Abacavir/lamivudine/zidovudine
Combination of | |
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Abacavir sulfate | Nucleoside analogue reverse transcriptase inhibitor |
Lamivudine | Nucleoside analogue reverse transcriptase inhibitor |
Zidovudine | Nucleoside analogue reverse transcriptase inhibitor |
Clinical data | |
Trade names | Trizivir |
AHFS/Drugs.com | Professional Drug Facts |
MedlinePlus | a616051 |
License data | |
Pregnancy category |
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Routes of administration | By mouth |
ATC code | |
Legal status | |
Legal status | |
Identifiers | |
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PubChem CID | |
ChemSpider | |
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NIAID ChemDB | |
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Abacavir/lamivudine/zidovudine, sold under the brand name Trizivir, is a fixed-dose combination antiretroviral medication for the treatment of HIV/AIDS.[2][3][4] It contains three reverse transcriptase inhibitors patented by GlaxoSmithKline and marketed by a joint venture with Pfizer, ViiV Healthcare:[5]
- abacavir sulfate (ABC)
- lamivudine (3TC)
- zidovudine (AZT or ZDV)
It is indicated in the treatment of AIDS/HIV-1.[2] For this purpose, the combination is very useful in pregnant women to decrease the risk of mother-to-child transmission.[6]
The most common effects include headache and nausea (feeling sick).[3]
Abacavir/lamivudine/zidovudine was approved for use in the United States and the European Union in 2000.[7][3] In December 2013, Lupin Limited launched a generic version of abacavir/lamivudine/zidovudine.[8][9][10]
Side effects
[edit]The most common side effects of abacavir/lamivudine/zidovudine include nausea, vomiting, diarrhea, fatigue, paresthesia and headache. As with many medications targeting reverse transcriptase, body fat redistribution syndrome may occur, causing body fat to center on the upper back and neck, breast, and torso, and potentially decreasing around the legs, arms, and face.[11] IRIS may occur which is when the immune system initially improves, but then deteriorates as a previously ignored infection becomes active. Other serious side effects include:[12]
- Increased risk of heart attack
- Lactic acidosis
- Severe hepatomegaly
- Lipoatrophy
- Neutropenia
- Anemia
- Hypersensitivity reactions
- Includes liver failure, renal failure, anaphylaxis, hypotension, and death.
See also
[edit]References
[edit]- ^ "Abacavir / lamivudine / zidovudine (Trizivir) Use During Pregnancy". Drugs.com. 8 May 2018. Retrieved 7 April 2020.
- ^ a b c "Trizivir- abacavir sulfate, lamivudine, and zidovudine tablet, film coated". DailyMed. 10 May 2019. Retrieved 7 April 2020.
- ^ a b c d "Trizivir EPAR". European Medicines Agency (EMA). 29 January 2008. Retrieved 7 April 2020.
- ^ Opravil M, Hirschel B, Lazzarin A, Furrer H, Chave JP, Yerly S, et al. (May 2002). "A randomized trial of simplified maintenance therapy with abacavir, lamivudine, and zidovudine in human immunodeficiency virus infection". The Journal of Infectious Diseases. 185 (9): 1251–60. doi:10.1086/340312. PMID 12001042.
- ^ "GlaxoSmithKline-Pfizer launch HIV joint venture". InPharm.com. Archived from the original on 4 January 2012.
- ^ Horvath T, Madi BC, Iuppa IM, Kennedy GE, Rutherford G, Read JS (January 2009). "Interventions for preventing late postnatal mother-to-child transmission of HIV". The Cochrane Database of Systematic Reviews. 2009 (1): CD006734. doi:10.1002/14651858.CD006734.pub2. PMC 7389566. PMID 19160297.
- ^ "Drug Approval Package: Trizivir (abacavir sulfate, lamivudine, zidovudine) NDA #021205". U.S. Food and Drug Administration (FDA). 28 March 2004. Retrieved 7 April 2020.
- ^ Monthly Prescribing Reference (MPR)
- ^ "Abacavir Sulfate". Lupin Pharma.
- ^ "Abacavir sulfate, lamivudine and zidovudine: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Retrieved 6 July 2020.
- ^ ViiV Healthcare (March 2017). "Trizivir Medication Guide" (PDF). Archived (PDF) from the original on 22 December 2019.
- ^ "Side Effects of Trizivir (Abacavir Sulfate, Lamivudine, and Zidovudine), Warnings, Uses". RxList. Retrieved 22 December 2019.
External links
[edit]- "Abacavir sulfate mixture with lamivudine and zidovudine". Drug Information Portal. U.S. National Library of Medicine.