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

Nevirapina Aurovitas

Active Ingredient:
Nevirapine
Origin:
EU

Nevirapina Aurovitas (Nevirapine)

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

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

Manufacturer / TM Owner

Aurovitas Spain,s.A.U.

1
Pack/s
This product is added to your enquiry list

Request a Quote

Please fill out the form below and our team will get back to you shortly with pricing and further information.

A minimum order value applies. Our team will confirm the exact amount or quantity after reviewing your requirements.

Indications & Clinical Uses

Nevirapine is an antiretroviral medication used to manage HIV‑1 infection by inhibiting viral replication.

  • Adult HIV‑1 infection: reduces viral load when combined with other antiretrovirals.
  • Pediatric HIV‑1 infection (≥2 years): part of combination therapy to control disease progression.
  • Prevention of mother‑to‑child transmission: used under specialist supervision to lower transmission risk during pregnancy and delivery.

How It Works

  • Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, inducing a conformational change that blocks the enzyme's activity. This inhibition prevents the conversion of viral RNA into DNA, thereby halting viral replication and reducing the amount of virus in the bloodstream.

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 stomach upset.
  • Fatigue: feeling of tiredness.
  • Headache: mild to moderate intensity.
  • Dizziness: transient light‑headedness.
  • Abdominal pain: discomfort in the stomach area.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate medical attention.
  • Hepatotoxicity: liver inflammation that may present with jaundice or elevated enzymes.
  • Severe hypersensitivity: systemic allergic response with fever and malaise.
  • Anaphylaxis: life‑threatening allergic reaction.
  • Hepatic failure: loss of liver function.
  • Severe rash: extensive skin involvement beyond mild eruptions.

Precautions & Warnings

Nevirapine requires careful monitoring due to potential risks.

  • Hepatic monitoring: assess liver function before initiation and periodically during therapy.
  • Skin reactions: discontinue if severe rash or signs of Stevens‑Johnson syndrome develop.
  • Pregnancy considerations: use only under specialist guidance due to possible fetal risk.
  • Drug resistance: avoid monotherapy and ensure adherence to combination regimens.
  • Concomitant medications: review all co‑administered drugs for interaction potential.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

Nevirapine interacts with several medicines that can alter its effectiveness or safety.

Major Interactions (Avoid)

  • Rifampicin: markedly reduces nevirapine plasma levels.
  • St. John's wort: induces metabolism, lowering drug exposure.
  • Protease inhibitors (e.g., ritonavir): can increase nevirapine concentrations leading to toxicity.
  • Carbamazepine: induces hepatic enzymes, decreasing nevirapine efficacy.
  • Efavirenz (high dose): may increase risk of hepatotoxicity.

Moderate Interactions (Monitor Closely)

  • Didanosine: combined use may heighten risk of pancreatitis.
  • Lamivudine: monitor for additive hepatic effects.
  • Warfarin: observe INR for potential changes.
  • Oral contraceptives: efficacy may be reduced; consider alternative contraception.

Frequently Asked Questions

Nevirapina Aurovitas contains nevirapine, an antiretroviral medication indicated for the treatment of HIV‑1 infection in adults and children as part of combination therapy. It helps lower viral load and improve immune function when used with other approved antiretroviral agents.

Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, causing a structural change that blocks the enzyme’s activity. This prevents the conversion of viral RNA into DNA, thereby inhibiting viral replication and reducing the amount of virus circulating in the bloodstream.

The specific dose of Nevirapina Aurovitas is determined by the prescribing clinician based on the patient’s age, weight, treatment history, and co‑administered medications. Healthcare professionals follow established guidelines and adjust the regimen according to clinical response and tolerability.

Nevirapine can be used during pregnancy only under specialist supervision because of potential risks to the fetus, particularly the possibility of liver toxicity and severe skin reactions. Breastfeeding decisions should be made in consultation with a healthcare provider, weighing the benefits of maternal therapy against any possible infant exposure.

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 (including any cold‑chain requirements), and necessary import documentation.

Nevirapine belongs to the NNRTI class, which directly inhibits reverse transcriptase at a non‑nucleoside site. Compared with nucleoside reverse transcriptase inhibitors (NRTIs), NNRTIs like nevirapine often have a different resistance profile and may cause distinct side‑effect patterns, such as skin rash and hepatic effects. Choice of regimen depends on patient factors, resistance testing, and tolerability.

Nevirapina Aurovitas should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original container, protect them from moisture and direct sunlight, and ensure the packaging remains tightly closed until use.

Nevirapina Aurovitas is administered orally, usually as a tablet taken with water. The prescribing clinician will provide instructions on timing relative to meals and other antiretroviral agents to optimise absorption and minimise side effects.

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 educated to report any rash, jaundice, dark urine, or unexplained fatigue promptly for medical evaluation.

Nevirapina Aurovitas 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:

Disclaimer

At GNH India, we aim to provide information that is expert-reviewed, accurate, and reliable. However, all content on this platform is intended for general informational purposes only and does not constitute professional medical advice, diagnosis, or treatment. While efforts are made to maintain accuracy and currency, the information may contain errors, omissions, or may not reflect the latest developments. Always consult a qualified healthcare professional regarding any medical concerns.

All product names, brand names, trademarks and registered trademarks displayed on this website are the property of their respective owners. This website and its operator are not affiliated with, endorsed by, or authorized by any such trade mark owners unless expressly stated. Any reference to product names or trademarks is made solely for descriptive and informational purposes. No commercial relationship, sponsorship, approval, or association with any trademark owner should be inferred. Information provided herein does not constitute promotion, advertising, or an offer for sale of any medicinal product and is intended solely for general informational purposes.

All trademarks and brand names displayed on this website are used strictly in accordance with the provisions of the Trade Marks Act, 1999, specifically Sections 30 and 30(1) governing fair use. Trademark ownership has been accurately attributed under the "Manufacturer/ TM Owner" section in compliance with statutory requirements.

Ordering Process

Simple, Secure, and Seamless

Learn how our streamlined ordering process guarantees fast, compliant, and reliable access to essential medicines worldwide.

Quote request form

01

Submit Quote Request Form

Tell us what medications you need by filling out our simple form and uploading a valid document.

Price estimate review

02

We Review & Send Estimate

Our licensed pharmacists will verify your details and provide you with a detailed cost estimate.

Secure payment

03

Confirm & Make Payment

Discuss any queries, approve the estimate, and complete your payment.

Worldwide delivery

04

Get Delivered

Your medicines, safely packed and delivered to your door or nearest airport — hassle-free.

Quality You Can Trust

Our internationally recognized certifications underscore our commitment to safety, quality, and excellence.