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15 Days Easy
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(>8 Months)
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Spegra Tablet 90s (Dolutegravir + Emtricitabine + Tenofovir Alafenamide) is a complete, fixed-dose combination (FDC) antiretroviral therapy (ART) used for the treatment of Human Immunodeficiency Virus Type 1 (HIV-1) infection. This single-tablet regimen combines three potent antiviral agents from two different classes: Dolutegravir, an Integrase Strand Transfer Inhibitor (INSTI), and two Nucleoside Reverse Transcriptase Inhibitors (NRTIs), Emtricitabine and Tenofovir Alafenamide. This combination is designed to suppress the viral load to undetectable levels, preserve immune function (CD4 count), and prevent the progression of HIV to AIDS. It is highly regarded for its high genetic barrier to resistance, potency, and improved safety profile, specifically regarding bone and kidney health, compared to older Tenofovir-based regimens.
Spegra Tablet 90s provides a simplified "one-pill, once-a-day" solution for managing a chronic viral infection. It targets multiple stages of the HIV life cycle, making it difficult for the virus to replicate and mutate.
Spegra Tablet 90s (Dolutegravir + Emtricitabine + Tenofovir Alafenamide) is indicated for:
As a complete regimen for adults and pediatric patients (weighing at least 35kg) who are new to treatment (treatment-naive) or to replace a current stable regimen in those who are virologically suppressed.
Maintaining an undetectable viral load to prevent transmission and immune system decline.
Dolutegravir ensures the virus remains suppressed even if the patient occasionally struggles with perfect adherence.
Tenofovir Alafenamide (TAF) offers superior bone and renal safety compared to older HIV medications.
A single-tablet, once-daily regimen significantly improves treatment adherence and quality of life.
Clinical trials show that this combination brings viral loads down to undetectable levels more quickly than many other regimens.
The medication blocks HIV replication at two distinct steps:
Dolutegravir is now generally considered safe for use throughout pregnancy, but a risk-benefit assessment by a specialist is mandatory.
In many regions, breastfeeding is discouraged for mothers with HIV to prevent transmission to the infant; follow local clinical guidelines.
May cause dizziness or insomnia in some patients; ensure you know how the drug affects you before operating vehicles.
Monitor liver enzymes regularly; patients with Hepatitis B or C are at higher risk for hepatotoxicity.
While TAF is safer for the kidneys, renal function (creatinine/eGFR) should be monitored periodically during therapy.
Avoid excessive alcohol as it can increase the risk of liver strain and may worsen side effects like dizziness.
The recommended dose is one tablet (50mg/200mg/25mg) orally once daily.
In case of an overdose, contact a poison control centre or emergency room immediately. Symptoms may include severe dizziness or exaggerated side effects. Treatment is generally supportive.
Therapeutic Class
Antiretroviral (HIV-1)
Action Class
Integrase and Reverse Transcriptase Inhibitors
Chemical Class
INSTI + NRTI + NRTI
Habit Forming
No
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