Product image of Nevirapina Generis (Nevirapine) supplied by GNH India

Nevirapina Generis

Active Ingredient:
Nevirapine
Origin:
EU

Nevirapina Generis (Nevirapine)

Nevirapine, the active ingredient in Nevirapina Generis, is a Non‑nucleoside reverse transcriptase inhibitor (NNRTI) presented as an oral tablet for oral use. It is employed in the treatment of HIV‑1 infection, typically as part of combination antiretroviral therapy, and is indicated for adults and children living with the virus.

GNH India supplies Nevirapina Generis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Generis Farmacêutica, S.A.

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Indications & Clinical Uses

Nevirapine is an antiretroviral drug that targets HIV‑1 reverse transcriptase, a key enzyme in the viral replication cycle.

  • HIV‑1 infection: suppresses viral replication when used in combination antiretroviral regimens.
  • AIDS: helps improve immune function and reduce opportunistic infections as part of therapy.
  • Prevention of mother‑to‑child transmission: reduces the risk of vertical HIV transmission when administered to pregnant women in combination therapy.

How It Works

  • Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, inducing conformational changes that inhibit its activity. This blockade prevents the conversion of viral RNA into DNA, thereby halting the synthesis of proviral DNA and interrupting the HIV replication cycle.

Side Effects

Nevirapine may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Rash: mild to moderate skin eruptions.
  • Nausea: occasional gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Fatigue: general tiredness.
  • Dizziness: occasional light‑headedness.
  • Abdominal pain: mild stomach discomfort.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate discontinuation.
  • Hepatic failure: signs of liver toxicity such as jaundice.
  • Severe hypersensitivity: systemic allergic response.
  • Anaphylaxis: life‑threatening allergic reaction.
  • Hepatotoxicity: elevated liver enzymes and possible liver injury.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Monitor liver function: obtain baseline and periodic liver enzyme tests.
  • Assess for rash: discontinue promptly if severe cutaneous reactions develop.
  • Avoid in known hypersensitivity: do not prescribe to patients with prior nevirapine allergy.
  • Use caution in pregnancy: limited safety data; weigh benefits against potential risks.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Nevirapine interacts with several drugs that can alter its plasma levels or increase toxicity.

Major Interactions (Avoid)

  • Rifampicin: induces metabolism, markedly reducing nevirapine concentrations.
  • St. John’s wort: herbal inducer that lowers nevirapine exposure.
  • Protease inhibitors (e.g., ritonavir): increase nevirapine levels, raising toxicity risk.

Moderate Interactions (Monitor Closely)

  • Efavirenz: may enhance central nervous system side effects.
  • Zidovudine: combined use can affect hematologic parameters.
  • Didanosine: concurrent therapy may increase risk of pancreatitis.

Frequently Asked Questions

Nevirapina Generis contains nevirapine, an NNRTI that is prescribed to treat HIV‑1 infection. It is used as part of combination antiretroviral therapy to suppress viral replication and improve immune function in adults and children living with HIV.

Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, causing a conformational change that blocks the enzyme’s activity. This inhibition prevents the conversion of viral RNA into DNA, thereby halting the production of new viral particles.

The specific dose and dosing schedule of Nevirapina Generis are determined by the prescribing clinician based on the patient’s age, weight, treatment history, and co‑administered antiretrovirals. Only a qualified healthcare professional should set the regimen.

Safety data for nevirapine in pregnancy are limited, and the drug is classified as having an unknown pregnancy category. Clinicians must weigh potential benefits against risks, and breastfeeding decisions should follow local guidelines and professional advice.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Nevirapine belongs to the NNRTI class, which directly inhibits reverse transcriptase, unlike nucleoside reverse transcriptase inhibitors (NRTIs) that act as chain terminators. Compared with efavirenz, another NNRTI, nevirapine has a lower incidence of central nervous system side effects but a higher risk of skin and hepatic reactions.

Nevirapina Generis should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiry date.

Nevirapina Generis is taken orally, usually as a tablet, with or without food as directed by the prescriber. Consistent daily dosing at the same time each day helps maintain stable drug levels.

The most serious risks include severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and potentially life‑threatening liver toxicity. Patients should be monitored closely for rash, jaundice, or any signs of hepatic dysfunction, and the drug should be stopped immediately if these occur.

Nevirapina Generis is contraindicated in individuals with a known hypersensitivity to nevirapine or any component of the formulation. It should also be avoided in patients with pre‑existing severe hepatic impairment or a history of severe cutaneous adverse reactions to NNRTIs.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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