is one of the CDs to start out with for novices.

Customer Reviews

Coltrane 101

by Jv On The Run

don't know where to start? buy this album and then buy "Love Supreme", John Coltrane/Johnny Hartman", "Ballads", "Crescent".

Amazing!

This is one amazing jazz album. There is always something about jazz that really makes you just want to go relax. If you want a great album and some amazing music to listen to this is the one, you can never go wrong with this genre, there is so many talented artists in jazz and so many different styles, this is just one style, but one great example. Support the artists that deserve the money, help them to keep going, and keep coming out with new albums, and always support the greats.

For the drifting soul

His music is rich with human emotion, improvisation, and essence of the soul. Money well spent.

Biography

Born: September 23, 1926 in Hamlet, NC

Years Active: '40s, '50s, '60s

Despite a relatively brief career (he first came to notice as a sideman at age 29 in 1955, formally launched a solo career at 33 in 1960, and was dead at 40 in 1967), saxophonist John Coltrane was among the most important, and most controversial, figures in jazz. It seems amazing that his period of greatest activity was so short, not only because he recorded prolifically, but also because, taking advantage of his fame, the record companies that recorded him as a sideman in the 1950s frequently reissued.

Top Albums and Songs by John Coltrane

Bicalutamide oral uses, side effects, interactions, pictures, warnings - dosing, bikalutamid

bicalutamide

Uses

Bicalutamide is used to treat prostate cancer that has spread to other areas of the body. It is used in combination with hormone treatment. This medication works by blocking the action of male hormones in the prostate. slowing growth of the tumors.

This medication should not be used in women or children.

How to use bicalutamide

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

Take this medication by mouth with or without food as directed by your doctor, usually once a day (either in the morning or in the evening).

Use this medication regularly in order to get the most benefit from it. Remember to use it at the same time each day.

Do not increase your dose or take this medication more often without your doctor's approval. Your condition will not improve any faster, and the risk of serious side effects may be increased.

Since this drug can be absorbed through the skin. women who are pregnant or who may become pregnant should not handle this medication.

Side Effects

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: decreased sexual ability/desire, vision changes, numbness/tingling of the hands or feet, swelling of the arms/legs, unusual or easy bleeding/bruising, change in the amount of urine, painful urination. signs of infection (e. g. fever, chills, persistent sore throat ), trouble breathing. persistent cough. mental/mood changes (e. g. anxiety. depression ).

Get medical help right away if you have any very serious side effects, including: chest/jaw/left arm pain.

Rarely, bicalutamide may cause growth of other types of tumors. Consult your doctor right away if new lumps or growths occur.

This medication may rarely cause serious (possibly fatal) liver disease. Get medical help right away if any of these side effects occur: dark urine, yellowing of the eyes /skin, unusual tiredness, severe stomach /abdominal pain. persistent nausea/vomiting.

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 bicalutamide, 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: liver disease, diabetes. lung /breathing problems.

This drug may make you dizzy or drowsy. Do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely. To minimize these effects and flushing of the face, limit alcoholic beverages.

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.

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

Bicalutamide should not be used in women or children. It must not be used in a woman who may be pregnant or breast - feeding. This medication may cause harm to an unborn or breast-feeding baby .

Interactions

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.

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.

Notes

Do not share this medication with others.

Laboratory and/or medical tests (e. g. prostate specific antigen-PSA levels. liver and kidney function tests, blood sugar. complete blood counts) should be performed to monitor your progress or check for side effects. Consult your doctor for more details.

Missed Dose

If you miss a 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

Selected from data included with permission and copyrighted by First Databank, Inc. This copyrighted material has been downloaded from a licensed data provider and is not for distribution, expect as may be authorized by the applicable terms of use.

CONDITIONS OF USE: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for you or anyone else. A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.

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ADHD Drug Side Effects

Drug Overdose

Glimide - antiarrhythmic agents, hypoglycemic agents, sulfonylureas, atc a10bb, glimide

Glimide

Tablet (1.25 mg, 2.5 mg, 5 mg)

Glimide Indication

Indicated as an adjunct to diet to lower the blood glucose in patients with non-insulin-dependent diabetes mellitus (Type II) whose hyperglycemia cannot be satisfactorily controlled by diet alone.

Glimide Pharmacology

Glyburide, a second-generation sulfonylurea antidiabetic agent, appears to lower the blood glucose acutely by stimulating the release of insulin from the pancreas, an effect dependent upon functioning beta cells in the pancreatic islets. With chronic administration in Type II diabetic patients, the blood glucose lowering effect persists despite a gradual decline in the insulin secretory response to the drug. Extrapancreatic effects may be involved in the mechanism of action of oral sulfonyl-urea hypoglycemic drugs. The combination of glyburide and metformin may have a synergistic effect, since both agents act to improve glucose tolerance by different but complementary mechanisms. In addition to its blood glucose lowering actions, glyburide produces a mild diuresis by enhancement of renal free water clearance. Glyburide is twice as potent as the related second-generation agent glipizide.

Glimide Absorption

Significant absorption within 1 hour and peak plasma levels are reached within 4 hours.

Glimide side effects and Toxicity

Oral rat LD 50 . > 20,000 mg/kg. Oral mouse LD 50 . 3250 mg/kg.

Glimide Patient Information

Patients should be informed of the potential risks and advantages of MICRONASE and of alternative modes of therapy. They also should be informed about the importance of adherence to dietary instructions, of a regular exercise program, and of regular testing of urine and/or blood glucose.

The risks of hypoglycemia, its symptoms and treatment, and conditions that predispose to its development should be explained to patients and responsible family members. Primary and secondary failure also should be explained.

Glimide Organisms Affected

Humans and other mammals

Betamethasone - brand name list from, camnovate

Betamethasone

See also.

Disclaimer: The indications, uses and warnings for individual medications outside the USA are determined by local regulatory bodies in each country or region. The Drugs. com website is intended primarily for audiences in the United States and its territories. Indications, uses and warnings on Drugs. com patient information leaflets are derived from FDA product labels and may differ in countries outside the USA. Every effort has been made to ensure that the information provided on this page is accurate, up-to-date and complete, but no guarantee is made to that effect. Drugs. com does not endorse drugs, diagnose patients or recommend specific therapies. The information on this page is not a substitute for the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that a drug or drug combination is safe, effective or appropriate for any given patient. Drugs. com does not assume any responsibility for any aspect of healthcare administered with the aid of information provided here. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. Always consult your doctor or healthcare specialist for medical advice.

Chemical formula: C22H29FO5 Drugbank ID: DB00443 ATC code(s): A07EA04, C05AA05, D07AC01, D07BC01, D07CC01, D07XC01, H02AB01, R01AD06, R03BA04, S01BA06, S01BB04, S01CA05, S01CB04, S02BA07, S03BA03, S03CA06

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Glevo 500mg; tablet, glenmark pharmaceuticals limited, glevo 500mg

GLEVO 500mg - Tablet, Glenmark Pharmaceuticals Limited

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If you are pharmaceutical retailer or chemist then this place for you to increase your sales and get medicine enquiry from common person. You can find pharmaceutical dealers and stockiest list according to your city for any pharmaceutical company and its product.

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Dawabazar. in is a free content encyclopedia especially for pharmaceutical field. This website provides information about all manufacturing. marketing companies and their products, its compositions along with its dealers. retailers in India. This website also provides many findings on medicines, Pharma companies, Pharma dealers, Pharma retailers, active pharmaceutical ingredients, therapeutic index and pharmacological index which is useful for doctors. medical students and common person.

Ketorolac medical facts from, ketorolaco

ketorolac

What is ketorolac?

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

Ketorolac is used short-term (5 days or less) to treat moderate to severe pain.

Ketorolac may also be used for other purposes not listed in this medication guide.

What is the most important information I should know about ketorolac?

This medicine can increase your risk of life-threatening heart or circulation problems, including heart attack or stroke. This risk will increase the longer you use ketorolac. Do not use this medicine just before or after having heart bypass surgery (also called coronary artery bypass graft, or CABG).

Seek emergency medical help if you have symptoms of heart or circulation problems, such as chest pain, weakness, shortness of breath, slurred speech, or problems with vision or balance.

This medicine can also increase your risk of serious effects on the stomach or intestines, including bleeding or perforation (forming of a hole). These conditions can be fatal and gastrointestinal effects can occur without warning at any time while you are taking ketorolac. Older adults may have an even greater risk of these serious gastrointestinal side effects.

Call your doctor at once if you have symptoms of bleeding in your stomach or intestines. This includes black, bloody, or tarry stools, or coughing up blood or vomit that looks like coffee grounds.

Do not drink alcohol while taking ketorolac. Alcohol can increase the risk of stomach bleeding caused by ketorolac.

What should I discuss with my healthcare provider before taking ketorolac?

Do not use this medication if you are allergic to ketorolac, aspirin, or other NSAIDs, or if you have:

severe kidney disease;

a bleeding or blood clotting disorder;

a closed head injury or bleeding in your brain;

a stomach ulcer or a history of stomach or intestinal bleeding; or

if you are breast-feeding a baby.

Do not take ketorolac if you are also taking pentoxifylline (Trental) or probenecid (Benemid). Do not take ketorolac with aspirin or other NSAIDs such as ibuprofen (Motrin, Advil), naproxen (Aleve, Naprosyn), diclofenac (Voltaren), diflunisal (Dolobid), etodolac (Lodine), flurbiprofen (Ansaid), indomethacin (Indocin), ketoprofen (Orudis), ketorolac (Toradol), mefenamic acid (Ponstel), meloxicam (Mobic), nabumetone (Relafen), or piroxicam (Feldene).

Taking an NSAID can increase your risk of life-threatening heart or circulation problems, including heart attack or stroke. This risk will increase the longer you use an NSAID. Do not use this medicine just before or after having heart bypass surgery (also called coronary artery bypass graft, or CABG).

NSAIDs can also increase your risk of serious effects on the stomach or intestines, including bleeding or perforation (forming of a hole). These conditions can be fatal and gastrointestinal effects can occur without warning at any time while you are taking an NSAID. Older adults may have an even greater risk of these serious gastrointestinal side effects.

Before taking ketorolac, tell your doctor if you are allergic to any drugs, or if you have:

a history of heart attack, stroke, or blood clot;

heart disease, congestive heart failure, high blood pressure;

liver or kidney disease,

ulcerative colitis or Crohn's disease;

polyps in your nose;

if you have recently had surgery; or

If you have any of these conditions, you may need a dose adjustment or special tests to safely take ketorolac.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Taking ketorolac during labor can increase the risk of bleeding during childbirth. Do not take ketorolac during pregnancy unless your doctor has told you to.

This medication can affect fertility (your ability to have children). Do not take ketorolac while you are trying to get pregnant.

Ketorolac can pass into breast milk and may harm a nursing baby. Do not take this medicine without telling your doctor if you are breast-feeding a baby.

Do not give this medicine to anyone younger than 18 years old.

How should I take ketorolac?

Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label. Ketorolac is not for treating minor aches and pains.

Ketorolac is usually given first as an injection, and then as an oral (by mouth) medicine. Ketorolac injection is given through a needle into a muscle or a vein. Your doctor, nurse, or other healthcare provider will give you this injection.

The ketorolac tablet should be taken with a full glass of water.

Ketorolac is normally given for 5 days or less, including both the injection and oral forms combined. Long-term use of ketorolac can damage your kidneys or cause bleeding.

If you need to have any type of surgery, tell the surgeon ahead of time if you have recently used ketorolac.

Store ketorolac tablets at room temperature away from moisture and heat.

What happens if I miss a dose?

Since ketorolac is taken as needed for pain, you may not be on a dosing schedule. And if you receive ketorolac injection in a hospital setting, it is not likely that you will miss a dose.

If you are taking the medication regularly, 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 regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include nausea, vomiting, stomach pain, drowsiness, black or bloody stools, coughing up blood, urinating less than usual, shallow breathing, and fainting.

What should I avoid while taking ketorolac?

Do not use any other over-the-counter cold, allergy, or pain medication without first asking your doctor or pharmacist. Many medicines available over the counter contain aspirin or other medicines similar to ketorolac (such as ibuprofen, ketoprofen, or naproxen). If you take certain products together you may accidentally take too much of this type of medication. Read the label of any other medicine you are using to see if it contains aspirin, ibuprofen, ketoprofen, or naproxen.

Do not drink alcohol while taking ketorolac. Alcohol can increase the risk of stomach bleeding caused by ketorolac.

Ketorolac side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Stop taking ketorolac and seek medical attention or call your doctor at once if you have any of these serious side effects:

chest pain, weakness, shortness of breath, slurred speech, problems with vision or balance;

black, bloody, or tarry stools;

coughing up blood or vomit that looks like coffee grounds;

swelling or rapid weight gain;

urinating less than usual or not at all;

nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

fever, sore throat, and headache with a severe blistering, peeling, and red skin rash;

the first sign of any mouth sores or skin rash, no matter how mild;

pale skin, easy bruising, severe tingling, numbness, pain, muscle weakness; or

fever, headache, neck stiffness, chills, increased sensitivity to light, purple spots on the skin, and/or seizure (convulsions).

Less serious side effects may include:

upset stomach, mild nausea or vomiting, diarrhea, constipation;

mild heartburn, stomach pain, bloating, gas;

dizziness, headache, drowsiness;

ringing in your ears.

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.

Ketorolac dosing information

Usual Adult Dose for Pain:

The combined duration of use of parenteral, oral, and intranasal ketorolac should not exceed 5 days; the oral formulation is only to be used as continuation to IV or IM therapy.

Intranasal: - Weight 50 kg or more: 31.5 mg every 6 to 8 hours (1 spray in each nostril) - Weight less than 50 kg: 15.75 mg every 6 to 8 hours (1 spray in 1 nostril) - Maximum dose: 4 doses per day

Parenteral: Single-Dose Treatment: - Weight 50 kg or more: 60 mg IM or 30 mg IV - Weight less than 50 kg: 30 mg IM or 15 mg IV Multiple-Dose Treatment: - Weight 50 kg or more: 30 mg IM/IV every 6 hours as needed Maximum dose: 120 mg/day - Weight less than 50 kg: 15 mg IM/IV every 6 hours as needed Maximum dose: 60 mg/day

Oral, as continuation to parenteral therapy: Weight 50 kg or more: 20 mg orally once followed by 10 mg every 4 to 6 hours as needed Weight less than 50 kg: 10 mg orally once followed by 10 mg every 4 to 6 hours as needed Maximum dose: 40 mg/day

Comments: - Do not increase the dose or frequency for breakthrough pain; consider supplementing with low dose opioids as needed, if appropriate. - Use minimum effective dose, and switch to alternative analgesics as soon as possible

Use: For the short-term (5 days or less) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting.

Usual Geriatric Dose for Pain:

The combined duration of use of parenteral, oral, and intranasal ketorolac should not exceed 5 days; the oral formulation is only to be used as continuation to IV or IM therapy.

Intranasal: - Dose: 15.75 mg every 6 to 8 hours (one spray in 1 nostril) - Maximum dose: 4 doses per day

Parenteral: - Single-Dose Treatment: 30 mg IM or 15 mg IV - Multiple-Dose Treatment: 15 mg IM/IV every 6 hours as needed Maximum dose: 60 mg/day

Oral, as continuation to parenteral therapy: - Dose: 10 mg orally once followed by 10 mg every 4 to 6 hours as needed Maximum dose: 40 mg/day

Comments: - Do not increase the dose or frequency for breakthrough pain; consider supplementing with low dose opioids as needed, if appropriate. - Use minimum effective dose and switch to alternative analgesics as soon as possible

Use: For the short-term (5 days or less) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting.

Usual Pediatric Dose for Pain:

The combined duration of use of parenteral, oral, and intranasal ketorolac should not exceed 5 days; the oral formulation is only to be used as continuation therapy to IV or IM.

Intranasal: Age: Greater than 17 years: - Weight 50 kg or more: 31.5 mg every 6 to 8 hours (1 spray in each nostril) - Weight less than 50 kg: 15.75 mg every 6 to 8 hours (1 spray in 1 nostril) - Maximum: 4 doses per day

Oral, as continuation to parenteral therapy: Age: 17 years or older: - Weight 50 kg or more: 20 mg orally once followed by 10 mg every 4 to 6 hours as needed - Weight less than 50 kg: 10 mg orally once followed by 10 mg every 4 to 6 hours as needed Maximum dose: 40 mg/day

Parenteral: Age: 17 years or older: Single-Dose Treatment: - Weight 50 kg or more: 60 mg IM or 30 mg IV - Weight less than 50 kg: 30 mg IM or 15 mg IV Multiple-Dose Treatment: - Weight 50 kg or more: 30 mg IM/IV every 6 hours as needed Maximum dose: 120 mg/day - Weight less than 50 kg: 15 mg IM/IV every 6 hours as needed Maximum dose: 60 mg/day

Age: 2 to 16 years: Single-Dose Treatment: IM: 1 mg/kg up to a maximum of 30 mg IV: 0.5 mg/kg up to a maximum of 15 mg Maximum dose: 1 dose

Comments: - Do not increase the dose or frequency for breakthrough pain; consider supplementing with low dose opioids as needed, if appropriate. - Use minimum effective dose and switch to alternative analgesics as soon as possible

Use: For the short-term (5 days or less) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting.

What other drugs will affect ketorolac?

Tell your doctor if you are taking an antidepressant such as citalopram (Celexa), duloxetine (Cymbalta), escitalopram (Lexapro), fluoxetine (Prozac, Sarafem, Symbyax), fluvoxamine (Luvox), paroxetine (Paxil), sertraline (Zoloft), or venlafaxine (Effexor). Taking any of these drugs with ketorolac may cause you to bruise or bleed easily.

Before taking ketorolac, tell your doctor if you are taking any of the following drugs:

a blood thinner such as warfarin (Coumadin);

lithium (Eskalith, Lithobid);

methotrexate (Rheumatrex, Trexall);

Agn stock price & news - allergan plc - wall street journal, alergan

Allergan PLC AGN (U. S. NYSE)

P/E Ratio (TTM) The Price to Earnings (P/E) ratio, a key valuation measure, is calculated by dividing the stock's most recent closing price by the sum of the diluted earnings per share from continuing operations for the trailing 12 month period. Earnings Per Share (TTM) A company's net income for the trailing twelve month period expressed as a dollar amount per fully diluted shares outstanding. Market Capitalization Reflects the total market value of a company. Market Cap is calculated by multiplying the number of shares outstanding by the stock's price. For companies with multiple common share classes, market capitalization includes both classes. Shares Outstanding Number of shares that are currently held by investors, including restricted shares owned by the company's officers and insiders as well as those held by the public. Public Float The number of shares in the hands of public investors and available to trade. To calculate, start with total shares outstanding and subtract the number of restricted shares. Restricted stock typically is that issued to company insiders with limits on when it may be traded. Dividend Yield A company's dividend expressed as a percentage of its current stock price.

Key Stock Data

P/E Ratio (TTM)

EPS (TTM)

Market Cap

Shares Outstanding

Public Float

Yield

AGN has not issued dividends in more than 1 year.

Latest Dividend

Ex-Dividend Date

Shares Sold Short The total number of shares of a security that have been sold short and not yet repurchased. Change from Last Percentage change in short interest from the previous report to the most recent report. Exchanges report short interest twice a month. Percent of Float Total short positions relative to the number of shares available to trade.

Short Interest (08/31/16)

Shares Sold Short

Change from Last

Percent of Float

Money Flow Uptick/Downtick Ratio Money flow measures the relative buying and selling pressure on a stock, based on the value of trades made on an "uptick" in price and the value of trades made on a "downtick" in price. The up/down ratio is calculated by dividing the value of uptick trades by the value of downtick trades. Net money flow is the value of uptick trades minus the value of downtick trades. Our calculations are based on comprehensive, delayed quotes.

Stock Money Flow

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Glevo tablets (levofloxacin), glevo 750mg

Life Pharmaceutical Company

Life Pharmaceutical Company

Glevo Tablets (Levofloxacin) by Life Pharmaceutical Company

Drug Category: Quinolones/ Antibiotics, systemic

Indication: Levofloxacin is primarily indicated in conditions like Bronchiolitis, Bronchitis, Complicated UTIS, Folliculitis, Nephrogenic and partial pituitary diabetes insipidus, Oedema, Otitis externa, Pneumonia, Pyelonephritis, Respiratory tract infections, Short-term treatment of severe congestive heart failure, Skin and soft tissue infections.

Levofloxacin: Levofloxacin inhibits bacterial type II topoisomerases, topoisomerase IV and DNA gyrase. Levofloxacin, like other fluoroquinolones, inhibits the A subunits of DNA gyrase, two subunits encoded by the gyrA gene. This results in strand breakage on a bacterial chromosome, supercoiling, and resealing; DNA replication and transcription is inhibited.

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Arcoxia 60mg tablets, arcoxia

ARCOXIA 60MG TABLETS

Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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Drugs. com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Data sources include Micromedex® (updated Sep 2nd, 2016), Cerner Multum™ (updated Sep 5th, 2016), Wolters Kluwer™ (updated Aug 8th, 2016) and others. To view content sources and attributions, please refer to our editorial policy .

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ARCOXIA 60MG TABLETS

Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

FDA Consumer Updates

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Drugs. com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Data sources include Micromedex® (updated Sep 2nd, 2016), Cerner Multum™ (updated Sep 5th, 2016), Wolters Kluwer™ (updated Aug 8th, 2016) and others. To view content sources and attributions, please refer to our editorial policy .

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Buy skincare - diamalin (brand name retin-a 0, 025) online - order tretinoin - purchase skincare - d

Retin-A is often used to improve the appearance and texture of the skin. It produces a mild, superficial peel of the epidermis. Retin-A has effects on the both the superficial (epidermis) and the deep (dermis) parts of the skin. The major benefit is to decrease the effects of sunlight caused aging by increasing the speed with which the surface cells are replaced.

Apply a thin layer to affected area once a day at bedtime. Use a gauze pad or cotton swab to apply the liquid. Wash your hands immediately after use. Using this medication more frequently or in excessive amounts does not improve the results, but may increase side effects. Avoid applying near the eyes, mouth, or open cuts since this medication can irritate sensitive skin. Acne may appear to worsen when the medication is first used; continue therapy. It may take three to six weeks before the full benefits of this medication are seen. Use mild soap when washing your face. Do not wash face excessively. Abrasive soaps, cleansers, medicated creams or lotions can increase skin irritation. Consult your doctor or pharmacist about their use. Use other acne preparations with caution while using this medication. Drug Class and Mechanism

Tretinoin is a derivative of vitamin A. Topical Tretinoin is used in the treatment of mild to moderate acne and on skin that has been damaged by excessive exposure to the sun. Tretinoin irritates the skin and causes the cells of the skin to grow (divide) and die more rapidly, that is, it increases the turnover of cells. The number of layers of cells in the skin actually is reduced. In patients with acne, new cells replace the cells of existing pimples, and the rapid turnover of cells prevents new pimples from forming. By a similar mechanism, Tretinoin can reduce some wrinkles, areas of darkened skin, and rough areas of skin, all of which occur in sun-damaged skin. In patients with sun-damaged skin, improvements in the skin usually are seen within the first 3 to 4 weeks of treatment. Brown spots begin to fade after six to eight weeks. Wrinkles decrease or disappear after three to six months. Following application to the skin, a minimal amount of drug is absorbed into the body.

If you miss a dose, use it as soon as remembered; do not use if it is almost time for the next dose, skip the missed dose and resume your usual dosing schedule. Do not "double-up" the dose to catch up.

Store at room temperature away from sunlight. Keep this and all medications out of the reach of children.

This medication can increase sensitivity to sunlight, wind and cold. Avoid prolonged exposure to the sun and sunlamps. Wear protective clothing and use an effective sunscreen. This medication should be used during pregnancy only if clearly needed. It is not known if Retin-A appears in breast milk. Consult your doctor before breast-feeding.

Possible Side Effects

Due to the possibility of irritation, it is advisable to begin treatment on a small area of skin. Exposure to the sun or to ultraviolet rays causes additional irritation. During treatment, such exposure should be avoided as much as possible or a sun block should be used. During the first weeks of treatment there may be an apparent worsening of the problem. Such a reaction is perfectly normal because small cysts deep within the skin are being eliminated at an accelerated rate. This medication can increase sensitivity wind and cold. Avoid prolonged exposure to the sun and sunlamps. Wear protective clothing and use an effective sunscreen. If any ingredient should cause hypersensitivity, discontinue use.

Serious side effects are not likely to occur. Stop using tretinoin topical and seek emergency medical attention if you experience an allergic reaction (shortness of breath; closing of your throat; swelling of your lips, face, or tongue; or hives). You may experience some burning, warmth, stinging, tingling, itching, redness, swelling, dryness, peeling, or irritation while you are using tretinoin topical. If these side effects are excessive, talk to your doctor. You may need a lower dose or less frequent applications of tretinoin topical. If you notice a change in your skin color, contact your doctor. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

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Diclofenac

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History - riyadh pharma, riyad pharma

History

Medical And Cosmetic Products Company Limited, Riyadh Pharma Established to be a building block of the pharmaceutical industry in the Kingdom of Saudi Arabia, according to the latest standards, scientific and industrial technologies, for the production and marketing of many drugs of high quality both inside and outside the Kingdom of Saudi Arabia and medical disinfectants. Riyadh Pharma occupies a leading position in the pharmaceutical industry in the Saudi market, enabling it to maintain a significant growth rate, reflected in the strong and vital presence in foreign markets.

Riyadh Pharma considered as one of the most successful companies in the manufacturing and supply of health care products in Saudi Arabia, through the provision of a wide range of high quality and specialized services products introduced a wide range of medicines under license for companies European and American global medicines covering a wide range of diseases and meet the needs of customers. The share is performed as an example, and the focus of attention and respect of many local and international companies.

Riyadh Pharma plant granted Good Manufacturing Practice license (GMP) in 1998, and was registered in the Kingdom of Saudi Arabia, it was also registered the factory and products in a number of other Arab countries, and there is a plan for the registration of the company’s products in Europe and the United States of America Riyadh Pharma factory consists of four floors with an area of 22 thousand square meters and the building is located on an area of 15 thousand square meters in the heart of Riyadh in the third Industrial Zone.

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Lamisil - anti fungal, terbinax

Product Description Common use Lamisil is an anti-fungal antibiotic used to treat tinea versicolor, a fungal infection that produces brown, tan, white spots on the trunk of the body or other fungal infections such as athlete's foot, jock itch, and ringworm. Lamisil works by killing sensitive fungi by interfering with the formation of the fungal cell membrane.

Dosage and direction Take it orally with full glass of water. Swallow it without chewing. Usually it taken for 6 to 12 weeks. The recommended dose is different from type of infection: 1. For onychomycosis: Adults and teenagers 250 mg once a day for 6 to 12 weeks. Lamisil is used in children just after doctor's permission. 2. For tinea corporis: Adults and teenagers 250 mg once a day for 2 to 4 weeks. Lamisil is used in children just after doctor's permission. 3. For tinea cruris (ringworm of the groin; jock itch): Adults and teenagers 250 mg once a day for 2 to 4 weeks. Lamisil is used in children just after doctor's permission. 4. For tinea pedis: Adults and teenagers 250 mg once a day for 2 to 6 weeks. Lamisil is used in children just after doctor's permission. Note: this instruction presented here just for review. It's very necessary to consult your doctor before using.

Precautions Before using this medicine, consult your doctor or pharmacist if you have a certain blood disorder or severe liver disease. Don't forget to tell your medical history, especially if it includes lupus. Driving is not recommended while you are taking this medication because it may cause dizziness or less alertness. Drinking alcohol during treatment may cause a fast heartbeat and flushing of the skin. Avoid sun, tanning booths, and sunlamps and use a sunscreen and wear protective clothing when going outdoors. Lamisil should not be used during pregnancy, becoming pregnant or lactating without doctor's advice. Do not use before breast-feeding without doctor's advice.

Contraindications Lamisil is not allowed to people who have problems with their liver or kidneys, hypersensitive to any component of this dug.

Possible side effect They may include an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Also the most possible side effects include: joint pain or swelling, swollen glands, patchy skin color, or a butterfly-shaped skin rash over your cheeks and nose fever, chills, body aches, flu symptoms; changes in your vision; weight loss due to taste changes; scaly, itchy, and flaky skin rash; fever, sore throat, and headache with a severe blistering, peeling, and red skin rash. Less serious include: stomach pain, heartburn, diarrhea; headache; tired feeling; runny or stuffy nose, sore throat, cold symptoms; mild skin rash or itching; unusual or unpleasant taste in your mouth; or decreased taste sensation. If you experience one of them stop using Lamisil and tell your doctor as soon as possible. Also consult your doctor about any side effect that seems unusual.

Drug interaction Lamisil interacts with the following medications: Cyclosporine Metoprolol Nortriptyline Warfarin Also note that interaction between two medications does not always mean that you must stop taking one of them. As usual it affects the effect of drugs, so consult your doctor about its interactions.

Missed dose If you forgot to take your dose in time, please do it as soon as you remember. But do not take if it is too late or almost time for your next dose. Do not take double or extra doses. Take your usual dose next day at the same time regularly.

Overdose Symptoms of Lamisil overdose may include: dizziness, stomach pain, nausea, vomiting, skin rash, or urinating more than usual. If you experience one of them call your doctor immediately.

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 date.

Disclaimer We provide only general information about medications that does not cover all directions, possible drug integrations, or precautions. Information at 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.

Deep relief pain relief gel, dip rilif

DEEP RELIEF PAIN RELIEF GEL

Transcript

Patient Information Leaflet

Ibuprofen + Levomenthol Read all of this leaflet carefully before you start using this medicine. Read all of this lea?et carefully because it contains important information for you. This medicine is available without prescription. However, you still need to use Deep Relief Pain Relief Gel carefully to get the best results from it. • Keep this lea?et. You may need to read it again. • Ask your pharmacist if you need more information or advice. • You must see a doctor if your symptoms do not improve after 2 weeks. • If any of the side e?ects gets severe or you notice any side e?ects not listed in this lea?et please tell your doctor or pharmacist.

In this lea?et: 1. What Deep Relief Pain Relief Gel is and what it is used for 2. Before you use Deep Relief Pain Relief Gel 3. How to use Deep Relief Pain Relief Gel 4. Possible side e?ects 5. How to store Deep Relief Pain Relief Gel 6. Further information 1. What Deep Relief Pain Relief Gel is and what it is used for Deep Relief Pain Relief Gel is a pain relieving gel to be applied to the skin. It is used for the relief of: • Rheumatic pain (in muscles, tendons, joints or bones) • Muscular aches and pains • Pains and swellings such as strains, sprains and sports injuries. Deep Relief Pain Relief Gel contains two active ingredients. • Ibuprofen is one of a group of medicines called non-steroidal anti-in?ammatory drugs (NSAIDs) which provide e?ective pain relief and reduce both in?ammation and swelling. • Levomenthol provides a soothing sensation to calm the pain. 2. Before you use Deep Relief Pain Relief Gel Do not use Deep Relief Pain Relief Gel if you: • have an allergy to ibuprofen, menthol, or any of the ingredients in Deep Relief Pain Relief Gel (see end of Section 2 and Section 6) • have an allergy to aspirin or other pain-relieving medicines known as non-steroidal anti-in?ammatory drugs (NSAIDs) including those you take orally by mouth

• have asthma and know that aspirin or NSAIDs may bring on an asthma attack, a runny nose (rhinitis), itching or rashes • are more than 6 months pregnant • are breast feeding • have broken skin or your skin is infected or in?amed. Do not use Deep Relief Pain Relief Gel on: • children under 12 years old • your lips, nostrils, eyes, genital or anal areas, or other sensitive areas. If this occurs accidentally, wash away with plenty of clean water. • the same area with other medicines that you put on the skin. Deep Relief Pain Relief Gel is only for use on the skin. Do not take by mouth. Take special care with Deep Relief Pain Relief Gel See your doctor before using Deep Relief Pain Relief Gel if you: • have ever had allergic symptoms such as skin rashes or itching caused by medicines or cosmetics • have a kidney problem (now or in the past) • have a stomach ulcer (now or in the past) • are up to 6 months pregnant or think you might be pregnant • are having problems conceiving or having fertility treatment. Avoid getting Deep Relief Pain Relief Gel on or near the eyes and other sensitive areas. Taking other medicines Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines. This includes medicines you have bought without a prescription. See your doctor before using Deep Relief Pain Relief Gel if you are taking: • aspirin • any other pain relieving medicine • any other medicines regularly.

140mm Pregnancy and breast feeding See your doctor if you are pregnant or think you might be pregnant. Do not use Deep Relief Pain Relief Gel if you are more than 6 months pregnant. Do not use Deep Relief Pain Relief Gel if you are breast feeding. Ask your doctor or pharmacist for advice before taking any medicine. Important information about some of the ingredients of Deep Relief Pain Relief Gel Deep Relief Pain Relief Gel contains: • propylene glycol which may cause skin irritation.

3. How to use Deep Relief Pain Relief Gel Deep Relief Pain Relief Gel is for adults and children over 12 years old. • Always try on a small area ?rst. • If you have the 30 or 50g tube use 1-4 cm of gel each time you use Deep Relief Pain Relief Gel. If you have the 15g tube use 4-10 cm each time you use Deep Relief Pain Relief Gel. • Apply the gel as a thin layer over the a?ected area. • Gently rub in the gel until it is absorbed. You may notice a tingling sensation. • Do not use more gel than recommended. • Repeat these steps up to 3 times a day but no more. Do not use more often than every 4 hours. If the pain or swelling continues after using the gel for 2 weeks see your doctor. • Unless you are treating your hands always wash your hands immediately after use. • Replace the cap tightly. • Stop using Deep Relief Pain Relief Gel if you get excessive skin irritation or other unwanted e?ects. Do not cover the skin with bandages, plasters or any other dressing. However, it is safe to cover the skin with your clothes. If you use more Deep Relief Pain Relief Gel than you should If you accidently squeeze out too much gel use a tissue to wipe o? any excess. If you or a child accidentally swallow the gel contact your doctor or hospital immediately. If you forget to use Deep Relief Pain Relief Gel Apply Deep Relief Pain Relief Gel again when you remember making sure you do not use the gel more than 3 times in one day or more often than every 4 hours. 4. Possible side e?ects Like all medicines, Deep Relief Pain Relief Gel can cause side e?ects, although not everybody gets them. Stop using Deep Relief Pain Relief Gel straight away and tell your doctor if you experience any of the following e?ects: • unexplained wheezing • shortness of breath • blisters or a rash on the skin • itching, redness or bruising of the skin • swelling of the face

A slight redness, drying, tingling or burning feeling may occur where you have applied the gel. This is not a cause for concern. However, if this gets worse stop using Deep Relief Pain Relief Gel and tell your doctor. Unwanted e?ects may be reduced if you use the smallest dose for as short a time as possible. More rarely you may su?er from: • stomach pains or indigestion • kidney problems if you have kidney disease. Reporting of side e?ects If you get any side e?ects, talk to your doctor, pharmacist or nurse. This includes any possible side e?ects not listed in this lea?et. You can also report side e?ects directly via the Yellow Card Scheme at: www. mhra. gov. uk/yellowcard. By reporting side e?ects you can help provide more information on the safety of medicines. 5. How to store Deep Relief Pain Relief Gel Keep out of the sight and reach of children. Close the cap tightly and store in a cool place (below 25°C). Do not use Deep Relief Pain Relief Gel after the expiry date which is printed on the carton and tube. The ‘expiry’ date refers to the last day of that month. Take any Deep Relief Pain Relief Gel that is out of date to a pharmacist for disposal. 6. Further information What Deep Relief Pain Relief Gel contains The active substances are: • ibuprofen (5%w/w) • levomenthol (3%w/w) The other ingredients are propylene glycol, carbomer, diisopropanolamine, ethanol and water (see the end of Section 2). What Deep Relief Pain Relief Gel looks like and contents of the pack Deep Relief Pain Relief Gel is a clear gel. Each tube contains 15, 30 or 50g. Not all pack sizes may be marketed. Marketing authorisation holder and manufacturer:

The Mentholatum Company Limited, East Kilbride, G74 5PE, Scotland, UK. Tel: 01355 848484 PL 00189/0027 For any information about this product please contact the manufacturer at the above address. This lea?et was last revised January 2014

Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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