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Combivir is a prescription medication used to treat human immunodeficiency virus (HIV) infection. Combivir is also used to treat chronic hepatitis B virus infection. Combivir belongs to a group of drugs called nucleoside reverse transcriptase inhibitors (NRTI), which block a process HIV and hepatitis B viruses need to reproduce.
This medication comes in tablet and oral liquid forms and is taken once or twice a day, depending on the condition being treated.
Combivir can be taken with or without food.
Some of the common side effects of lamivudine include ear, nose or throat infections, diarrhea, headache, ill feeling, and fatigue.
Combivir is a prescription medicine used to treat human immunodeficiency virus (HIV) infection and chronic hepatitis B infection virus infection in adults and children.
Combivir is not cure for HIV infection or hepatitis B infection virus infection.
This medication may be prescribed for other uses. Ask your doctor or pharmacist for more information.
Combivir may be found in some form under the following brand names:
Combivir is part of the drug class:
Serious side effects can occur with lamivudine use. See “Combivir Precautions” section.
Commonly reported side effects include:
This is not a complete list of lamivudine side effects. Ask your doctor or pharmacist for more information.
Tell your doctor about all the medicines you take including prescription and non-prescription medicines, vitamins, and herbal supplements. Especially tell your doctor if you take:
Ask your doctor if you are unsure if you are taking any of these medications.
This is not a complete list of lamivudine drug interactions. Ask your doctor or pharmacist for more information.
Incidence, characteristics and clinical impact of lamivudine resistance in chronic hepatitis B, J Hepatol, 1998, vol. 28 pg. 48 Google Scholar Crossref Search ADS 14 Cane PA, Cook P, Ratcliffe D, Mutimer D, Pillay D.It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide.
Changes in fat mitochondrial DNA and function in subjects randomized to abacavir-lamivudine or tenofovir DF-emtricitabine with atazanavir-ritonavir or efavirenz: AIDS Clinical Trials Group study A5224s, substudy of A5202. Hepatic impairment does not affect the pharmacokinetics of lamivudine. Participants were randomly assigned (1:1), via a computer-generated allocation sequence (block size of four), to receive coformulated bictegravir 50 mg, emtricitabine 200 mg, and tenofovir alafenamide 25 mg or coformulated dolutegravir 50 mg, abacavir 600 mg, and lamivudine 300 mg, with matching placebo, once daily for 144 weeks.
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