Combivir Generic Name & Formulations
Legal Class
Rx
General Description
Lamivudine 150mg, zidovudine 300mg; scored tabs.
Pharmacological Class
Nucleoside analogues (reverse transcriptase inhibitors).
How Supplied
Tabs—60
Manufacturer
Combivir Indications
Indications
HIV-1 infection, in combination with other antiretroviral agents.
Combivir Dosage and Administration
Adults and Children
<30kg: not recommended. ≥30kg: 1 tab twice daily. Hepatic or renal impairment (CrCl <50mL/min): not recommended; use individual components.
Combivir Contraindications
Not Applicable
Combivir Boxed Warnings
Boxed Warning
Hematologic toxicity. Myopathy. Lactic acidosis and severe hepatomegaly with steatosis. Exacerbations of hepatitis B.
Combivir Warnings/Precautions
Warnings/Precautions
Risk of hematologic toxicity/bone marrow suppression; monitor CBCs esp. in advanced HIV-1 disease; interrupt dose if anemia or neutropenia occurs. Myopathy with prolonged zidovudine use. Suspend if lactic acidosis or pronounced hepatotoxicity (eg, hepatomegaly, steatosis) occurs. Not for treating chronic HBV infection; closely monitor patients co-infected with HBV and HIV for several months after stopping treatment (discontinuing therapy may exacerbate HBV infection); if appropriate, initiate anti-hepatitis B therapy may be warranted. History of pancreatitis. Monitor for lipoatrophy; use alternatives if suspected. Women. Obesity. Elderly. Pregnancy. Nursing mothers: not recommended.
Combivir Pharmacokinetics
See Literature
Combivir Interactions
Interactions
Avoid concomitant stavudine, doxorubicin, nucleoside analogues (eg, ribavirin), sorbitol-containing products. Increased hematologic toxicity with ganciclovir, interferon alpha, ribavirin, other bone marrow suppressants or cytotoxic drugs. Monitor for treatment-associated toxicities (eg, hepatic decompensation) with interferon-alpha with or without ribavirin.
Combivir Adverse Reactions
Adverse Reactions
Headache, nausea, malaise, fatigue, nasal symptoms, diarrhea, cough; neutropenia, anemia, lactic acidosis, severe hepatomegaly with steatosis, myopathy, myositis, immune reconstitution syndrome, pancreatitis (discontinue if occurs), lipoatrophy.
Combivir Clinical Trials
See Literature
Combivir Note
Notes
Register pregnant patients exposed to lamivudine by calling (800) 258-4263.
Combivir Patient Counseling
See Literature