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Substance

Lamivudine / zidovudine

Brand name:
Combivir

Description

 
Hiv antiviral
 
The combination of these two components significantly reduces the risk of disease progression and the likelihood of death
Brands:
Combivir
Availability:
Prescription needed
Pregnancy:
Consult a doctor
Alcohol:
Not detected with light alcohol consumption
Side Effects:
Pale skin
Interactions:
Alprazolam
For informational purposes only. Consult your local medical authority for advice.

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Combivir is used to treat HIV, the virus that can cause acquired immunodeficiency syndrome (AIDS). Combivir does not contain gluten Combivir is a combination drug that pairs azidothymidine, also known as AZT, with another antiviral, lamivudine. It has annual US sales of around 5 million, according to IMS data Brand name: Combivir Generic name: lamivudine/zidovudine, or 3TC/AZT Class: Nucleoside reverse transcriptase inhibitor (nucleoside, NRTI, or nuke) -- fixed dose combination Manufacturer: ViiV Healt. Lamivudine/Zidovudine is available only in 60 count bottle PITTSBURGH, Oct. Combivir is a nucleoside reverse transcriptase inhibitor (NRTI) that is used in conjunction with other ARVs to treat HIV disease /PRNewswire/ -- Mylan Inc. Launch of its Lamivudine and Zidovudine Tablets USP, 150 mg/300 mg, which is the generic version of. Food and Drug Administration (FDA) has approved a generic version of the antiretroviral (ARV) Combivir (zidovudine plus lamivudine) for sale in the United States. Launch of its Lamivudine and Zidovudine Tablets USP, 150 mg/300 mg, which is the generic Mylan Launches Generic Combivir®. Combivir contains two active substances, lamivudine and zidovudine. Combivir contains a combination of lamivudine and zidovudine. 3, 2014 /PRNewswire/ -- Mylan Inc. It has annual US sales of around 5 million, according to IMS data Combivir (lamivudine / zidovudine) Descovy (emtricitabine / tenofovir alafenamide) Bictegravir / emtricitabine / tenofovir alafenamide Prescription only Prescribed for HIV Infection, Nonoccupational Exposure, Occupational Exposure. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. 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