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Tenvir-EM

HIV-AIDS-Cipla-Tenofovir-300mg-Emtricitabine-200mg-Tenvir-EM

Availability: In stock

Special Price $ 45

BRAND : Tenvir-EM
STRENGTH : 300mg & 200mg
INGREDIENT : HIV-AIDS-Cipla-Tenofovir-300mg-Emtricitabine-200mg-Tenvir-EM
COMPANY NAME : Cipla
COUNT : 30 Tablets



Description of Tenvir-EM

Tenvir-EM



BRAND : Tenvir-EM
STRENGTH : 300mg & 200mg
INGREDIENT : HIV-AIDS-Cipla-Tenofovir-300mg-Emtricitabine-200mg-Tenvir-EM
COMPANY NAME : Cipla
COUNT : 30 Tablets

Indication:

Tenvir-EM tablet is manufactured by cipla which is an antiviral drugs that work by preventing HIV (human immunodeficiency virus) cells from multiplying in the body.

Tavin-EM (Tenofovir 300mg/Emtricitabine 200mg) is a combination medicine used to treat HIV, the virus that can cause acquired immunodeficiency syndrome (AIDS). This medicine is not a cure for HIV or AIDS, but it can be used to treat HIV in adults and children who are at least 12 years old and weigh at least 17 kilograms (37 pounds).

Tenofovir:

Tenofovir inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5’-triphosphate and, after incorporation into DNA, by DNA chain termination. Specifically, the drugs are analogues of the naturally occurring deoxynucleotides needed to synthesize the viral DNA and they compete with the natural deoxynucleotides for incorporation into the growing viral DNA chain. However, unlike the natural deoxynucleotides substrates, NRTIs and NTRTIs (nucleoside/tide reverse transcriptase inhibitors) lack a 3'-hydroxyl group on the deoxyribose moiety. As a result, following incorporation of an NRTI or an NtRTI, the next incoming deoxynucleotide cannot form the next 5'-3' phosphodiester bond needed to extend the DNA chain. Thus, when an NRTI or NtRTI is incorporated, viral DNA synthesis is halted, a process known as chain termination. All NRTIs and NtRTIs are classified as competitive substrate inhibitors.

Emtricitabine:

Emtricitabine works by inhibiting reverse transcriptase, the enzyme that copies HIV RNA into new viral DNA. Emtricitabine is a synthetic nucleoside analogue of cytidine. It is phosphorylated by cellular enzymes to form emtricitabine 5'-triphosphate, which is responsible for the inhibition of HIV-1 reverse transcriptase. It competes with the natural substrate deoxycytidine 5'-triphosphate and incorporates into nascent viral DNA, resulting in early chain termination. Therefore emtricitabine inhibits the activity of HIV-1 reverse transcriptase (RT) both by competing with the natural substrate deoxycytidine 5'-triphosphate and by its incorporation into viral DNA. By inhibiting HIV-1 reverse transcriptase, emtricitabine can help to lower the amount of HIV, or "viral load", in a patient's body and can indirectly.

Side effects:

Nausea, vomiting, diarrhea, headache, dizziness, trouble sleeping, back pain, or change in the color of skin on your palms or soles of your feet may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

Pharmacology of Tenvir-EM

Indication of Tenvir-EM

Dose & Dosage's of Tenvir-EM

Side Effects of Tenvir-EM

Contraindication of Tenvir-EM

Drug Interaction of Tenvir-EM

Precaution of Tenvir-EM

Usage & Safety profile of Tenvir-EM Pregnancy & Lactation

Storage of Tenvir-EM