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Erectile dysfunction is the inability to get or keep an erection. ED usually has a physical cause.

LEVITRA helps improve erectile function by increasing blood flow to the penis. LEVITRA has helped many men and it may help you, too.

LEVITRA can cause your blood pressure to drop suddenly to an unsafe level if it is taken with certain other medicines. With a sudden drop in blood pressure, you could get dizzy, faint, or have a heart attack or stroke.

If, like millions of other men, you have noticed changes in your erections, you can do something about it. Talking to your doctor is the first step.

Did you know ED usually has a physical cause?

Erectle Dysfunction Treatment - LEVITRA See your doctor.

Indication LEVITRA is a prescription medicine used for the treatment of erectile dysfunction (ED) in men.

Important Safety Information

LEVITRA can cause your blood pressure to drop suddenly to an unsafe level if it is taken with certain other medicines. With a sudden drop in blood pressure, you could get dizzy, faint, or have a heart attack or stroke.

Do not take LEVITRA if you:

Take any medications called "nitrates" (often used to control chest pain, also known as angina), or if you use recreational drugs called "poppers" like amyl nitrate and butyl nitrate. Nitrates may cause abnormally low blood pressure and LEVITRA may increase that risk

Take riociguat (Adempas ® ), a guanylate cyclase stimulator . a medicine that treats pulmonary arterial hypertension and chronic-thromboembolic pulmonary hypertension

Have been told by your healthcare provider not to have sexual activity because of health problems. Sexual activity can put an extra strain on your heart, especially if your heart is already weak from a heart attack or heart disease

Tell all your healthcare providers that you take LEVITRA. If you need emergency medical care for a heart problem, it will be important for your healthcare provider to know when you last took LEVITRA.

LEVITRA does not protect a man or his partner from sexually transmitted diseases, including HIV.

Before taking LEVITRA, tell your doctor about all your medical problems, including if you:

have heart problems such as angina, heart failure, irregular heartbeats, or have had a heart attack—ask your doctor if it is safe for you to have sexual activity

have low blood pressure or have high blood pressure that is not controlled

have pulmonary hypertension

have had a stroke

have had a seizure

or any family members have a rare heart condition known as prolongation of the QT interval (long QT syndrome)

have liver problems

have kidney problems and require dialysis

have retinitis pigmentosa, a rare genetic (runs in families) eye disease

have ever had severe vision loss, or if you have an eye condition called non-arteritic anterior ischemic optic neuropathy (NAION)

have stomach ulcers

have a bleeding problem

have a deformed penis shape or Peyronie's disease

have had an erection that lasted more than 4 hours

have blood cell problems such as sickle cell anemia, multiple myeloma, or leukemia

have hearing problems

Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. LEVITRA and other medicines may affect each other. Especially tell your doctor if you take any of the following:

Ritonavir (Norvir ® ) or indinavir sulfate (Crixivan ® ), saquinavir (Fortavase ® or Invirase ® ) or atazanavir (Reyataz ® ), or other HIV protease inhibitors

Ketoconazole or itraconazole (such as Nizoral ® or Sporanox ® )

Erythromycin or clarithromycin

Tell your doctor if you take alpha-blockers. These include Hytrin ® (terazosin HCl), Flomax ® (tamsulosin HCl), Cardura ® (doxazosin mesylate), Minipress ® (prazosin HCl), Uroxatral ® (alfuzosin HCl), or Rapaflo ® (silodosin). Alpha-blockers are sometimes prescribed for prostate problems or high blood pressure. In some patients, the use of PDE5 inhibitor drugs, including LEVITRA, with alpha-blockers can lower blood pressure significantly, leading to fainting.

Contact the prescribing physician if alpha-blockers or other drugs that lower blood pressure are prescribed by another healthcare provider

Tell your doctor if you take medicines that treat abnormal heartbeat. These include quinidine, procainamide, amiodarone, and sotalol. Patients taking these drugs should not use LEVITRA.

Do not use LEVITRA with other medicines or treatments for ED.

Take LEVITRA exactly as your doctor prescribes. LEVITRA comes in different doses (2.5 mg, 5 mg, 10 mg, and 20 mg). For most men, the recommended starting dose is 10 mg. Do not take more than one tablet of LEVITRA per day. Doses should be taken at least 24 hours apart. Some men can take only a low dose of LEVITRA because of medical conditions or medicines they take. Your doctor will prescribe the dose that is right for you.

If you are older than 65 or have liver problems, your doctor may start you on a lower dose of LEVITRA

If you have prostate problems or high blood pressure for which you take medicines called alpha-blockers, your doctor may start you on a lower dose of LEVITRA

If you are taking certain other medicines, your doctor may prescribe a lower starting dose and limit you to one dose of LEVITRA in a 72-hour (3-day) period.

The most common side effects with LEVITRA are headache, flushing, stuffy or runny nose, indigestion, upset stomach, dizziness, and back pain.

LEVITRA may uncommonly cause:

An erection that lasts more than 4 hours . Get medical help right away to avoid lasting damage to your penis

Color vision changes . such as seeing a blue tinge to objects or having difficulty telling the difference between the colors blue and green

In rare instances, men taking PDE5 inhibitors (oral erectile dysfunction medicines, including LEVITRA) reported a sudden decrease or loss of vision in one or both eyes or a sudden decrease or loss in hearing, sometimes with ringing in the ears and dizziness. It is not possible to determine whether these events are related directly to the PDE5 inhibitors, to other diseases or medications, to other factors, or to a combination of factors. If you experience sudden decrease or loss of vision or hearing, stop taking LEVITRA and contact a doctor right away.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www. fda. gov/medwatch, or call 1-800-FDA-1088.

Please read the Patient Information and discuss it with your doctor.

The physician Prescribing Information is also available.

NOTE: All trademarks are the property of their respective owners.

?Adobe is a registered trademark of Adobe Systems incorporated.

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Decadron is used to treat conditions such as arthritis, blood/hormone/immune system disorders, allergic reactions, certain skin and eye conditions, breathing problems, certain bowel disorders. Also it is used in the treatment of cancers of the white blood cells (leukemias), and lymph gland cancers (lymphomas).

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Product Description Common use Decadron is used to treat conditions such as arthritis, blood/hormone/immune system disorders, allergic reactions, certain skin and eye conditions, breathing problems, certain bowel disorders. Also it is used in the treatment of cancers of the white blood cells (leukemias), and lymph gland cancers (lymphomas). Finally, Decadron is used as replacement therapy in patients whose adrenal glands are unable to produce sufficient amounts of corticosteroids.

Dosage and direction Take this medication by mouth as directed by your doctor. The initial oral dose is 0.75 to 9 mg daily depending on the disease. The initial dose should be adjusted according to the response to therapy. Take with food or milk to prevent stomach upset. Take this medication by mouth with food or a full glass of water or milk unless your doctor directs you otherwise. If you take this medication once daily, take it in the morning before 9 AM. Use this medication regularly in order to get the most benefit from it. Take it at the same time(s) each day. It is important to continue taking this medication even if you feel well. Follow the dosing schedule carefully, and take this medication exactly as prescribed. Do not stop taking this medication without consulting your doctor. Inform your doctor if your condition does not improve or worsens.

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Contraindications Do NOT use Decadron if you are allergic to any ingredient in Decadron, you have a systemic fungal infection, you are taking mifepristone. Contact your doctor or health care provider immediately if any of these apply to you.

Possible side effects

Side effects of Decadron depend on the dose, the duration and the frequency of administration. Short courses of dexamethasone usually are well tolerated with few and mild side effects. Long term, high dose dexamethasone usually will produce predictable and potentially serious side effects. Whenever possible, the lowest effective dose of dexamethasone should be used for the shortest possible length of time to minimize side effects. Alternate day dosing also can help reduce side effects. Side effects include fluid retention, weight gain, high blood pressure, loss of potassium, headache, muscle weakness, puffiness, and hair growth on the face, thinning and easy bruising of skin, glaucoma, cataracts, peptic ulceration, worsening of diabetes, irregular menses, growth retardation in children, convulsions, stomach upset, headache, dizziness, menstrual changes, trouble sleeping, increased appetite, or weight gain may occur, depression, euphoria, insomnia, mood swings, personality changes, and even psychotic behavior. A very serious allergic reaction to this drug is rare. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Drug interactions Drugs such as phenobarbital, ephedrine, phenytoin (Dilantin), and rifampin (Rifadin, Rimactane) may increase the breakdown of corticosteroids by the liver. As a result it may be lower blood levels and reduced effects. Therefore, the dose of corticosteroid may need to be increased if treatment with any of these agents is begun.

Missed dose If you are taking this medication daily and on a regular schedule, and 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.

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

Storage Decadron should be stored at 68-77 F (20-25 C) and not frozen

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.

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Ini adalah review terhadap obat dengan merk comsikla. di bagian akhir review ini juga disertakan tautan untuk mengetahui merk obat-obat lain dengan kandungan yang sama dengan comsikla.

golongan . obat keras

kemasan . botol 60 ml suspensi, dos 5 x 6 tablet forte

kandungan . (amoksisilin 500 mg + asam klavulanat 125 mg)/ tablet forte, (amoksisilin 125 mg + asam klavulanat 31.25 mg)/ 5 ml suspensi

Sekilas tentang zat aktif (generik name)

Coamoxiclav adalah antibiotik kombinasi antara Amoxicillin, antibiotik golongan ?-laktam dan asam klavulanat, penghambat enzim ?-laktamase. Kombinasi ini bertujuan untuk meningkatkan spektrum aksinya terhadap bakteri-bakteri yang memproduksi ?-laktamase yang resisten terhadap antibiotik amoxicillin. Coamoxiclav adalah bakteriolitik yang bekerja dengan cara menghambat sintesis dinding sel bakteri sehingga lintas hubungan antara rantai polimer peptidoglikan linier yang membentuk komponen utama dari dinding sel bakteri menjadi terganggu.

Indikasi comsikla

Kegunaan comsikla (Coamoxiclav ) adalah untuk mengobati infeksi yang disebabkan oleh kuman yang peka terhadap comsikla (Coamoxiclav ) seperti otitis media akut, faringitis yang disebabkan streptococcus . pneumonia, infeksi kulit, infeksi saluran kemih, infeksi Salmonella . Lyme disesase . dan infeksi klamidia. comsikla (Coamoxiclav ) juga digunakan untuk mencegah endokarditis yang disebabkan bakteri pada orang-orang berisiko tinggi saat perawatan gigi, untuk mencegah infeksi oleh Streptococcus pneumoniae dan infeksi bakteri lainnya. comsikla (Coamoxiclav ) sangat umum digunakan untuk infeksi saluran pernafasan bagian atas dan bawah, infeksi saluran kemih, saluran cerna, kulit dan jaringan lunak.

Kontra indikasi

comsikla (Coamoxiclav ) harus dihindari pada pasien hipersensitifitas pada comsikla (Coamoxiclav ) dan antibiotika penisillinum lainnya.

Efek Samping comsikla

kebanyakan efek samping comsikla (Coamoxiclav ) yang muncul adalah mual. muntah. ruam. dan antibiotik kolitis. kadang-kadang diare juga dapat terjadi. Efek samping yang jarang seperti perubahan mental, sakit kepala ringan. insomnia. kebingungan. kecemasan. kepekaan terhadap cahaya dan suara. dan berpikir tidak jelas. Perawatan medis harus segera diberikan jika tanda-tanda pertama dari efek samping muncul karena jika seseorang mengalami reaksi hipersensitivitas terhadap comsikla (Coamoxiclav ), dapat mengalami shock anafilaktik yang bisa berakibat fatal.

Perhatian

Hati-hati memberikan comsikla (Coamoxiclav ) pada penderita dengan fungsi hati dan ginjal yang rusak terutama pada pemakaian obat dalam jangka waktu panjang. Hentikan pemakaian comsikla (Coamoxiclav ) jika terjadi super infeksi yang biasanya terjadi pada saluran pencernaan (umumnya disebabkan Enterobacter . Pseudomonas, S. aureus Candida )

Toleransi terhadap kehamilan

Penelitian pada reproduksi hewan tidak menunjukkan risiko pemakaian Coamoxiclav pada janin dan tidak ada studi yang memadai dan terkendali dengan baik pada wanita hamil / Penelitian pada hewan telah menunjukkan efek buruk. namun studi yang memadai dan terkendali dengan baik pada ibu hamil tidak menunjukkan risiko untuk janin dalam trimester berapapun.

interaksi obat

comsikla (Coamoxiclav ) berinteraksi dengan obat-obat seperti. Antikoagulan (misalnya. warfarin. dabigatran ), Allopurinol ( pengobatan asam urat ), antibiotik tertentu, obat kanker ( methotrexate ), obat urikosurik, dan vaksin tifoid

Dosis comsikla

comsikla (Coamoxiclav ) diberikan dengan dosis. dewasa dan anak > 12 tahun. infeksi ringan sampai sedang 3 x sehari 250 mg, infeksi berat 3 x sehari 500 mg; anak < 12 tahun. 25-50 mg/ kg BB/hari; anak 7-12 tahun. 3 x sehari 10 ml syrup atau 5 ml syrup forte; anak 2 -7 tahun. 3 x sehari 5 ml syrup; anak 9 bulan - 2 tahun. 3 x sehari 2. 5 ml syrup. Untuk pasien dengan fungsi ginjal yang buruk, monitor kadar obat dalam plasma dan urine harus dilakukan.

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Buy fexofenadine hcl 180mg

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FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS

Transcript

PACKAGE LEAFLET: INFORMATION FOR THE USER Fexofenadine hydrochloride 180mg Film-coated Tablets Fexofenadine hydrochloride Read all of this leaflet carefully before you start taking this medicine because it contains important information for you. x Keep this leaflet. You may need to read it again. x If you have any further questions, ask your doctor or pharmacist. x This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. x If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. What is in this leaflet 1. What Fexofenadine hydrochloride 180mg Film-coated Tablets are and what they are used for 2. What you need to know before you take Fexofenadine hydrochloride 180mg Film-coated Tablets 3. How to take Fexofenadine hydrochloride 180mg Film-coated Tablets 4. Possible side effects 5. How to store Fexofenadine hydrochloride 180mg Film-coated Tablets 6. Contents of the pack and other information

1. WHAT FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS ARE AND WHAT THEY ARE USED FOR Fexofenadine hydrochloride 180mg film-coated Tablets contain Fexofenadine hydrochloride, which is an antihistamine. Fexofenadine hydrochloride 180mg film-coated Tablets are used in adults and adolescents of 12 years and older to relieve the symptoms that occur with long term allergic skin reactions (chronic idiopathic urticaria) such as itching, swelling and rashes. Fexofenadine hydrochloride 180 mg film-coated Tablets will also be referred to in this leaflet as Fexofenadine tablets.

2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS Do not take Fexofenadine Tablets x

If you are allergic to Fexofenadine hydrochloride or any of the other ingredients of this medicine listed in Section 6

Warnings and precautions Talk to your doctor or pharmacist before taking Fexofenadine tablets if you: x have problems with your liver or kidneys x have or ever had heart disease, since this kind of medicine may lead to a fast or irregular heart beat x are elderly If any of these apply to you, or if you are not sure, tell your doctor before taking Fexofenadine tablets.

Other medicines and Fexofenadine tablets Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Indigestion remedies containing aluminium and magnesium may affect the action of Fexofenadine tablets, by lowering the amount of medicinal product absorbed. It is recommended that you leave about 2 hours between the time that you take Fexofenadine tablets and your indigestion remedy.

Pregnancy and breast-feeding Ask your doctor or pharmacist for advice before taking any medicine. Do not take Fexofenadine hydrochloride 180mg Film-coated tablets if you are pregnant, unless necessary. Fexofenadine tablets are not recommended during breast-feeding.

Driving and using machines Fexofenadine tablets are unlikely to affect your ability to drive or operate machinery. However, you should check that these tablets do not make you feel sleepy or dizzy before driving or operating machinery.

3. HOW TO TAKE FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

For adults and children aged 12 years and over The recommended dose is one tablet (180mg) daily. Take your tablet with water before a meal.

If you take more Fexofenadine tablets than you should If you take too many tablets, contact your doctor or the nearest hospital emergency department immediately. Symptoms of an overdose in adults are dizziness, drowsiness, fatigue and dry mouth.

If you forget to take Fexofenadine tablets Do not take a double dose to make up for a forgotten tablet. Take the next dose at the usual time as prescribed by your doctor.

If you stop taking Fexofenadine tablets Tell your doctor if you want to stop taking Fexofenadine tablets before you have finished your course of treatment. If you stop taking Fexofenadine tablets earlier than planned, your symptoms may return. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. POSSIBLE SIDE EFFECTS Like all medicines, this medicine can cause side effects, although not everybody gets them. x

Tell your doctor immediately and stop taking Fexofenadine tablets if you experience:

swelling of the face, lips, tongue or throat and difficulty breathing, as these may be signs of a serious allergic reaction.

Common side effects (may affect up to 1 in 10 people):

headache drowsiness feeling sick (nausea) dizziness.

Uncommon side effects (may affect up to 1 in 100 people):

Additional side effects (frequency not known: cannot be estimated from the available data) which may occur are:

difficulty sleeping (insomnia) sleeping disorders bad dreams nervousness fast or irregular heart beat diarrhoea skin rash and itching hives serious allergic reactions which can cause swelling of the face, lips, tongue or throat, flushing, chest tightness, and difficulty breathing.

Reporting of side effects If you get any side effects talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: http://yellowcard. mhra. gov. uk/. By reporting side effects you can help provide more information on the safety of this medicine.

5. HOW TO STORE FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month. This medicine does not require any special storage condition. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. CONTENTS OF THE PACK AND OTHER INFORMATION What Fexofenadine Tablets contain The active substance is fexofenadine hydrochloride. Each film coated tablet contains 180mg of Fexofenadine hydrochloride; equivalent to 168mg of Fexofenadine. The other ingredients (Excipients) are: Tablet core: Powdered Cellulose, Mannitol (E421), Maize starch, Croscarmellose Sodium, Colloidal anhydrous Silica, Magnesium Stearate. Tablet coating: Opadry Pink film-coating mixture containing Hypromellose (E464), Titanium dioxide (E171), Macrogol 400, Allura Red AC Lake (FD&C Red #40) (E129), and Iron Oxide, Black (E172) What Fexofenadine hydrochloride 180mg film-coated Tablets look like and contents of the pack Fexofenadine hydrochloride 180mg film-coated Tablets are pink coloured, oval, tablets marked with “FXF” on one side and “180” on the other side. Fexofenadine tablets are packed in blister strips packaged in cartons. The cartons contain 20 or 30 Tablets. Not all packs may be marketed. Marketing Authorisation Holder and Manufacturer Dr. Reddy’s Laboratories (UK) Ltd, 6 Riverview Road, Beverley, HU17 0LD, UK. Fexofenadine hydrochloride 180mg film-coated Tablets: PL08553/0274 This leaflet was last revised in 07/2014

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.

fexofenadine 24-hour tablet - oral, Allegra

The display and use of drug information on this site is subject to express terms of use. By continuing to view the drug information, you agree to abide by such terms of use.

GENERIC NAME: FEXOFENADINE 24-HOUR TABLET - ORAL (FEX-oh-FEN-a-deen)

BRAND NAME(S): Allegra

USES: Fexofenadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose. itching eyes/nose, sneezing. hives. and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction .

HOW TO USE: If you are taking the over-the-counter product to self-treat, read all directions on the product package before taking this medication. If you have any questions, consult your pharmacist. If your doctor has prescribed this medication, take it as directed with or without food, usually once daily. Take this medication with water. Do not take with fruit juices (such as apple, grapefruit, or orange) since they may decrease the absorption of this drug. The dosage is based on your age, medical condition, and response to treatment. Do not increase your dose or take this medication more often than directed. Do not take antacids containing aluminum and magnesium within 2 hours of taking this medication. These antacids can decrease the absorption of fexofenadine. Tell your doctor if your condition does not improve or if it worsens.

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FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS

Transcript

PACKAGE LEAFLET: INFORMATION FOR THE USER Fexofenadine hydrochloride 180mg Film-coated Tablets Fexofenadine hydrochloride Read all of this leaflet carefully before you start taking this medicine because it contains important information for you. x Keep this leaflet. You may need to read it again. x If you have any further questions, ask your doctor or pharmacist. x This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. x If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. What is in this leaflet 1. What Fexofenadine hydrochloride 180mg Film-coated Tablets are and what they are used for 2. What you need to know before you take Fexofenadine hydrochloride 180mg Film-coated Tablets 3. How to take Fexofenadine hydrochloride 180mg Film-coated Tablets 4. Possible side effects 5. How to store Fexofenadine hydrochloride 180mg Film-coated Tablets 6. Contents of the pack and other information

1. WHAT FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS ARE AND WHAT THEY ARE USED FOR Fexofenadine hydrochloride 180mg film-coated Tablets contain Fexofenadine hydrochloride, which is an antihistamine. Fexofenadine hydrochloride 180mg film-coated Tablets are used in adults and adolescents of 12 years and older to relieve the symptoms that occur with long term allergic skin reactions (chronic idiopathic urticaria) such as itching, swelling and rashes. Fexofenadine hydrochloride 180 mg film-coated Tablets will also be referred to in this leaflet as Fexofenadine tablets.

2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS Do not take Fexofenadine Tablets x

If you are allergic to Fexofenadine hydrochloride or any of the other ingredients of this medicine listed in Section 6

Warnings and precautions Talk to your doctor or pharmacist before taking Fexofenadine tablets if you: x have problems with your liver or kidneys x have or ever had heart disease, since this kind of medicine may lead to a fast or irregular heart beat x are elderly If any of these apply to you, or if you are not sure, tell your doctor before taking Fexofenadine tablets.

Other medicines and Fexofenadine tablets Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Indigestion remedies containing aluminium and magnesium may affect the action of Fexofenadine tablets, by lowering the amount of medicinal product absorbed. It is recommended that you leave about 2 hours between the time that you take Fexofenadine tablets and your indigestion remedy.

Pregnancy and breast-feeding Ask your doctor or pharmacist for advice before taking any medicine. Do not take Fexofenadine hydrochloride 180mg Film-coated tablets if you are pregnant, unless necessary. Fexofenadine tablets are not recommended during breast-feeding.

Driving and using machines Fexofenadine tablets are unlikely to affect your ability to drive or operate machinery. However, you should check that these tablets do not make you feel sleepy or dizzy before driving or operating machinery.

3. HOW TO TAKE FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

For adults and children aged 12 years and over The recommended dose is one tablet (180mg) daily. Take your tablet with water before a meal.

If you take more Fexofenadine tablets than you should If you take too many tablets, contact your doctor or the nearest hospital emergency department immediately. Symptoms of an overdose in adults are dizziness, drowsiness, fatigue and dry mouth.

If you forget to take Fexofenadine tablets Do not take a double dose to make up for a forgotten tablet. Take the next dose at the usual time as prescribed by your doctor.

If you stop taking Fexofenadine tablets Tell your doctor if you want to stop taking Fexofenadine tablets before you have finished your course of treatment. If you stop taking Fexofenadine tablets earlier than planned, your symptoms may return. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. POSSIBLE SIDE EFFECTS Like all medicines, this medicine can cause side effects, although not everybody gets them. x

Tell your doctor immediately and stop taking Fexofenadine tablets if you experience:

swelling of the face, lips, tongue or throat and difficulty breathing, as these may be signs of a serious allergic reaction.

Common side effects (may affect up to 1 in 10 people):

headache drowsiness feeling sick (nausea) dizziness.

Uncommon side effects (may affect up to 1 in 100 people):

Additional side effects (frequency not known: cannot be estimated from the available data) which may occur are:

difficulty sleeping (insomnia) sleeping disorders bad dreams nervousness fast or irregular heart beat diarrhoea skin rash and itching hives serious allergic reactions which can cause swelling of the face, lips, tongue or throat, flushing, chest tightness, and difficulty breathing.

Reporting of side effects If you get any side effects talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: http://yellowcard. mhra. gov. uk/. By reporting side effects you can help provide more information on the safety of this medicine.

5. HOW TO STORE FEXOFENADINE HYDROCHLORIDE 180MG FILM-COATED TABLETS Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month. This medicine does not require any special storage condition. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. CONTENTS OF THE PACK AND OTHER INFORMATION What Fexofenadine Tablets contain The active substance is fexofenadine hydrochloride. Each film coated tablet contains 180mg of Fexofenadine hydrochloride; equivalent to 168mg of Fexofenadine. The other ingredients (Excipients) are: Tablet core: Powdered Cellulose, Mannitol (E421), Maize starch, Croscarmellose Sodium, Colloidal anhydrous Silica, Magnesium Stearate. Tablet coating: Opadry Pink film-coating mixture containing Hypromellose (E464), Titanium dioxide (E171), Macrogol 400, Allura Red AC Lake (FD&C Red #40) (E129), and Iron Oxide, Black (E172) What Fexofenadine hydrochloride 180mg film-coated Tablets look like and contents of the pack Fexofenadine hydrochloride 180mg film-coated Tablets are pink coloured, oval, tablets marked with “FXF” on one side and “180” on the other side. Fexofenadine tablets are packed in blister strips packaged in cartons. The cartons contain 20 or 30 Tablets. Not all packs may be marketed. Marketing Authorisation Holder and Manufacturer Dr. Reddy’s Laboratories (UK) Ltd, 6 Riverview Road, Beverley, HU17 0LD, UK. Fexofenadine hydrochloride 180mg film-coated Tablets: PL08553/0274 This leaflet was last revised in 07/2014

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.

Empecid - anti-infective agents, local, antifungal agents, growth inhibitors, atc a01ab18, atc d01ac

Empecid

Cream; Liquid; Solution; Suppository; Ointment; Lozenge

Empecid Indication

For the local treatment of oropharyngeal candidiasis and vaginal yeast infections, also used in fungal infections of the skin such as ringworm, athlete's foot, and jock itch.

Empecid Pharmacology

Clotrimazole, an imidazole derivative with a broad spectrum of antimycotic activity, inhibits biosynthesis of the sterol ergostol, an important component of fungal cell membranes. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane. Betamethasone and clotrimazole are used together to treat cutaneous tinea infections. In studies in fungal cultures, the minimum fungicidal concentration of clotrimazole caused leakage of intracellular phosphorous compounds into the ambient medium with concomitant breakdown of cellular nucleic acids, and accelerated potassium etflux. Both of these events began rapidly and extensively after addition of the drug to the cultures. The primary action of clotrimazole is against dividing and growing organisms.

Empecid Absorption

Poorly and erratically absorbed orally, minimal vaginal or topical absorption.

Empecid side effects and Toxicity

Symptoms of overdose include erythema, stinging, blistering, peeling, edema, pruritus, urticaria, burning, and general irritation of the skin, and cramps.

Empecid Patient Information

How to use Clotrimazole :Use clotrimazole exactly as directed by your doctor. Always read the manufacturer's information leaflet, if possible, before beginning treatment. Clotrimazole preparations are usually applied two to three times a day until the infection has cleared. This medicine is for you. Never give it to others, even if their condition appears to be the same as yours. Getting the most from your treatment. Always wash and dry your hands thoroughly before and after handling clotrimazole. Do not allow clotrimazole to come into contact with the eyes, ears, or mucous membranes (eg. mouth, vagina, inside of nose etc.), unless you are advised to do so by your doctor. Complete the full course of treatment with clotrimazole, otherwise your infection is likely to recur. Before using any 'over-the-counter' medicines, check with your pharmacist which medicines are safe for you to use alongside clotrimazole. You should see an improvement in your condition after a few days. If your condition does not seem to be getting better after seven days, consult your doctor for advice.

Empecid Organisms Affected

Yeast and other fungi

Alfaciclina, alfaciclina

Sumycin is used for treating infections caused by certain bacteria. Sumycin is a tetracycline antibiotic. It works by slowing the growth of sensitive bacteria by interfering with the production of proteins needed by the bacteria to grow. Slowing the bacteria's growth allows the body's defense mechanisms to destroy them.

Use Sumycin as directed by your doctor.

Take Sumycin by mouth on an empty stomach at least 1 hour before or 2 hours after eating.

Take Sumycin with a full glass of water (8 oz/240 mL). Do not lie down for 30 minutes after taking Sumycin.

If you also take antacids containing aluminum, calcium, or magnesium; preparations containing bismuth, iron, zinc, or sodium bicarbonate; or calcium rich foods (eg, milk, dairy products, calcium-enriched juices), do not take them within 2 to 3 hours before or after taking Sumycin. Check with your doctor if you have questions.

To clear up your infection completely, take Sumycin for the full course of treatment. Keep taking it even if you feel better in a few days.

If you miss a dose of Sumycin, 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 Sumycin.

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

Active Ingredient: Tetracycline hydrochloride.

Do NOT use Sumycin if:

you are allergic to any ingredient in Sumycin or other tetracycline antibiotics (eg, doxycycline)

you are taking acitretin or methoxyflurane.

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

Some medical conditions may interact with Sumycin. 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 diarrhea, a stomach infection, or kidney problems.

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

Acitretin or isotretinoin because side effects, such as increased pressure in the fluid surrounding the brain, may occur

Digoxin, methotrexate, methoxyflurane, or oral anticoagulants (eg, warfarin) because the risk of their side effects may be increased by Sumycin

Atovaquone, lithium, oral contraceptives (birth control pills), or penicillins (eg, amoxicillin) because their effectiveness may be decreased by Sumycin.

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

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

Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

Be sure to use Sumycin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Sumycin may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Sumycin. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

Do not use after expiration date. Outdated medicine is highly toxic to the kidneys.

Long-term or repeated use of Sumycin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

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

Lab tests may be performed while you use Sumycin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use of Sumycin in children may cause permanent discoloring of the teeth.

Sumycin should be used with extreme caution in children younger 8 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and beast-feeding: Sumycin has been shown to cause harm to the fetus. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Sumycin while you are pregnant. Sumycin is found in breast milk. Do not breast-feed while taking Sumycin.

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:

Black hairy tongue; blurred vision; bulky loose stools; diarrhea; difficulty swallowing; fever; headache; hives; hoarseness; indigestion; inflammation or redness of tongue; joint pain; loss of appetite; mouth sores; nausea; rash; sensitivity to sunlight; sore throat; stomach pain; swelling and itching of the rectum.

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); infection (fever, chills, sore throat); itching; nausea; severe skin reaction to the sun; vaginal irritation or discharge; 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.

Fexotabs tablets - drug info, indications, side effects, dosage, faq, fexotabs

Fexotabs Tablets

Indications and contraindications Fexotabs Tablets

FEXOTABS tablets contain an active ingredient called "fexofenadine". It is one of a group of medicines called antihistamines.

FEXOTABS 60 is used to relieve the symptoms of seasonal and perennial allergic rhinitis (including hayfever). FEXOTABS 120 and 180 are used to relieve the symptoms of hayfever (seasonal allergic rhinitis) such as sneezing, itchy, watery or red eyes, and itchy, blocked or runny nose. FEXOTABS 180 is also used to relieve the symptoms of urticaria otherwise known as hives or itchy rash.

FEXOTABS works by blocking the action of histamine which causes these unwanted effects.

FEXOTABS is a non-sedating antihistamine which means it has been shown not to make you drowsy or slow down your reactions.

Special precautions Fexotabs Tablets

You should inform your pharmacist/doctor if:

you are, or might be, pregnant

you are breast feeding

you have any allergies to any other medicines, foods, preservatives or dyes

you are taking other medicines

Your pharmacist/doctor will consider these points when recommending FEXOTABS.

Use in children:

There is currently not enough information available to recommend FEXOTABS for use in children under 12 years of age.

Take FEXOTABS with a glass of water. FEXOTABS may be taken with or without food.

For the relief of the symptoms of seasonal and perennial allergic rhinitis (including hayfever) the usual dosage for adults and children over 12 years is one FEXOTABS 60mg tablet twice daily, when required.

For the relief of the symptoms of hayfever, the usual dosage for adults and children over 12 years of age is one FEXOTABS 120mg tablet daily when required, or one FEXOTABS 180mg tablet daily when required.

For relief of the symptoms of urticaria, the usual dosage for adults and children over 12 years of age is one FEXOTABS 180mg tablet daily when required.

Do not take more than the recommended dose and remember, this medicine is for you. Do not give it to anyone else, even if their symptoms seem to be the same as yours.

If FEXOTABS does not relieve your symptoms, do not take extra tablets. Tell your doctor or pharmacist.

What do I do in case of Overdose?

If you think that you or someone else may have taken too much FEXOTABS - (even if there are no signs of discomfort or poisoning) - contact your doctor or Poisons Information Centre, or go to the Casualty Department at your nearest hospital.

Adverse and side effects Fexotabs Tablets

Tell your doctor or pharmacist as soon as possible if you do not feel well while taking FEXOTABS, even if you do not think the problem is connected with the medicine or is not listed in this leaflet.

All medicines can cause side effects. Although most people will not experience any, some of the side effects that may occur with FEXOTABS are:

These same effects were seen in patients taking dummy or placebo capsules during the clinical studies.

Do you have a question about Fexotabs Tablets?

Our experts have answered 13 questions about Fexotabs Tablets.

Most popular questions

Erythromycin (professional patient advice), etromycin

Erythromycin

Yosprala Yosprala (aspirin and omeprazole) is a platelet aggregation inhibitor and proton pump inhibitor.

Cuvitru Cuvitru (immune globulin subcutaneous (human)) is indicated as replacement therapy in the treatment.

Erelzi Erelzi (etanercept-szzs) is a tumor necrosis factor (TNF) blocker biosimilar to Enbrel indicated.

Troxyca ER Troxyca ER (oxycodone hydrochloride and naltrexone hydrochloride) is an extended-release.

FDA Consumer Updates

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Erphatrim dosis obat, erphatrim

erphatrim

Erphatrim adalah obat antibiotik yang digunakan untuk mengobati berbagai jenis infeksi seperti infeksi saluran pencernaan, pernafasan, saluran kemih dan berbagai jenis infeksi lainnya. Erphatrim mengandung cotrimoxazole, suatu obat antibiotik yang merupakan kombinasi trimethoprim dan sulfamethoxazole. Berikut ini adalah informasi lengkap Erphatrim yang disertai tautan merk-merk obat lain dengan nama generik yang sama.

pabrik

golongan

Harus dengan resep dokter

kemasan

Erphatrim dipasarkan dengan kemasan sebagai berikut :

dos 10 x 10 caplet

botol 1000 caplet

Tersedia juga sediaan-sediaan berikut :

kandungan

Tiap caplet Erphatrim mengandung zat aktif (nama generik) sebagai berikut :

trimethoprim 80 mg

sulfamethoxazole 400 mg

Sekilas tentang zat aktif (nama generik)

cotrimoxazole adalah antibiotik kombinasi trimethoprim dan sulfamethoxazole yang digunakan untuk mengobati berbagai macam infeksi bakteri. kombinasi ini dengan perbandingan satu bagian trimethoprim dan lima bagian sulfamethoxazole. Cotrimoxazole bekerja dengan cara menghambat enzim metabolisme asam folat pada bakteri yang peka. Trimethoprim sendiri adalah bakterisida sedangkan sulfamethoxazole adalah bakteriostatik. Dalam bentuk kombinasi, antibiotik ini berfungsi sebagai bakterisida. Cotrimoxazole bermanfaat untuk mengobati infeksi-infeksi oleh bakteri yang resisten sulfamethoxazole tapi masih peka terhadap trimethoprim.

Indikasi

Kegunaan Erphatrim (cotrimoxazole) adalah untuk pengobatan infeksi - infeksi berikut :

Infeksi saluran pernafasan. otitis media akut yang disebabkan oleh Streptococcus pneumoniae atau Haemophilus influenzae. Eksaserbasi akut bronchitis kronis yang disebabkan oleh pneumoniae atau H. influenzae, sebagai obat alternatif jika obat golongan penicillin tidak dapat digunakan.

Infeksi saluran pencernaan. sebagai pencegahan traveller diare yang disebabkan oleh bakteri E. coli, sebagai alternatif antibiotik golongan quinolon.

Infeksi saluran kemih. obat ini juga bermanfaat untuk pengobatan infeksi saluran kemih yang disebabkan bakteri coli, Klebsiella, Enterobacter, Morganella morganii, Proteus mirabilis, atau P. vulgaris.

Brucellosis dan kolera. obat ini adalah antibiotik alternatif untuk pengobatan brucellosis untuk pasien yang tidak bisa menggunakan tetracycline (misalnya anak-anak).

Infeksi mikobakteri. infeksi kulit yang disebabkan oleh Mycobacterium marinum juga bisa menggunakan antibiotik ini.

Pertusis. sebagai alternatif erythromycin.

Demam tifus dan infeksi Salmonella lain. umumnya demam tifus diobati dengan antibiotik golongan quinolon atau cephalosporin generasi ketiga seperti ceftriaxone dan cefotaxime, namun cotrimoxazole sering digunakan sebagai alternatifnya.

Selengkapnya lihat dosis.

Kontra indikasi

jangan menggunakan Erphatrim untuk pasien yang memiliki riwayat alergi terhadap trimethoprim dan sulfamethoxazole, atau obat-obat golongan sulfonamide lainnya).

Penggunaan obat ini untuk pasien dengan gangguan hati dan ginjal yang berat sebaiknya dihindari.

Jangan digunakan untuk wanita hamil terutama menjelang kelahiran, anak < 2 tahun (kecuali untuk pengobatan atau pencegahan pneumocytosis jiroveci (P. carinii) pada bayi dari usia empat minggu atau lebih).

Obat ini diketahui ikut keluar bersama air susu ibu, oleh karena itu pemakaian selama menyusui sebaiknya dikonsultasikan pada dokter.

Efek Samping

Berikut adalah beberapa efek samping yang mungkin terjadi saat menggunakan antibiotik ini :

Efek samping Erphatrim (cotrimoxazole) yang umum seperti mual, muntah, ruam, diare. demam, gatal nyeri otot dan sendi.

Reaksi alergi yang parah bisa terjadi bagi orang-orang yang sensitif terhadap obat-obat golongan sulfonamide termasuk Erphatrim (cotrimoxazole), seperti sindrom stevens-johnson, nekrolisis epidermal toksik, nekrosis hati fulminan, agranulositosis, anemia aplastik, dan diskrasia darah lainnya.

Hati-hati terhadap kemungkinan super infeksi pada saluran pencernaan yang disebabkan oleh pertumbuhan berlebihan jamur atau bakteri pada pencernaan.

Obat ini bisa menyebabkan hemolisis pada pasien yang kekurangan enzim glukosa-6-fosfat dehidrogenase (enzim yang berperan dalam produksi sel darah merah), terutama jika diberikan pada dosis yang tinggi.

Pada pasien lanjut usia, efek samping lebih rentan terjadi misalnya penekanan sumsum tulang dan penurunan trombosit (terutama jika obat ini diberikan bersamaan dengan diuretik jenis tiazid).

Perhatian

Hal-hal yang harus diperhatikan saat menggunakan obat ini adalah sebagai berikut :

Erphatrim (cotrimoxazole) harus dihentikan jika tanda-tanda awal reaksi alergi seperti ruam, gatal, sakit tenggorokan, demam, arthralgia, pucat, atau tanda-tanda lainnya muncul, karena jika terjadi bisa berakibat fatal.

Obat ini harus digunakan secara hati-hati pada pasien yang mempunyai penyakit asma bronkial.

Orang-orang yang kekurangan folat seperti pasien lanjut usia, pecandu alkohol, sedang menggunakan obat anti konvulsan, atau oang-orang yng mengalami malnutrisi, jika menggunakan Erphatrim (cotrimoxazole) harus mendapatkan perhatian serius.

seperti antibiotik lainnya obat ini harus digunakan sampai dosis yang disarankan habis. Jangan menghentikan pemakaian sebelum waktunya untuk menghindari terjadinya resistensi.

Pasien yang menggunakan antibiotik ini harus mengkonsumsi cukup cairan untuk mencegah kristaluria.

Toleransi terhadap kehamilan

FDA (badan pengawas obat dan makanan amerika serikat) mengkategorikan cotrimoxazole kedalam kategori C dengan penjelasan sebagai berikut :

Penelitian pada reproduksi hewan telah menunjukkan efek buruk pada janin dan tidak ada studi yang memadai dan terkendali dengan baik pada manusia, namun jika potensi keuntungan dapat dijamin, penggunaan obat pada ibu hamil dapat dilakukan meskipun potensi resiko sangat besar.

Hasil studi pada hewan tidak selalu bisa dijadikan ukuran keamanan penggunaan obat pada manusia. Oleh karena penelitian secara klinis yang terkendali dengan baik belum dilakukan, penggunaan obat-obat yang mengandung cotrimoxazole oleh ibu hamil harus dikonsultasikan dengan dokter.

Baca dosis dan interaksi antibiotik ini jika digunakan dengan obat-obat lain di halaman berikutnya…

Dorzolamide eye drops for glaucoma, dorzolamide

Dorzolamide eye drops for glaucoma (Trusopt)

Eye drops (these contain a preservative), and single-dose units (these are preservative-free)

An increase in pressure within your eye can lead to damage to the optic nerve at the back of your eye. When this occurs it is called glaucoma. Glaucoma can lead to a loss of vision if it is not treated. If you have an increased pressure within your eye but without any damage to the optic nerve, this is called ocular hypertension. People with ocular hypertension have an increased risk of later developing glaucoma. Treatment with dorzolamide eye drops helps to reduce eye pressure in people with ocular hypertension, and to prevent further eye damage in people with glaucoma.

Dorzolamide works by blocking the action of an enzyme called carbonic anhydrase. Blocking this enzyme reduces the amount of fluid that you make in the front part of your eye (called aqueous humour), and this helps to lower the pressure within your eye.

Sometimes, more than one type of eye drop is needed to keep the pressure in the eye low. If this is the case for you, you may be asked to use two different eye drops, or you may be given drops which combine more than one type. Dorzolamide is available as a combination eye drop with a beta-blocker called timolol, in a brand called Cosopt®.

Related discussions

Timolol eye drops side effects

Before using dorzolamide

Some medicines are not suitable for people with certain conditions, and sometimes a medicine may only be used if extra care is taken. For these reasons, before you start using the drops it is important that your doctor knows:

If you wear soft contact lenses.

If you are pregnant or breast-feeding.

If you have any problems with the way your kidneys work, or if you have ever had kidney stones.

If you have any problems with the way your liver works.

If you have a condition where your blood acidity is too high, called hyperchloraemic acidosis.

If you are taking any medicines. This includes any medicines you are taking which are available to buy without a prescription, such as herbal and complementary medicines.

If you have ever had an allergic reaction to a medicine. It is particularly important that you tell your doctor if you have ever had a bad reaction to any other eye drops, or to a type of medicine known as a 'sulfonamide'.

How to use dorzolamide eye drops

Wash your hands before you use the drops.

Remove the cap (or the tip of the unit if you are using a single-dose unit).

Tilt your head back a little and pull the lower lid of your eye out to form a pocket.

Hold the bottle (or single-dose unit) upside down near to your eye. Try not to touch your eye as you do this.

Press the container gently to release one drop into your eye. Only use a second drop if the first drop missed going into your eye.

Close your eye for a minute or two, and press gently on the side of your nose where the corner of your eye meets your nose. This helps to stop the drop from draining away and keeps it in your eye.

Repeat the process in your other eye if you have been told to use the drops in both eyes.

Replace the cap (or if you are using the single-dose unit, throw it away).

Getting the most from your treatment

Before you start using the eye drops, read the manufacturer's printed information leaflet from the pack. It will give you more information about the eye drops and will provide you with a full list of the side-effects which you may experience from using them.

Use one drop into the eye (or eyes) affected. The drops are used two or three times each day, depending on whether you are also using other drops. Your doctor will tell you how many times a day is right for you and your dose will also be printed on the label of the pack.

Remember to use the drops at regular intervals and try not to miss any doses. If you do forget to use the drops, put them in as soon as you remember, but do not 'double up' to make up for any missed doses.

Take care not to touch the tip of the dropper with your eye, fingers, or any other surface. This is to prevent the drops from becoming contaminated.

If you are using any other eye drops, leave 5-10 minutes between applying each one. This is to prevent more liquid going into your eye than it can handle. Otherwise the drops will overflow from your eye and not have the intended effect.

When first put in, eye drops can make your eyes water and may sometimes cause blurred vision. If this happens, it should quickly clear. Make sure you can see clearly again before you drive, or use tools or machines.

Do not wear soft contact lenses unless your doctor has advised you otherwise. This is because bottles of eye drops contain preservatives which can affect soft contact lenses. The single-dose units do not contain a preservative.

Keep your regular appointments with your doctor and eye clinic so that your progress can be checked.

If you are having an operation or any medical treatment, remember to tell the person carrying out the treatment that you are using dorzolamide eye drops.

Can dorzolamide eye drops cause problems?

Along with their useful effects, eye drops can cause unwanted side-effects although not everyone experiences them. The table below contains the most common ones associated with dorzolamide. You will find a full list in the manufacturer's information leaflet supplied with the drops. The unwanted effects often improve as your body adjusts to the new medicine, but speak with your doctor or pharmacist for further advice if any of the following continue or become troublesome.

Common dorzolamide side-effects

What can I do if I experience this?

Clarithromycin uses, dosage - side effects, clarithromycine

Clarithromycin

porphyria (a genetic enzyme disorder that causes symptoms affecting the skin or nervous system);

an electrolyte imbalance (such as low levels of potassium or magnesium in your blood);

a family history of Long QT syndrome; or

if you take certain heart rhythm medicine--amiodarone, disopyramide, dofetilide, flecainide, dronedarone, ibutilide, mexiletine, procainamide, propafenone, quinidine, or sotalol.

FDA pregnancy category C. It is not known whether clarithromycin will harm an unborn baby. Tell your doctor if you are pregnant or if you become pregnant while using this medicine.

In animal studies, clarithromycin caused birth defects. However, very high doses are used in animal studies. It is not known whether these effects would occur in people using regular doses. Ask your doctor about your risk.

Clarithromycin can pass into breast milk and may harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Do not give this medicine to a child younger than 6 months of age.

How should I take clarithromycin?

Take clarithromycin exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

You may take the tablets and oral suspension (liquid) with or without food.

Clarithromycin extended-release tablets (Biaxin XL) should be taken with food.

Do not crush, chew, or break an extended-release tablet . Swallow it whole.

Shake the oral suspension (liquid) well just before you measure a dose. Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one.

Use this medicine for the full prescribed length of time. Clarithromycin is usually given for up to 7 to 14 days. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Clarithromycin will not treat a viral infection such as the flu or a common cold.

Store at room temperature away from moisture and heat. Keep the bottle tightly closed when not in use.

Do not keep the oral liquid in a refrigerator. Throw away any liquid that has not been used within 14 days.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include severe stomach pain, nausea, vomiting, or diarrhea.

What should I avoid while taking clarithromycin?

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, stop taking this medicine and call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to.

Clarithromycin side effects

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

Call your doctor at once if you have:

headache with chest pain and severe dizziness, fast or pounding heartbeats, shortness of breath, fainting;

diarrhea that is watery or bloody;

fever, swollen glands, body aches, flu symptoms, new or worsening cough;

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

problems with your hearing;

signs of a kidney problem--little or no urinating; painful or difficult urination; swelling in your feet or ankles; feeling tired or short of breath; or

severe skin reaction--fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Older adults may be more likely to have heart rhythm side effects, including a life-threatening fast heart rate.

Clarithromycin may also cause severe liver symptoms. Stop taking clarithromycin and call your doctor at once if you have any of these liver symptoms:

itching, tired feeling;

nausea, upper stomach pain, loss of appetite;

dark urine, clay colored stools; or

jaundice (yellowing of the skin or eyes).

Common clarithromycin side effects may include:

stomach pain, indigestion, gas;

vomiting, mild diarrhea;

unusual or unpleasant taste in your mouth;

headache, sleep problems (insomnia);

mild itching or rash; or

vaginal itching or discharge.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect clarithromycin?

Many drugs can interact with clarithromycin. Not all possible interactions are listed here. Tell your doctor about all your medications and any you start or stop using during treatment, especially:

Cefuroxime - oral (ceftin) side effects, medical uses, and drug interactions, xorimax

cefuroxime - oral, Ceftin

GENERIC NAME: CEFUROXIME - ORAL (seff-you-ROX-eem)

BRAND NAME(S): Ceftin

USES: Cefuroxime is used to treat a wide variety of bacterial infections. This medication is known as a cephalosporin antibiotic. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (e. g. common cold. flu ). Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness.

HOW TO USE: Take this medication by mouth usually twice daily, or as directed by your doctor. Take cefuroxime with food to increase absorption and reduce stomach upset. Dosage is based on your medical condition and response to therapy. Swallow the tablets whole. Do not crush or chew because the tablets have a strong bitter taste. Use the liquid suspension form of this medication if it is difficult to swallow the tablets. Antibiotics work best when the amount of medicine in your body is kept at a constant level. Therefore, take this drug at evenly spaced intervals. Continue to take this medication until the full-prescribed amount is finished, even if symptoms disappear after a few days. Stopping the medication too early may allow bacteria to continue to grow, which may result in a relapse of the infection. Inform your doctor if your condition persists or worsens.

SIDE EFFECTS: Nausea. vomiting. diarrhea. or stomach pain may occur. Dizziness and drowsiness may occur less frequently, especially with higher doses. If any of these effects persist or worsen, notify 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 immediately if any of these unlikely but serious side effects occur: unusual tiredness /weakness. Tell your doctor immediately if any of these rare but very serious side effects occur: yellowing of the eyes/skin, severe stomach/abdominal pain. persistent nausea /vomiting. dark urine. change in the amount of urine, signs of new infection (e. g. fever. persistent sore throat ), easy bruising/bleeding, jerky movements, chest pain. mental/mood changes (such as confusion ).This medication may rarely cause a severe intestinal condition (Clostridium difficile - associated diarrhea ) due to a resistant bacteria. This condition may occur while receiving therapy or even weeks to months after treatment has stopped. Do not use anti-diarrhea products or narcotic pain medications if you have the following symptoms because these products may make them worse. Tell your doctor immediately if you develop: persistent diarrhea, abdominal or stomach pain /cramping, blood/mucus in your stool. Use of this medication for prolonged or repeated periods may result in oral thrush or a new vaginal yeast infection (oral or vaginal fungal infection). Contact your doctor if you notice white patches in your mouth, a change in vaginal discharge or other new symptoms. A very serious allergic reaction to this drug is unlikely, but seek immediate medical attention if it occurs. Symptoms of a serious allergic reaction may include: 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. In the US - Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Quick Guide Infectious Mononucleosis (Mono): Symptoms and Treatment

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.

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, except 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 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.

Need help identifying pills and medications?

Lamez od 50mg tablet 10s price, side-effects, uses generic-alternatives & dosage of lamez od 50mg ta

LIPAGLYN 4 mg. Pack of 10 Tablets

Side Effects of Lamictal 50mg Tablet 14s:

Skin eruptions usually maculopapular in nature, nausea, headache, tiredness, dizziness, ataxia, irritability/aggression, tremor, agitation, confusion, hallucination, diplopia, blurred vision. Haematological abnormalities e. g. leucopenia and thrombocytopenia. Elevations of LFTs. Arthralgia, pain and back pain. Potentially Fatal: Stevens-Johnson syndrome and toxic epidermal necrolysis.

Drug Interactions of Lamictal 50mg Tablet 14s:

Metabolism enhanced by enzyme-inducing drugs e. g. phenytoin, carbamazepine, phenobarbitone, primidone, rifampicin, ethinyloestradiol/levonorgestrel combination. Metabolism reduced by sodium valproate.

Contraindications of Lamictal 50mg Tablet 14s:

Mechanism of Action of Lamictal 50mg Tablet 14s:

Lamotrigine inhibits voltage-sensitive sodium channels, thereby stabilising neuronal membranes and consequently inhibiting pathological release of excitatory amino acids (e. g. glutamate and aspartate). These amino acids play a role in the generation and spread of epileptic seizures. Absorption: Well absorbed from the GI tract (oral); peak plasma concentrations after 2.5 hr. Distribution: Widely distributed; enters breast milk. Metabolism: Extensively hepatic. Excretion: Via urine (as glucuronide conjugate); 24 hr (elimination half-life at steady state).

Special Precautions for Lamictal 50mg Tablet 14s:

Hepatic or renal impairment. Closely monitor patient. Monitor children's body wt. Advise patient to report any hypersensitivity reaction. Avoid abrupt withdrawal unless severe skin reactions have developed. May impair ability to drive or operate machinery. Pregnancy and lactation.

Categories

Diclo-k, diclo-k

CARACTERÍSTICAS: DICLO-K es un analgésico, antiinflamatorio y antipirético no esteroideo de acción rápida, potente y duradera. Esta eficaz característica la pone de manifiesto al inhibir la conversión del ácido araquidónico en prostaglandinas, las cuales desempeñan un importante papel como mediadoras de la inflamación, el dolor y la fiebre. Se ha demostrado que DICLO-K es un potente inhibidor de la ciclooxigenasa, una enzima del complejo prostaglandina sintetasa, por lo que se requieren concentraciones mínimas de DICLO-K para obtener una acción analgésica, antiinflamatoria y antipirética eficaz.

Además de que las formas líquidas del diclofenaco se absorben por completo, en DICLO-K el sodio del diclofenaco sódico ha sido reemplazado por el ion potásico, lo que le confiere en el humano una más rápida y completa absorción, como se ha demostrado en estudios clínicos multicéntricos donde las concentraciones máximas en el plasma (T máx. ) se lograron 20 minutos después de la ingestión del medicamento (esto es válido en la presentación de comprimidos). La ingestión del medicamento (esto es válido en la presentación de comprimidos). La ingestión concomitante de alimentos no modifica la tasa ni el grado de absorción de DICLO-K, aunque su absorción es completa, su biodisponibilidad es de 50% al tener un sustancial metabolismo del primer paso por el hígado. Se une en algún grado a las proteínas plasmáticas (99,7%); la vida media es de 1-2 horas.

Se excreta 60% con la orina como metabolito y 1% en forma inalterada y el resto con las heces fecales. La edad no modifica fundamentalmente la farmacocinética de este producto.

Para el tratamiento sintomático a largo plazo en: Artritis reumatoide, osteoartritis y espondilitis anquilosante.

Para tratamiento a corto plazo en:

Estados dolorosos inflamatorios postraumáticos.

Inflamaciones y dolores posquirúrgicos.

Estados dolorosos y/o inflamatorios en ginecología (dismenorrea primaria anexitis).

Síndromes dolorosos de la columna vertebral.

Reumatismo no articular.

Como fármaco coadyuvante: En infecciones inflamatorias y dolorosas agudas de oídos, nariz y garganta. Procesos febriles elevados.

Hipersensibilidad a la sustancia activa y a otro analgésico-antiinflamatorio no esteroide inhibidor de la prostaglandina sintetasa.

Asma, urticaria, rinitis aguda o algún tipo de atopía dérmica luego de la administración del ácido acetilsalicílico.

Por lo general, DICLO-K es bien tolerado; ocasionalmente puede presentarse con la ingestión del mismo, epigastralgia, náuseas, vómito y diarrea. El sangramiento gastrointestinal y la úlcera péptica pueden aparecer esporádicamente. Con menos frecuencia se presentan cefalea, mareo y vértigo o somnolencia. En casos aislados, se pueden presentar insuficiencia renal aguda, nefritis intersticial, síndrome nefrótico, alteraciones funcionales del hígado, incluyendo hepatitis, discrasia sanguínea, exantema, urticaria, erupciones vesiculares, eccema y eritema multiforme.

La exactitud diagnóstica y vigilancia son imperativas en pacientes con síntomas de enfermedad gastrointestinal (úlcera gastroduodenal) enfermedad hepática o renal. Si hay úlcera péptica o hemorragia gastrointestinal debe suspenderse la administración de DICLO-K. Se debe valorar el uso del diclofenaco en el paciente con flujo o filtración renal afectada, tomando en cuenta el papel que juegan las prostaglandinas en el flujo sanguíneo renal, por igual en presencia de función hepática afectada por trastornos como la hepatitis, ya que este medicamento tiene un metabolismo de primer paso en el hígado. Durante el embarazo, DICLO-K se utiliza por razones muy poderosas en la más baja dosis efectiva. (Tomando en cuenta lo frecuente de un embarazo durante la adolescencia temprana y media). Como en el caso de otros analgésicos antiinflamatorios no esteroideos, éste se aplica especialmente en los últimos tres meses de embarazo, debido a la posibilidad de inercia uterina y/o cierre prematuro del ductus arterioso. A la dosis habitual de 50 mg cada 8 horas, las concentraciones son tan pequeñas que no se esperan efectos adversos en el bebé. Los pacientes que experimentan vértigo u otras alteraciones del Sistema Nervioso Central, deberán abstenerse de conducir vehículos u operar maquinarias.

INTERACCIONES MEDICAMENTOSAS: Cuando DICLO-K se administra junto con litio o digoxina, la concentración plasmática de DICLO-K puede aumentar. La administración concomitante de varios analgésicos antiinflamatorios no esteroideos pueden aumentar la ocurrencia de efectos secundarios. DICLO-K no influye sobre el efecto de los anticoagulantes; sin embargo cuando se utilizan juntos estos compuestos deben vigilarse muy de cerca si la acción del anticoagulante se mantiene. En dosis de 200 mg de DICLO-K puede, temporalmente, inhibir la agregación plaquetaria.

No hay interferencia de DICLO-K sobre el efecto clínico de los antidiabéticos orales. Se debe tener precaución con el uso de DICLO-K, antes o después de administrar metotrexato, ya que las concentraciones de este último pueden elevarse y aumentar la toxicidad del mismo.

SUPOSITORIOS: La absorción del diclofenaco potásico en esta presentación es rápida. Luego de la administración de supositorios de 12,5 mg, se obtiene un pico de las concentraciones en plasma en un intervalo de una hora, el comportamiento farmacocinético no varía tras la administración repetida. No se produce acumulación si se respetan los intervalos entre dosis recomendadas.

Adultos: Como norma, la dosis diaria inicial para adultos es de 100 a 200 mg. En casos leves como para niños mayores de 14 años la dosis diaria es de 50 a 100 mg es suficiente. La dosis debe fraccionarse en 2-3 tomas. En caso de dismenorrea primaria la dosis diaria debe adaptarse individualmente, varía, por lo general, de 50 a 150 mg. Inicialmente, se recomienda una dosis de 50-100 mg y en caso de ser necesario aumentaría gradualmente, durante varios ciclos hasta dar el máximo de 200 mg por día. Los comprimidos se deberán ingerir con líquido, preferiblemente antes de las comidas.

Gotas pediátricas: Niños mayores de 1 año de edad: 0,5 a 2 mg/kg, repartidas en 2-3 dosis orales. En casos de artritis reumatoide, la dosis puede elevarse a 3 mg/kg/día. Se recomienda agitar el envase antes de usarlo.

Suspensión pediátrica. A partir de los 5 años de edad y con un peso corporal mayor de 18 kg, de 0,5 a 2 mg/kg de peso corporal al día, repartidos en 3 dosis vía oral.

SOBREDOSIS: El tratamiento de la intoxicación por agentes analgésicos antiinflamatorios no esteroides, consiste en la aplicación de medidas de apoyo y síntomas. No hay un cuadro típico que resulte de una sobredosis de DICLO-K. Los pasos a seguir en caso de que se presente esta complicación es la siguiente:

1. Lavado gástrico.

2. Tratamiento con carbón activado.

3. Terapia de apoyo en caso de hipotensión, insuficiencia renal, convulsiones, irritación gastrointestinal y depresión respiratoria.

Comprimidos de 50 y 100 mg: Caja x 100.

Frasco-gotero con 16 ml.

Suspensión: Frasco de 60 ml.

Producto medicinal. Requiere receta médica.

Mantener fuera del alcance de los niños.

Mantener a temperatura no mayor de 30 °C.

Protéjase de la luz.

Laboratorio Rowe, C. por A.

Ketrel, ketrel

Ketrel

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