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  • JERUSALEM, Israel----Dec. 7, 2005--Teva Pharmaceutical Industries Ltd. announced today that the U.S. Food and Drug Administration has granted final approval for the Company's ANDA for Oxycodone Extended Release Tablets, 10 mg, 20 mg and 40 mg.
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  • U.S. drug manufacturers, distributors, and pharmacy benefit managers (PBMs) are adapting to a political and consumer environment attempting to control drug spending in order to contain rising overall health care costs.
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  • Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA) announced today that the U.S. Food and Drug Administration has granted final approval for the Company's ANDA for Ribavirin Tablets, 200 mg. Shipment of this product will begin immediately.
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  • French drug giant Sanofi Aventis said Friday that federal regulators have agreed to speed up the review process for the company's application to sell a new chemotherapy treatment for advanced stomach cancer.
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  • Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA) issued the following statement regarding the outstanding 1.5% Convertible Senior Notes due 2025 of Ivax Corporation, in connection with Teva's pending acquisition of Ivax.
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  • JERUSALEM----Dec. 5, 2005--Teva Pharmaceutical Industries Ltd. announced today that the U.S. Food and Drug Administration has granted final approval for the Company's ANDA for Ribavirin Tablets, 200 mg.
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  • PORT TOWNSEND -- Jessica Coggins is used to helping others rather than asking for help. As a student of alternative medicine, she has traveled around the world learning about healing and the arts, and completed a degree in expressive healing from Western Washington University.
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  • BOCA RATON — Osmotica Pharmaceutical, a specialty drug company in Boca Raton, has received approval to market its first drug in the United States.
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  • The Federal Trade Commission has notified Teva Pharmaceutical Industries Ltd.
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  • JERUSALEM----Dec. 2, 2005--The Federal Trade Commission has notified Teva Pharmaceutical Industries Ltd. and Wyeth that it will not file an objection with the United States District Court for the District of New Jersey to the proposed settlement of the patent litigation between Teva and Wyeth concerning Teva's application to market an extended release venlafaxine capsule product.
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Terms


ALLEGRA

Drug Uses

Allegra is indicated for the relief of symptoms associated with seasonal allergic rhinitis in adults and children 6 years of age and older. Symptoms treated effectively were sneezing, rhinorrhea, itchy nose/palate/throat, itchy/watery/red eyes.

How Taken

Allegra is formulated as a capsule or tablet for oral administration. Allegra is usually taken twice a day, in the morning and the evening. Follow your doctor\'s instructions. Take each dose with a full glass of water.

Warnings/Precautions

Do not take Allegra if you have ever had an allergic reaction to it. Before taking this medication, tell your doctor if you have any serious illness such as heart, kidney, or liver disease. You may require a dosage adjustment or special monitoring during treatment if you have other illnesses. Allegra is in the FDA pregnancy category C. This means that it is not known whether Allegra will harm an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant. It is also not known whether Allegra passes into breast milk. Do not take Allegra without first talking to your doctor if you are breast-feeding a baby. Allegra is not approved for use by children younger than 6 years of age.

Missed Dose

If you miss a dose, use 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-up" the dose to catch up.

Possible Side Effects

Stop taking Allegra and seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives). Allergic reactions occur only rarely, and other serious side effects are not likely to occur. Some less serious side effects may be more likely to occur. Continue to take Allegra and talk to your doctor if you experience nausea or an upset stomach. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Storage

Store Allegra capsules and tablets at controlled room temperature 20-25°C (68-77°F). Foil-backed blister packs containing Allegra capsules and all tablet packaging should be protected from excessive moisture.

Overdose

Symptoms and signs of Allegra overdose are: dizziness, drowsiness, and dry mouth. Seek emergency medical attention.

More Information

Tell your doctor of all nonprescription and prescription medication you may use, especially: MAO inhibitors, certain blood pressure drugs, digoxin, and all adrenaline-like drugs. Report other drugs which affect the heart rhythm. Ask your doctor or pharmacist for more details. Check the labels carefully on all nonprescription products, such as cough-and-cold medicines that contain antihistamines and decongestants. Consult your pharmacist. Do not take Allegra for several days before any allergy testing since test results can be affected. Do not start or stop any medicine without doctor or pharmacist approval.

Disclaimer

This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.