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Generic Triumeq ( Abacavir/dolutegravir/lamivudine )
Triumeq is a fixed‑dose combination tablet containing abacavir (600 mg), dolutegravir (50 mg), and lamivudine (300 mg). It is indicated for the treatment of human immunodeficiency virus type 1 (HIV‑1) infection in adults and adolescents weighing at least 25 kg. Abacavir and lamivudine are nucleoside reverse transcriptase inhibitors (NRTIs) that are phosphorylated intracellularly and inhibit HIV‑1 reverse transcriptase by competing with natural nucleotides and causing chain termination. Dolutegravir is an integrase strand transfer inhibitor (INSTI) that blocks the HIV integrase enzyme, preventing the insertion of proviral DNA into the host genome. The three‑drug combination provides a complete once‑daily antiretroviral regimen that can suppress viral replication and maintain long‑term virologic control. Triumeq is not a cure for HIV.
Usual adult dose: One tablet (abacavir 600 mg / dolutegravir 50 mg / lamivudine 300 mg) taken orally once daily, with or without food. The tablet should be swallowed whole; it may be split in half if necessary to facilitate swallowing, but both halves must be taken immediately. Triumeq must not be used in patients who require dosage adjustments of individual components, and it is not recommended for patients with creatinine clearance less than 50 mL/min. Before starting therapy, all patients must be screened for the HLA‑B*5701 allele; Triumeq is contraindicated in patients who test positive because of the high risk of a potentially fatal hypersensitivity reaction to abacavir. If a dose is missed, the patient should take it as soon as remembered, but two doses must never be taken on the same day. Co‑administration with dofetilide is contraindicated, and dolutegravir requires careful management when co‑administered with certain anticonvulsants, rifampin, or antacids containing polyvalent cations. Triumeq must always be used as a complete regimen; no additional antiretroviral is required unless specified by a specialist.
Dosage form: Film‑coated tablets: each tablet contains abacavir 600 mg (as abacavir sulfate), dolutegravir 50 mg (as dolutegravir sodium), and lamivudine 300 mg. The tablet is purple, biconvex, oval‑shaped, and debossed with “572 Tri” on one side. Available in bottles of 30 tablets.
Onset of action: Rapid antiviral activity is observed; significant decreases in plasma HIV‑1 RNA are typically seen within the first 2 to 4 weeks of initiating treatment, with most adherent patients achieving viral suppression (less than 50 copies/mL) by 16 to 24 weeks.
Duration of action: Once‑daily dosing sustains plasma and intracellular concentrations within the therapeutic range over the 24‑hour interval. The elimination half‑lives are approximately 1.5 hours for abacavir, 14 hours for dolutegravir, and 5 to 7 hours for lamivudine, but the pharmacodynamic effect is prolonged and maintained with consistent daily adherence.
Alcohol recommendation: Alcohol should be limited or avoided during treatment with Triumeq. Alcohol may increase the plasma exposure of abacavir by approximately 40%, potentially heightening the risk of adverse events. Additionally, excessive alcohol intake can impair hepatic function and adherence to therapy. Patients with pre‑existing liver disease should exercise particular caution.
Most common side effects: Insomnia, headache, nausea, diarrhea, fatigue, and dizziness. These are generally mild to moderate and often resolve within the first few weeks. The most important serious risk is the abacavir hypersensitivity reaction, which can be life‑threatening and is characterized by fever, rash, gastrointestinal symptoms (nausea, vomiting, diarrhea, abdominal pain), respiratory symptoms (dyspnea, sore throat, cough), and constitutional symptoms (malaise, fatigue, myalgia). Any patient in whom hypersensitivity is suspected must discontinue Triumeq immediately and never be rechallenged. Dolutegravir has been associated with small, non‑progressive increases in serum creatinine due to inhibition of renal tubular secretion of creatinine, which does not reflect a true decline in glomerular filtration rate. Elevations in hepatic transaminases and, rarely, hypersensitivity reactions including rash and organ dysfunction have been reported. As with all effective antiretroviral therapy, immune reconstitution inflammatory syndrome (IRIS) may occur, and body fat redistribution has been observed. Lamivudine has a well‑established safety profile; however, severe acute exacerbations of hepatitis B have been reported in patients co‑infected with HIV and HBV who discontinue lamivudine‑containing regimens; liver function must be closely monitored if Triumeq is stopped. Triumeq is not a cure for HIV and does not prevent transmission of the virus. In Canada, Triumeq is available only by prescription and must be prescribed by a healthcare professional experienced in HIV management.
Would you like to try Triumeq (Abacavir/dolutegravir/lamivudine) without a prescription?
+ Package delivery insurance
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+ Package delivery insurance
+ Next orders 10% discount
+ Package delivery insurance
+ Next orders 10% discount
