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

Nevirapina Accord

Active Ingredient:
Nevirapine
Origin:
EU

Nevirapina Accord (Nevirapine)

Nevirapine, the active ingredient in Nevirapina Accord, is a non‑nucleoside reverse transcriptase inhibitor presented as an oral tablet for oral use. It is indicated for the treatment of HIV‑1 infection in adults and adolescents and is used as part of combination antiretroviral therapy.

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

Manufacturer / TM Owner

Accord Healthcare Polska Sp. Z O.O.

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Indications & Clinical Uses

Nevirapine is a non‑nucleoside reverse transcriptase inhibitor used in the management of HIV‑1 infection.

  • HIV‑1 infection (treatment‑naïve adults): reduces viral load and delays disease progression.
  • HIV‑1 infection (treatment‑experienced adults): provides an alternative regimen when resistance develops.
  • Prevention of mother‑to‑child transmission of HIV‑1: lowers the risk of vertical transmission when combined with other antiretrovirals.

How It Works

  • Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, inducing conformational changes that inhibit the enzyme’s RNA‑dependent DNA polymerase activity. This blockade 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. Patients should be monitored for any new symptoms during therapy.

Common Side Effects

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

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate discontinuation.
  • Toxic epidermal necrolysis: life‑threatening skin detachment.
  • Severe hepatic injury: marked elevation of liver enzymes or hepatitis.
  • Hypersensitivity reactions: fever, eosinophilia, or organ involvement.
  • Grade 3/4 neutropenia: significant reduction in white blood cells.
  • Lactic acidosis: rare metabolic disturbance.

Precautions & Warnings

Nevirapine requires careful monitoring to minimize risks and ensure safe use.

  • Liver function monitoring: assess baseline and periodic liver enzymes.
  • Skin reactions: discontinue immediately if severe rash or mucosal involvement occurs.
  • Hepatic risk: avoid in patients with active hepatitis or severe liver disease.
  • Drug interactions: review concomitant medications, especially CYP inducers or inhibitors.
  • Pregnancy and breastfeeding: evaluate risk‑benefit ratio before use.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Ritonavir: potent CYP3A4 inhibition can raise nevirapine concentrations.
  • St. John’s wort: strong CYP3A4 induction may reduce nevirapine effectiveness.

Moderate Interactions (Monitor Closely)

  • Efavirenz: additive central nervous system effects may increase neuropsychiatric symptoms.
  • Zidovudine: combined use may heighten risk of hepatotoxicity.
  • Oral contraceptives: nevirapine may decrease hormonal contraceptive efficacy.

Frequently Asked Questions

Nevirapina Accord contains nevirapine, an NNRTI antiretroviral medication used as part of combination therapy to treat HIV‑1 infection in adults and adolescents, and to help prevent mother‑to‑child transmission when used with other agents.

Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, causing a conformational change that blocks the enzyme’s ability to copy viral RNA into DNA, thereby inhibiting viral replication.

The specific dosing regimen for Nevirapina Accord is determined by the prescribing clinician based on the patient’s clinical status, treatment history, and current guidelines. Patients should follow the prescriber’s instructions exactly.

Nevirapine may be used during pregnancy or breastfeeding only after a careful risk‑benefit assessment by a qualified healthcare professional. Potential benefits for preventing HIV transmission must be weighed against possible maternal and infant risks.

To 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 at a non‑nucleoside site. Compared with nucleoside reverse transcriptase inhibitors (NRTIs), NNRTIs like nevirapine have a distinct resistance profile and are often combined with NRTIs to achieve synergistic viral suppression.

Nevirapina Accord should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, heat and direct sunlight to maintain stability.

Nevirapina Accord is taken orally, usually with food to improve tolerability. The tablet should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed by a healthcare provider.

The most serious risks include severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and potentially life‑threatening liver injury. Prompt medical attention is required if symptoms of rash, fever, jaundice or unexplained fatigue develop.

Nevirapina Accord is contraindicated in patients with known hypersensitivity to nevirapine or any component of the formulation, and in individuals with severe hepatic impairment or active hepatitis. Clinicians should also avoid use in patients with a history of severe skin reactions to NNRTIs.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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