Azvudine is a Class 1.1 oral small-molecule antiviral innovative drug with completely independent intellectual property rights, developed by Henan Genuine Biotech Co., Ltd.; it is also the world’s first dual-target nucleoside anti-HIV-1 drug.
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Privacy Azvudine can clear viruses while activating the immune system to address both the symptoms and root causes. It achieves potent viral suppression at low doses, with low risk of drug resistance, predominantly mild adverse reactions, and favorable medication safety profile.
Azvudine, in combination with nucleoside reverse transcriptase inhibitors (NRTIs) and non-nucleoside reverse transcriptase inhibitors (NNRTIs), is indicated for the treatment of adult patients infected with HIV-1 who have a high viral load (HIV-1 RNA ≥ 100000copies/ml).
Initial treatment of HIV-1-infected patients should be conducted by physicians experienced in the treatment of HIV infection.
To ensure the correct dosage, the tablets should be swallowed whole and must not be crushed. The recommended dosage for adult patients is 3mg per dose, once daily, to be taken orally on an empty stomach before bedtime.
Contraindicated in patients hypersensitive to Azvudine or any other components of the formulation.
Study results indicate that single doses of 1mg to 5mg of Azvudine Tablets are safe and tolerable in HIV-infected patients. All adverse reactions reported are mild, mainly manifesting as fever, dizziness, nausea, diarrhea, etc. These reactions have all been documented with similar marketed anti-HIV drugs, and all symptoms resolve spontaneously or with symptomatic treatment.
During the 48-week administration period, all adverse reactions observed are common with marketed anti-HIV drugs, mainly including dizziness, elevated alanine aminotransferase (ALT), elevated γ-glutamyl transferase (GGT), and elevated aspartate aminotransferase (AST), with the severity mostly being Grade 1-2.
Studies on the use of this product in pregnant and lactating women have not been conducted.
Pediatric studies of this product have not been conducted.
Studies of this product in geriatric patients have not been conducted.
For more detailed drug information, please consult the official package leaflet.
If any issues arise, please contact us immediately.
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