Tamiflu

In the US, Tamiflu (oseltamivir systemic) is a member of the drug class neuraminidase inhibitors and is used to treat Avian Influenza, Influenza, Influenza Prophylaxis and Swine Flu.

US matches:

• Tamiflu


• Tamiflu Suspension

UK matches:

• Tamiflu 12 mg/ml powder for oral suspension (SPC)
• Tamiflu 30 mg and 45 mg Hard Capsules (SPC)
• Tamiflu 75mg hard capsule (SPC)

Ingredient matches for Tamiflu

Oseltamivir

Oseltamivir is reported as an ingredient of Tamiflu in the following countries:

• Colombia


• Ecuador


• South Africa


• Turkey

Oseltamivir phosphate (a derivative of Oseltamivir) is reported as an ingredient of Tamiflu in the following countries:

• Algeria


• Argentina


• Australia


• Austria


• Bahrain


• Belgium


• Brazil


• Canada


• Chile


• China


• Croatia (Hrvatska)


• Czech Republic


• Denmark


• Finland


• France


• Georgia


• Germany


• Greece


• Hong Kong


• Hungary


• Iceland


• Ireland


• Israel


• Italy


• Japan


• Kuwait


• Lithuania


• Luxembourg


• Malaysia


• Mexico


• Morocco


• Netherlands


• New Zealand


• Norway


• Oman


• Philippines


• Poland


• Portugal


• Qatar


• Romania


• Russian Federation


• Saudi Arabia


• Serbia


• Singapore


• Slovakia


• Slovenia


• South Korea


• Spain


• Sri Lanka


• Sweden


• Switzerland


• Taiwan


• Thailand


• Ukraine


• United Arab Emirates


• United Kingdom


• United States


• Uruguay


• Venezuela


• Vietnam

International Drug Name Search

Glossary

SPC	Summary of Product Characteristics (UK)

Click for further information on drug naming conventions and International Nonproprietary Names.

Stridex Body Focus Cream

Pronunciation: sal-ih-SILL-ik AS-id
Generic Name: Salicylic Acid
Brand Name: Examples include Fostex and Stridex Body Focus

Stridex Body Focus Cream is used for:

Treating acne. It may also be used for other conditions as determined by your doctor.

Stridex Body Focus Cream is a topical salicylate. It works by causing the skin to swell, soften, and then slough or peel in areas where it is applied.

Do NOT use Stridex Body Focus Cream if:

• you are allergic to any ingredient in Stridex Body Focus Cream

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

Before using Stridex Body Focus Cream:

Some medical conditions may interact with Stridex Body Focus Cream. 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 had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to aspirin or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)


• if you have liver or kidney problems, a skin infection, skin irritation, diabetes, or poor blood circulation

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

• Anticoagulants, (eg, heparin, warfarin), aspirin, methotrexate, or sulfonylureas (eg, glipizide) because the risk of side effects may be increased by Stridex Body Focus Cream

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

Use Stridex Body Focus Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Wash and thoroughly dry the affected area. Apply a thin layer of Stridex Body Focus Cream to cover the entire affected area. Gently rub the medicine in until it is evenly distributed. Unless your hands are being treated, be sure to wash your hands after each use.


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

Ask your health care provider any questions you may have about how to use Stridex Body Focus Cream.

Important safety information:

• Stridex Body Focus Cream is for external use only. Avoid getting Stridex Body Focus Cream in your eyes, nose, or mouth, or on the genitals. If contact with your eyes occurs, flush with water for 15 minutes. Do not inhale the vapors of Stridex Body Focus Cream.


• Overuse of topical products may worsen your condition.


• Do not use Stridex Body Focus Cream longer or more often than recommended by your doctor or on the package label.


• Check with your doctor before use if you have a condition that covers a large area of the body.


• Be sure to apply Stridex Body Focus Cream only to the affected area and not to normal healthy skin.


• Do not use Stridex Body Focus Cream on skin that is irritated, infected, or reddened.


• Do not use Stridex Body Focus Cream on open skin wounds, moles, birthmarks, genital warts, warts on the face, or warts growing hair.


• Do not use any other medicines or drying products on your skin unless your doctor instructs you otherwise.


• Stridex Body Focus Cream may interfere with certain lab test results. Make sure your doctor and lab personnel know you are using Stridex Body Focus Cream.


• Stridex Body Focus Cream is extremely flammable. Do not store or use Stridex Body Focus Cream near a fire or other open flame.


• Stridex Body Focus Cream may be harmful if swallowed. If you may have taken Stridex Body Focus Cream by mouth, contact your local poison control center or emergency room immediately.


• Stridex Body Focus Cream contains a salicylate, which has been linked to Reye syndrome. Do not use Stridex Body Focus Cream on children or teenagers during or after chickenpox, flu, or other viral infections without checking with your doctor or pharmacist.


• Caution is advised when using Stridex Body Focus Cream in CHILDREN because they may be more sensitive to its effects.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Stridex Body Focus Cream during pregnancy. It is unknown if Stridex Body Focus Cream is excreted in breast milk. Do not breast-feed while you are using Stridex Body Focus Cream.

Possible side effects of Stridex Body Focus Cream:

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:

Dry, peeling, red, or scaling skin.

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); severe irritation.

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.

See also: Stridex Body Focus side effects (in more detail)

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 agitation; diarrhea; dizziness; loss of appetite; loss of hearing; mental disturbances; nausea; rapid or difficult breathing; ringing in the ears; seizures; sluggishness; vomiting; yellowing of the skin or eyes.

Proper storage of Stridex Body Focus Cream:

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

General information:

• If you have any questions about Stridex Body Focus Cream, please talk with your doctor, pharmacist, or other health care provider.


• Stridex Body Focus Cream 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 is a summary only. It does not contain all information about Stridex Body Focus Cream. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Stridex Body Focus resources

• Stridex Body Focus Side Effects (in more detail)
• Stridex Body Focus Use in Pregnancy & Breastfeeding
• Stridex Body Focus Drug Interactions
• Stridex Body Focus Support Group
• 0 Reviews for Stridex Body Focus - Add your own review/rating

Compare Stridex Body Focus with other medications

• Acne
• Dermatological Disorders

Extencilline

Extencilline may be available in the countries listed below.

Ingredient matches for Extencilline

Benzylpenicillin

Benzylpenicillin benzathine (a derivative of Benzylpenicillin) is reported as an ingredient of Extencilline in the following countries:

• France


• Russian Federation


• Tunisia

International Drug Name Search

Oralbiotico

Oralbiotico may be available in the countries listed below.

Ingredient matches for Oralbiotico

Tyrothricin

Tyrothricin is reported as an ingredient of Oralbiotico in the following countries:

• Portugal

International Drug Name Search

Apo-Nabumetone

Apo-Nabumetone may be available in the countries listed below.

Ingredient matches for Apo-Nabumetone

Nabumetone

Nabumetone is reported as an ingredient of Apo-Nabumetone in the following countries:

• Canada

International Drug Name Search

Transamin

Transamin may be available in the countries listed below.

Ingredient matches for Transamin

Tranexamic Acid

Tranexamic Acid is reported as an ingredient of Transamin in the following countries:

• Bangladesh


• Brazil


• China


• Greece


• Hong Kong


• Indonesia


• Japan


• Malaysia


• Peru


• Taiwan


• Thailand


• Vietnam

International Drug Name Search

Apomorphine Hydrochloride

Dosage Form: pellet
APOMORPHINUM MURIATICUM 3X (Apomorphine Hydrochloride) Free from yeast, wheat, corn, and soy.

DIRECTIONS: Dissolve 3 or 4 pellets

in mouth or under tongue 3 times a day or as directed by a physician.

Children 2 years and older take 1/2

adult dose.

INDICATIONS: To be used according

to standard homeopathic indications

for self limiting conditions such as

those indicated on the front panel or as directed by a physician.

Warnings: *Use only if cap and

seal are unbroken. * Keep this and all medications out of reach of children.

* If symptoms persist for more then 3

days, consult your physician.

*As with any drug, if your are pregnant or nursing a baby, seek the advice of a

health professional before using this product.*Store tightly closed in a cool, dark place.

Made according to The Homoeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768

APOMORPHINUM MURIATICUM  Apomorphine Hydrochloride  pellet

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 10191-1225 Route of Administration SUBLINGUAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Apomorphine Hydrochloride (APOMORPHINE ) Apomorphine Hydrochloride 3 [hp_X]

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 10191-1225-2 153 PELLET In 1 VIAL, GLASS None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/18/2002

Labeler - Remedy Makers (018543582)

Revised: 12/2009Remedy Makers

More Apomorphine Hydrochloride resources

• Apomorphine Hydrochloride Side Effects (in more detail)
• Apomorphine Hydrochloride Use in Pregnancy & Breastfeeding
• Apomorphine Hydrochloride Drug Interactions
• Apomorphine Hydrochloride Support Group
• 4 Reviews for Apomorphine Hydrochloride - Add your own review/rating

• Apomorphine Hydrochloride Monograph (AHFS DI)


• Apokyn Advanced Consumer (Micromedex) - Includes Dosage Information


• Apokyn MedFacts Consumer Leaflet (Wolters Kluwer)


• Apokyn Consumer Overview

Compare Apomorphine Hydrochloride with other medications

• Parkinson's Disease
• Tardive Dyskinesia

Acetazolamide Solution

Pronunciation: a-set-a-ZOLE-a-mide
Generic Name: Acetazolamide
Brand Name: Generic only. No brands available.

Acetazolamide Solution is used for:

Treating certain types of glaucoma, epilepsy, or edema (fluid buildup) in combination with other medicines. It may also be used for other conditions as determined by your doctor.

Acetazolamide Solution is a carbonic anhydrase inhibitor. It reduces fluid pressure in the eyeball by decreasing fluid formation in the eyeball. It also increases the removal of water from the body by the kidney. It also may block certain nerve discharges that may contribute to seizures.

Do NOT use Acetazolamide Solution if:

• you are allergic to any ingredient in Acetazolamide Solution


• you have adrenal gland problems, low blood levels of potassium or sodium, kidney problems, liver problems (eg, cirrhosis), high blood levels of chloride, or other electrolyte problems

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

Before using Acetazolamide Solution:

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

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


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


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


• if you have kidney stones, a lung disease, glaucoma (eg, chronic non-congestive angle-closure glaucoma), diabetes, or difficulty breathing


• if you have had a severe allergic reaction (eg, a severe rash, hives, breathing difficulties, or dizziness) to any other sulfonamide medicine such as acetazolamide, celecoxib, certain diuretics (eg, hydrochlorothiazide), glyburide, probenecid, sulfamethoxazole, valdecoxib, or zonisamide

Some MEDICINES MAY INTERACT with Acetazolamide Solution. Tell your health care provider if you are taking any of the following medicines:

• Salicylates (eg, aspirin) because they may increase the risk of Acetazolamide Solution's side effects


• Other carbonic anhydrase inhibitors (eg, methazolamide), cyclosporine, quinidine, phenytoin, amphetamine, or sodium bicarbonate because the risk of their side effects may be increased by Acetazolamide Solution


• Primidone, salicylates (eg, aspirin), lithium, or methenamine because their effectiveness may be decreased by Acetazolamide Solution

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

How to use Acetazolamide Solution:

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

• Acetazolamide Solution is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using Acetazolamide Solution at home, a health care provider will teach you how to use it. Be sure you understand how to use Acetazolamide Solution. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.


• Do not use Acetazolamide Solution if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.


• Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.


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

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

Important safety information:

• Acetazolamide Solution may cause drowsiness or temporary vision changes. These effects may be worse if you take it with alcohol or certain medicines. Use Acetazolamide Solution with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


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


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


• Diabetes patients - Acetazolamide Solution may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.


• Acetazolamide Solution may interfere with certain lab tests. Be sure your doctor and lab personnel know you are using Acetazolamide Solution.


• Lab tests, including blood electrolyte levels, complete blood cell count, or platelet levels, may be performed while you use Acetazolamide Solution. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• Use Acetazolamide Solution with caution in the ELDERLY; they may be more sensitive to its effects.


• Acetazolamide Solution should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Acetazolamide Solution while you are pregnant. It is not known if Acetazolamide Solution is found in breast milk. Do not breast-feed while using Acetazolamide Solution.

Possible side effects of Acetazolamide Solution:

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:

Blurred vision; changes in taste; constipation; diarrhea; drowsiness; frequent urination; loss of appetite; nausea; vomiting.

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); blood in urine; changes in hearing; convulsions; dark, bloody stools; dark urine; fast breathing; fever; lack of energy; lower back pain; pain, redness, or swelling at the injection site; red, swollen, or blistered skin; ringing in the ears; sore throat; tingling of the arms or legs; unusual bleeding or bruising; vision changes; yellowing of the skin or eyes.

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

See also: Acetazolamide side effects (in more detail)

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 abnormal skin sensations (eg, tingling, tickling, itching, burning); buzzing, ringing, or whistling in the ears; drowsiness; loss of appetite; loss of coordination; nausea; tremors; unsteady movements; vomiting.

Proper storage of Acetazolamide Solution:

Acetazolamide Solution is usually handled and stored by a health care provider. If you are using Acetazolamide Solution at home, store Acetazolamide Solution as directed by your pharmacist or health care provider. Keep Acetazolamide Solution out of the reach of children and away from pets.

General information:

• If you have any questions about Acetazolamide Solution, please talk with your doctor, pharmacist, or other health care provider.


• Acetazolamide Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people.


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


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

This information is summary only. It does not contain all information about Acetazolamide Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Acetazolamide resources

• Acetazolamide Side Effects (in more detail)
• Acetazolamide Use in Pregnancy & Breastfeeding
• Drug Images
• Acetazolamide Drug Interactions
• Acetazolamide Support Group
• 22 Reviews for Acetazolamide - Add your own review/rating

Compare Acetazolamide with other medications

• Edema
• Epilepsy
• Glaucoma
• Hydrocephalus
• Mountain Sickness / Altitude Sickness
• Pseudotumor Cerebri
• Seizure Prevention

Prinivil Plus

Prinivil Plus may be available in the countries listed below.

Ingredient matches for Prinivil Plus

Hydrochlorothiazide

Hydrochlorothiazide is reported as an ingredient of Prinivil Plus in the following countries:

• Spain

Lisinopril

Lisinopril dihydrate (a derivative of Lisinopril) is reported as an ingredient of Prinivil Plus in the following countries:

• Spain

International Drug Name Search

Arava

Pronunciation: le-FLOO-noe-mide
Generic Name: Leflunomide
Brand Name: Arava

Arava may cause fetal harm (eg, birth defects) or fetal death. Do not take Arava if you are pregnant or if you may become pregnant and are not using an effective form of birth control. You must make sure you are not pregnant before you start Arava. Do not become pregnant while you take Arava or for as long as any medicine remains in your body after you stop treatment. Arava may stay in the body for 2 years or longer after you stop it. Women who may become pregnant must use effective birth control while they take Arava and for as long as any medicine remains in the body.

After you stop Arava, your doctor may prescribe other medicines to help remove Arava from your body more quickly. Blood tests may also be performed to check if any medicine remains in the body. Talk with your doctor for more information and if you have questions about effective birth control.

Serious and sometimes fatal liver problems have been reported with Arava. Your doctor will monitor your liver function while you use Arava to check for liver problems. Do not take Arava if you have liver problems or if you have abnormal liver function tests before taking Arava. Ask your doctor if you are taking other medicines that may harm the liver. Contact your doctor right away if you develop symptoms of liver problems, such as dark urine, pale stools, yellowing of the skin or eyes, stomach pain, severe or persistent nausea or loss of appetite, or unusual tiredness.

Arava is used for:

Treating rheumatoid arthritis by reducing signs and symptoms, improving physical function, and preventing the development of structural damage to the joints.

Arava is a pyrimidine synthesis inhibitor. It is thought to work by blocking certain enzymes responsible for abnormal tissue development or growth.

Do NOT use Arava if:

• you are allergic to any ingredient in Arava


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


• you may become pregnant and are not using effective birth control


• you have bone marrow problems; a severely weakened immune system; or a severe, uncontrolled infection


• you have liver problems (eg, hepatic insufficiency or failure), abnormal liver function tests prior to taking Arava, or a history of hepatitis B or C infection

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

Before using Arava:

Some medical conditions may interact with Arava. 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 a weakened immune system, an infection, a history of an infection that keeps coming back, or you have recently received a vaccination


• if you have a history of lung problems, tuberculosis (TB) or a positive TB test, high blood pressure, blood or bone marrow problems, diabetes, liver problems, abnormal liver function tests, or if you drink alcoholic beverages


• if you have or have a history of kidney problems or you are on dialysis


• if you take or have recently taken methotrexate, another medicine to treat rheumatoid arthritis, or another medicine that may suppress your immune system


• if you are taking medicine to treat or prevent malaria

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

• Methotrexate because the risk of liver problems, blood problems, or infection may be increased


• Rifampin because it may increase the risk of Arava's side effects


• Anticoagulants (eg, warfarin) because the risk of its side effects, including bleeding, may be increased by Arava


• Medicines that may suppress the immune system because the risk of infection or unusual bruising or bleeding may be increased. Ask your doctor if you are unsure if any of your medicines may suppress the immune system


• Medicines that may cause nerve problems, because the risk of a certain nerve side effect (burning, numbness, or tingling sensation) may be increased. Ask your doctor if you are unsure if any of you medicines may cause nerve problems


• Cholestyramine because it may decrease Arava's effectiveness


• Medicines that may harm the liver (eg, acetaminophen, methotrexate, ketoconazole, isoniazid, certain medicines for HIV infection) because the risk of liver side effects may be increased. Ask your doctor if you are unsure if any of your medicines might harm the liver

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

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

• Take Arava by mouth with or without food.


• It may take 4 weeks or more to notice any improvement while taking Arava.


• If you miss a dose of Arava, 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 Arava.

Important safety information:

• Arava may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Arava with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Drinking alcohol while you are taking Arava may increase the risk of liver problems. Talk with your doctor before drinking alcohol while taking Arava.


• Arava may reduce the number of clot-forming cells (platelets) in your blood. Avoid activities that may cause bruising or injury. Tell your doctor if you have unusual bruising or bleeding. Tell your doctor if you have dark, tarry, or bloody stools.


• Arava may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.


• Do not receive a live vaccine (eg, measles, mumps) while you are taking Arava. Talk with your doctor before you receive any vaccine.


• The safety of Arava in patients with inactive TB has not been confirmed. You may need to have a TB skin test before you start Arava to determine if you have TB infection. Discuss any questions or concerns with your doctor.


• Serious and sometimes fatal liver problems have been reported with Arava. Contact your doctor right away if you develop symptoms such as dark urine, pale stools, yellowing of the skin or eyes, stomach pain, severe or persistent nausea or loss of appetite, or unusual tiredness.


• A serious and sometimes fatal lung problem (interstitial lung disease) has been reported with Arava. Contact your doctor right away if you develop new or worsening breathing problems, such as cough or shortness of breath (with or without fever).


• Serious and sometimes fatal skin reactions (eg, Stevens-Johnson syndrome, toxic epidermal necrolysis) have been rarely reported with Arava. Contact your doctor right away if you develop a rash; red, swollen, blistered, or peeling skin; or blisters on the inside of the eyes, nose, or mouth.


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


• Use Arava with caution in the ELDERLY; they may be more likely to develop burning, numbness, or tingling.


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


• Arava may remain in the body for 2 years or longer after you stop taking it. Your doctor may prescribe medicine to help remove Arava from your body more quickly after you finish treatment (drug elimination procedure). Talk with your doctor for more information.


• The risk of harm or death to a fetus fathered by a man using Arava is not known. Men who take Arava should talk with their doctor about the need to use a condom when having sex with a woman who may become pregnant. If you wish to father a child, talk with your doctor. You may need to stop Arava and complete the drug elimination procedure to remove it from your blood before you father a child.


• If you are able to become pregnant, you must not start Arava unless it has been confirmed that you are not pregnant. You will need to use an effective form of birth control while you take Arava and for as long as Arava remains in your body. If you plan to become pregnant, talk with your doctor about stopping Arava and completing the drug elimination procedure before you become pregnant. Talk with your doctor for more information or if you have questions about effective birth control.


• PREGNANCY and BREAST-FEEDING: Do not use Arava if you are pregnant. It may cause birth defects or fetal death. You must have a negative pregnancy test before you start treatment with Arava. Do not become pregnant while you are taking it. Contact your doctor at once if your period does not occur when expected or if you suspect that you are pregnant. It is not known if Arava is found in breast milk. Do not breast-feed while taking Arava.

Possible side effects of Arava:

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:

Back pain; diarrhea; dizziness; hair loss; headache; indigestion; muscle aches; nausea; runny nose; weakness; weight loss.

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); blisters on the inside of the eyes, nose, or mouth; burning, numbness, or tingling; chest pain; fast or irregular heartbeat; muscle cramps, including leg cramps; new or worsening breathing problems (eg, cough or shortness of breath, with or without fever); red, swollen, blistered, or peeling skin; severe or persistent vomiting; symptoms of high blood pressure (eg, severe or persistent headache or dizziness, vision changes); symptoms of infection (eg, fever, chills, sore throat, cough, increased or painful urination); symptoms of liver problems (eg, dark urine, pale stools, yellowing of the skin or eyes, stomach pain, severe or persistent nausea or loss of appetite); unusual or easy bruising or bleeding; unusual tiredness; unusually pale skin.

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.

See also: Arava side effects (in more detail)

If OVERDOSE is suspected:

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

Proper storage of Arava:

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

General information:

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


• Arava 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 is a summary only. It does not contain all information about Arava. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Arava resources

• Arava Side Effects (in more detail)
• Arava Use in Pregnancy & Breastfeeding
• Drug Images
• Arava Drug Interactions
• Arava Support Group
• 10 Reviews for Arava - Add your own review/rating

• Arava Prescribing Information (FDA)


• Arava Advanced Consumer (Micromedex) - Includes Dosage Information


• Arava Concise Consumer Information (Cerner Multum)


• Arava Monograph (AHFS DI)


• Leflunomide Prescribing Information (FDA)


• Leflunomide Professional Patient Advice (Wolters Kluwer)

Compare Arava with other medications

• Rheumatoid Arthritis

Aromasin

Pronunciation: EX-e-MES-tane
Generic Name: Exemestane
Brand Name: Aromasin

Aromasin is used for:

Treating advanced breast cancer in women who are past menopause and whose disease has progressed after treatment with other medicines. It is also used in the treatment of early breast cancer in certain women who are past menopause and after treatment with other medicines. It may also be used for other conditions as determined by your doctor.

Aromasin is an aromatase inhibitor. It works by stopping the production of estrogen, which may decrease the size and growth of the tumor.

Do NOT use Aromasin if:

• you are allergic to any ingredient in Aromasin


• you have not undergone menopause


• you are pregnant, may become pregnant, or are breast-feeding


• you are taking any medicines that contain estrogen (eg, certain birth control pills, certain hormone replacement therapies)

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

Before using Aromasin:

Some medical conditions may interact with Aromasin. 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 a history of liver or kidney problems, osteoporosis (weak bones), heart problems, blood vessel problems, or a stroke

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

• Carbamazepine, medicines that contain estrogen (eg, certain birth control pills, certain hormone replacement therapies), phenobarbital, phenytoin, rifampin, or St. John's wort because they may decrease Aromasin's effectiveness

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

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

• An extra patient leaflet is available with Aromasin. Talk to your pharmacist if you have questions about this information.


• Take Aromasin by mouth after a meal at the same time every day.


• Continue to take Aromasin even if you feel well. Do not miss any doses.


• If you miss a dose of Aromasin, 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 Aromasin.

Important safety information:

• Aromasin may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Aromasin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• It may take several weeks for Aromasin to work. Do not stop taking Aromasin or take Aromasin for longer than prescribed without checking with your doctor.


• Lab tests, including complete blood cell counts, liver and kidney function, or bone density, may be performed while you take Aromasin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• Aromasin should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: Do not take Aromasin if you are pregnant. It has been shown to cause harm to the fetus. Avoid becoming pregnant while you are taking it. If you may become pregnant, you must use effective birth control while you take Aromasin. Talk with your doctor about the use of effective birth control while you take Aromasin. If you think you may be pregnant, contact your doctor right away. It is not known if Aromasin is found in breast milk. Do not breast-feed while taking Aromasin.

Possible side effects of Aromasin:

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:

Anxiety; back, joint, muscle, or limb pain; constipation; coughing; diarrhea; dizziness; flu-like symptoms; hair loss; headache; hot flashes; increased or decreased appetite; increased sweating; nausea; stomach pain or upset; tiredness; trouble sleeping; weight gain; vomiting.

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); chest pain; confusion; depression; fainting; general feeling of being unwell; numbness, burning, or tingling in the skin, hands, or feet; numbness of an arm or leg; one-sided weakness; severe or sudden bone pain; severe stomach pain; shortness of breath; sudden, severe dizziness, headache, or vomiting; sudden, unusual weight gain; swelling of the hands, legs, or feet; vision or speech changes; yellowing of the skin or eyes.

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

See also: Aromasin side effects (in more detail)

If OVERDOSE is suspected:

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

Proper storage of Aromasin:

Store Aromasin at 77 degrees F (25 degrees C) in a tightly closed container. Brief storage at temperatures 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 Aromasin out of the reach of children and away from pets.

General information:

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


• Aromasin 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 is a summary only. It does not contain all information about Aromasin. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Aromasin resources

• Aromasin Side Effects (in more detail)
• Aromasin Use in Pregnancy & Breastfeeding
• Drug Images
• Aromasin Drug Interactions
• Aromasin Support Group
• 7 Reviews for Aromasin - Add your own review/rating

• Aromasin Prescribing Information (FDA)


• Aromasin Consumer Overview


• Aromasin Monograph (AHFS DI)


• Aromasin Advanced Consumer (Micromedex) - Includes Dosage Information


• Exemestane Professional Patient Advice (Wolters Kluwer)

Compare Aromasin with other medications

• Breast Cancer

Cefixime

Pronunciation: sef-IX-eem
Generic Name: Cefixime
Brand Name: Suprax

Cefixime is used for:

Treating infections caused by certain bacteria.

Cefixime is a cephalosporin antibiotic. It works by killing sensitive bacteria.

Do NOT use Cefixime if:

• you are allergic to any ingredient in Cefixime or to other cephalosporins (eg, cephalexin)


• you will be having a live typhoid vaccine

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

Before using Cefixime:

Some medical conditions may interact with Cefixime. 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 had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin (eg, amoxicillin) or beta-lactam antibiotic (eg, imipenem)


• if you have diarrhea, stomach or bowel problems (eg, inflammation), bleeding or blood clotting problems, liver problems, or poor nutrition


• if you have a history of kidney problems or you are on dialysis treatment

Some MEDICINES MAY INTERACT with Cefixime. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• Anticoagulants (eg, warfarin) or carbamazepine because the risk of their side effects may be increased by Cefixime


• Live typhoid vaccines because their effectiveness may be decreased by Cefixime

Ask your health care provider if Cefixime 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 Cefixime:

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

• Take Cefixime by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.


• To clear up your infection completely, continue using Cefixime for the full course of treatment even if you feel better in a few days.


• If you miss a dose of Cefixime, 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 Cefixime.

Important safety information:

• Cefixime may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Cefixime with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Do not change dose forms (eg, tablets, suspension) of Cefixime without talking with your doctor.


• Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using 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.


• Cefixime only works against bacteria; it does not treat viral infections (eg, the common cold).


• Be sure to use Cefixime 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.


• Long-term or repeated use of Cefixime 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.


• Cefixime may reduce the number of clot-forming cells (platelets) in your blood. Avoid activities that may cause bruising or injury. Tell your doctor if you have unusual bruising or bleeding. Tell your doctor if you have dark, tarry, or bloody stools.


• Do not receive a live typhoid vaccine while you are taking Cefixime. It may not work as well. Talk with your doctor if you are scheduled to receive a live typhoid vaccine.


• Diabetes patients - Cefixime may cause the results of some tests for urine glucose or urine ketones to be wrong. Ask your doctor before you change your diet or the dose of your diabetes medicine.


• Cefixime may interfere with certain lab tests. Be sure your doctor and lab personnel know you are using Cefixime.


• Cefixime should be used with extreme caution in CHILDREN younger than 6 months old; safety and effectiveness in these children have not been confirmed.


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

Possible side effects of Cefixime:

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:

Diarrhea; gas; loose stools; nausea; stomach pain or upset.

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; unusual hoarseness); bloody stools; decreased urination; fever, chills, or sore throat; red, swollen, blistered, or peeling skin; seizures; severe diarrhea; severe nausea or vomiting; severe stomach pain or cramping; unusual bruising or bleeding; vaginal discharge or itching; white spots in the mouth; yellowing of the skin or eyes.

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

See also: Cefixime side effects (in more detail)

If OVERDOSE is suspected:

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

Proper storage of Cefixime:

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

General information:

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


• Cefixime 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 is a summary only. It does not contain all information about Cefixime. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Cefixime resources

• Cefixime Side Effects (in more detail)
• Cefixime Dosage
• Cefixime Use in Pregnancy & Breastfeeding
• Cefixime Drug Interactions
• Cefixime Support Group
• 2 Reviews for Cefixime - Add your own review/rating

• Cefixime Monograph (AHFS DI)


• Cefixime Professional Patient Advice (Wolters Kluwer)


• cefixime Concise Consumer Information (Cerner Multum)


• cefixime Advanced Consumer (Micromedex) - Includes Dosage Information


• Suprax Prescribing Information (FDA)

Compare Cefixime with other medications

• Bladder Infection
• Bronchitis
• Gonococcal Infection, Disseminated
• Gonococcal Infection, Uncomplicated
• Kidney Infections
• Otitis Media
• Pneumonia
• Sinusitis
• STD Prophylaxis
• Tonsillitis/Pharyngitis
• Upper Respiratory Tract Infection
• Urinary Tract Infection

Artificial Saliva Spray

Generic Name: Artificial Saliva
Brand Name: Salivart

Artificial Saliva Spray is used for:

Relieving dry mouth and throat.

Artificial Saliva Spray is an artificial saliva. It works by moistening and lubricating the mouth and throat.

Do NOT use Artificial Saliva Spray if:

• you are allergic to any ingredient in Artificial Saliva Spray

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

Before using Artificial Saliva Spray:

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

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


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


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

Some MEDICINES MAY INTERACT with Artificial Saliva Spray. However, no specific interactions with Artificial Saliva Spray are known at this time.

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

Use Artificial Saliva Spray as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Spray 1 or 2 times into the mouth whenever it feels uncomfortably dry.


• If you miss taking a dose of Artificial Saliva Spray for 1 or more days, there is no cause for concern. If your doctor recommended that you take it, try to remember your dose every day.

Ask your health care provider any questions you may have about how to use Artificial Saliva Spray.

Important safety information:

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

Possible side effects of Artificial Saliva Spray:

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

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

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

If OVERDOSE is suspected:

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

Proper storage of Artificial Saliva Spray:

Store Artificial Saliva Spray at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not refrigerate. Store away from heat, moisture, and light. Do not store in the bathroom. Store away from heat and direct sunlight. Do not puncture, break, or burn the canister even if it appears to be empty. Keep Artificial Saliva Spray out of the reach of children and away from pets.

General information:

• If you have any questions about Artificial Saliva Spray, please talk with your doctor, pharmacist, or other health care provider.


• Artificial Saliva Spray 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 is a summary only. It does not contain all information about Artificial Saliva Spray. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Artificial Saliva resources

• Artificial Saliva Use in Pregnancy & Breastfeeding
• Artificial Saliva Support Group
• 2 Reviews for Artificial Saliva - Add your own review/rating

Compare Artificial Saliva with other medications

• Mucositis
• Xerostomia

C-Tri

C-Tri may be available in the countries listed below.

Ingredient matches for C-Tri

Ceftriaxone

Ceftriaxone is reported as an ingredient of C-Tri in the following countries:

• Myanmar

International Drug Name Search

Mymox

Mymox may be available in the countries listed below.

Ingredient matches for Mymox

Amoxicillin

Amoxicillin is reported as an ingredient of Mymox in the following countries:

• Latvia

Amoxicillin trihydrate (a derivative of Amoxicillin) is reported as an ingredient of Mymox in the following countries:

• Sri Lanka

International Drug Name Search

Tevapirin

Tevapirin may be available in the countries listed below.

Ingredient matches for Tevapirin

Aspirin

Acetylsalicylic Acid is reported as an ingredient of Tevapirin in the following countries:

• Israel

International Drug Name Search

Anastrozol Mepha

Anastrozol Mepha may be available in the countries listed below.

Ingredient matches for Anastrozol Mepha

Anastrozole

Anastrozole is reported as an ingredient of Anastrozol Mepha in the following countries:

• Switzerland

International Drug Name Search

Allfen

Pronunciation: gwye-FEN-eh-sin/poe-TASS-ee-um gwye-a-kole-SUL-foe-nate
Generic Name: Guaifenesin/Potassium Guaiacolsulfonate
Brand Name: Allfen and Humibid LA

Allfen is used for:

Relieving symptoms of cough and mucus in the chest due to respiratory infections, asthma, colds, or hay fever. It may also be used for other conditions as determined by your doctor.

Allfen is a combination of 2 expectorants. It works by thinning mucus (phlegm) in the lungs and making it less sticky and easier to cough up. This reduces chest congestion by making coughs more productive.

Do NOT use Allfen if:

• you are allergic to any ingredient in Allfen

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

Before using Allfen:

Some medical conditions may interact with Allfen. 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 a chronic cough that occurs with smoking, asthma, chronic bronchitis, or emphysema, or if cough occurs with large amounts of mucus

Some MEDICINES MAY INTERACT with Allfen. Tell your health care provider if you are taking any other medicines. However, no specific interactions with Allfen are known at this time.

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

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

• Allfen may be taken with or without food.


• Drinking extra fluids while you are taking Allfen is recommended. Check with your doctor for instructions.


• Swallow Allfen whole. Do not break, crush, or chew before swallowing.


• If you miss a dose of Allfen and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose 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 Allfen.

Important safety information:

• Allfen may cause dizziness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Allfen. Using Allfen alone, with certain other medicines, or with alcohol may lessen your ability to drive or to perform other potentially dangerous tasks.


• If cough persists for more than 1 week or is accompanied by a fever, contact your health care provider. A persistent cough could be a sign of a serious condition.


• Allfen may interfere with some lab tests. Make sure your doctor and lab personnel know you are taking Allfen.


• Use Allfen with extreme caution in CHILDREN younger than 12 years of age. Safety and effectiveness in this age group have not been confirmed.


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

Possible side effects of Allfen:

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:

Dizziness; headache; nausea; upset stomach; vomiting.

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

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

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. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch .

See also: Allfen side effects (in more detail)

If OVERDOSE is suspected:

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

Proper storage of Allfen:

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

General information:

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


• Allfen 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 is a summary only. It does not contain all information about Allfen. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Allfen resources

• Allfen Side Effects (in more detail)
• Allfen Use in Pregnancy & Breastfeeding
• Allfen Drug Interactions
• Allfen Support Group
• 0 Reviews for Allfen - Add your own review/rating

• Allfen Advanced Consumer (Micromedex) - Includes Dosage Information


• Guaifenesin Monograph (AHFS DI)


• Guaifenesin NR Prescribing Information (FDA)


• Mucinex Prescribing Information (FDA)


• Mucinex Consumer Overview


• Organidin NR Prescribing Information (FDA)


• Tussin Consumer Overview

Compare Allfen with other medications

• Cough

Apexicon Cream

Pronunciation: dye-FLOR-a-sone die-ASS-eh-tate
Generic Name: Diflorasone Diacetate
Brand Name: Examples include Apexicon and Maxiflor

Apexicon Cream is used for:

Treating inflammation and itching due to certain skin conditions.

Apexicon Cream is a topical corticosteroid. It works by reducing skin inflammation (redness, swelling, itching, and irritation).

Do NOT use Apexicon Cream if:

• you are allergic to any ingredient in Apexicon Cream

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

Before using Apexicon Cream:

Some medical conditions may interact with Apexicon Cream. 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 an acne-like rash, measles, inflammation of the skin around the mouth, thinning skin, skin infection, or chickenpox


• if you have tuberculosis or have had a positive tuberculin skin test, or if you have recently had a vaccination

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

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

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

• Apply a small amount of medicine to the affected area. Gently rub the medicine in until it is evenly distributed.


• Wash your hands after applying Apexicon Cream unless your hands are part of the treated area.


• Do not bandage or wrap the affected area unless directed otherwise by your doctor.


• If you miss a dose of Apexicon Cream, apply 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.

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

Important safety information:

• Apexicon Cream is for external use only. Avoid contact with the eyes.


• Contact your health care provider if any side effects occur, especially under an occlusive dressing.


• Do not use Apexicon Cream for longer than the time prescribed. Overuse of topical products may worsen your condition or increase your risk for side effects.


• Do not use Apexicon Cream for other skin conditions at a later time.


• If Apexicon Cream is prescribed to treat the diaper area, avoid using tight-fitting diapers or plastic pants.


• Check with your doctor before having vaccinations while using Apexicon Cream.


• Use Apexicon Cream with extreme caution in CHILDREN. Safety and effectiveness have not been confirmed.


• In some instances, corticosteroid medicines may affect the growth rate in CHILDREN and adolescents. Your child's growth may need to be checked regularly while he or she is using Apexicon Cream.


• PREGNANCY and BREAST-FEEDING: If you plan on becoming pregnant, discuss with your doctor the benefits and risks of using Apexicon Cream during pregnancy. It is unknown if Apexicon Cream is excreted in breast milk. If you are or will be breast-feeding while you are using Apexicon Cream, check with your doctor or pharmacist to discuss the risks to your baby.

Possible side effects of Apexicon Cream:

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:

Dryness; itching.

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

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); acne-like rash; burning, cracking, irritation, itching, or peeling not present before you began using Apexicon Cream; excessive hair growth; inflamed hair follicles; inflammation around the mouth; muscle weakness; thinning, softening, or discoloration of the skin; unusual weight gain, especially in the face.

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.

See also: Apexicon side effects (in more detail)

If OVERDOSE is suspected:

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

Proper storage of Apexicon Cream:

Store Apexicon Cream at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Apexicon Cream out of the reach of children and away from pets.

General information:

• If you have any questions about Apexicon Cream, please talk with your doctor, pharmacist, or other health care provider.


• Apexicon Cream 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 is a summary only. It does not contain all information about Apexicon Cream. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Apexicon resources

• Apexicon Side Effects (in more detail)
• Apexicon Use in Pregnancy & Breastfeeding
• Apexicon Drug Interactions
• Apexicon Support Group
• 0 Reviews for Apexicon - Add your own review/rating

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