trizivir abacavir sulfate lamivudine and zidovudine tablet film coated

1 INDICATIONS AND USAGE TRIZIVIR is indicated in combination with other antiretrovirals or alone for the treatment of human immunodeficiency virus type 1 (HIV‑1) infection. Limitations of Use: • Limited data exist on the use of TRIZIVIR alone in patients with higher baseline viral load levels (greater than 100,000 copies per mL) [see Clinical Studies ( 14 )] . TRIZIVIR, a combination of abacavir, lamivudine, and zidovudine, each nucleoside analogue HIV-1 reverse transcriptase inhibitors, is indicated in combination with other antiretroviral agents for the treatment of HIV‑1 infection. ( 1 )

viiv healthcare company

FDA Reported Adverse Reactions
`[1] pain` `[2] drug ineffective` `[3] drug hypersensitivity` `[4] drug dependence` `[5] off label use` `[6] nausea` `[7] overdose` `[8] fatigue` `[9] toxicity to various agents` `[10] death`

4 weeks ago

OVAL BLUE GX LLI

16 HOW SUPPLIED/STORAGE AND HANDLING TRIZIVIR is available as tablets. Each tablet contains 300 mg of abacavir as abacavir sulfate, 150 mg of lamivudine, and 300 mg of zidovudine. The tablets are blue‑green capsule-shaped, film‑coated, and imprinted with GX LL1 on one side with no markings on the reverse side. They are packaged as follows: Bottles of 60 tablets (NDC 49702-217-18). Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F) (see USP Controlled Room Temperature).

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trizivir abacavir sulfate lamivudine and zidovudine tablet film coated

FDA Reported Adverse Reactions [1] pain [2] drug ineffective [3] drug hypersensitivity [4] drug dependence [5] off label use [6] nausea [7] overdose [8] fatigue [9] toxicity to various agents [10] death

OVAL BLUE GX LLI

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FDA Reported Adverse Reactions
`[1] pain` `[2] drug ineffective` `[3] drug hypersensitivity` `[4] drug dependence` `[5] off label use` `[6] nausea` `[7] overdose` `[8] fatigue` `[9] toxicity to various agents` `[10] death`