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Studies Tout Alternative HIV Regimens for Women, Babies - BusinessWeek
MD News (press release)Studies Tout Alternative HIV Regimens for Women, BabiesBusinessWeekThe regimens were nevirapine plus tenofovir-emtricitabine or ritonavir-boosted lopinavir plus tenofovir-emtricitabine. In the other study, ...Nevirapine May Not Always Be Best Choice for Peripartum Antiretroviral TreatmentMedscapePreventive HIV Therapy May Limit Later ResponseMedPage TodayLopinavir-based regimen may be superior to nevirapine-based regimen for some ...Pediatric SuperSiteMD News (press release)all 28 news articles��
Viread(R) for Hepatitis B Maintains Antiviral Suppression with No Development ... - MarketWatch (press release)
Viread(R) for Hepatitis B Maintains Antiviral Suppression with No Development ...MarketWatch (press release)After 72 weeks, patients with confirmed viremia (HBV DNA levels at or above 400 copies/mL on two consecutive visits) had the option of adding emtricitabine ...and more��
Gilead Sciences Announces Third Quarter 2010 Financial Results - MarketWatch (press release)
Gilead Sciences Announces Third Quarter 2010 Financial ResultsMarketWatch (press release)Sales of Atripla(R) (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil fumarate 300 mg) for the treatment of HIV infection increased 23 percent ...and more��
Owing Largely to the Generic Erosion of Key Antiretroviral Agents, Growth in ... - PR Newswire (press release)
Owing Largely to the Generic Erosion of Key Antiretroviral Agents, Growth in ...PR Newswire (press release)"Assuming concerns over rilpivirine's virological failure rate are resolved, the coformulation of rilpivirine/tenofovir/emtricitabine has the potential to ...and more��
Last updated on: Jan 24, 2007
Brand Name: | Emtriva |
Active Ingredient: | emtricitabine |
Strength(s): | 200 mg |
Dosage Form(s): | Capsule |
Company Name: | Gilead Sciences |
Availability: | Prescription only |
*Date Approved by the FDA: | July 2, 2003 |
*Approval by FDA does not mean that the drug is available to consumers at this time.
This information is provided by the U.S. Food & Drug Administration.
For more information about this drug, click here. |
Emtriva is a type of medicine called an HIV (human immunodeficiency virus) nucleoside reverse transcriptase inhibitor (NRTI). Emtriva helps to block HIV reverse transcriptase, a chemical in your body (enzyme) that is needed for HIV to multiply. Emtriva is always used with other anti-HIV medicines to treat people with HIV infection. Emtriva is for adults age 18 and older. Emtriva has not been studied fully in children under age 18 or adults over age 65.
Emtriva does not cure HIV infection or AIDS. The long-term effects of Emtriva are not known at this time. Emtriva may lower the amount of HIV in the blood (viral load). Emtriva may also help to increase the number of T cells called CD4 cells. Lowering the amount of HIV in the blood lowers the chance of death or infections that happen when your immune system is weak (opportunistic infections). People taking Emtriva may still get opportunistic infections or other conditions that happen with HIV infection.
Emtriva does not lower your chances of passing HIV to other people through sexual contact, sharing needles, or being exposed to blood. For your health and the health of others, it is important to always practice safe sex and never use or share dirty needles.
It is very important that you see your healthcare provider regularly while taking Emtriva.
Who should not take Emtriva?
Do not take Emtriva if you are allergic to Emtriva or any of its ingredients.
Special Warnings:
General Precautions with Emtriva:
What should I tell my health care provider?
Tell your health care provider:
What are some possible side effects of Emtriva? (This is NOT a complete list of side effects reported with Emtriva. Your health care provider or pharmacist can discuss with you a more complete list of side effects.)
Serious side effects with Emtriva include:
Some common side effects with Emtriva include:
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