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Dolutegravir Emtricitabine and Tenofovir Alafenamide Tablets

Dolutegravir Emtricitabine and Tenofovir Alafenamide Tablets

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उत्पाद वर्णन

The combination of Dolutegravir (DTG), Emtricitabine (FTC), and Tenofovir Alafenamide (TAF) is a commonly used antiretroviral medication for the treatment of HIV-1 infection. This combination is often provided in a fixed-dose tablet to simplify the treatment regimen for individuals living with HIV.

Here are some key points about Dolutegravir, Emtricitabine, and Tenofovir Alafenamide tablets:

  1. Dolutegravir (DTG):

    • DTG is an integrase strand transfer inhibitor (INSTI).
    • It inhibits the integrase enzyme, preventing the integration of viral DNA into the host cell genome, which is necessary for the replication of the HIV virus.
  2. Emtricitabine (FTC):

    • FTC is a nucleoside reverse transcriptase inhibitor (NRTI).
    • It inhibits the reverse transcriptase enzyme, disrupting the replication of the HIV virus.
  3. Tenofovir Alafenamide (TAF):

    • TAF is a prodrug of tenofovir, and it is a nucleotide reverse transcriptase inhibitor (NRTI).
    • TAF is an alternative to Tenofovir Disoproxil Fumarate (TDF), and it has a more favorable safety profile regarding potential effects on bone and kidney health.

Key points about the combination (Dolutegravir, Emtricitabine, and Tenofovir Alafenamide tablets):

  • Indications: This combination is used for the treatment of HIV-1 infection in adults and pediatric patients.

  • Dosage: The typical dosage involves taking one tablet orally once daily. The specific dosage may vary depending on the individual's health condition and the overall HIV treatment plan prescribed by a healthcare professional.

  • Adherence: Consistent adherence to the prescribed regimen is crucial for the effectiveness of HIV treatment. Missing doses or not taking the medication as directed can lead to reduced efficacy and the development of drug resistance.

  • Side Effects: Potential side effects may include nausea, headache, and fatigue. It's important to report any severe or persistent side effects to a healthcare provider.

  • Pregnancy: The use of this combination during pregnancy should be discussed with a healthcare provider, taking into consideration the potential risks and benefits.

Individuals prescribed with this combination should follow the guidance of their healthcare provider, undergo regular monitoring, and communicate any concerns or side effects experienced during the treatment. As always, individual circumstances may vary, and healthcare providers can provide personalized information based on the patient's medical history and needs

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