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

Nevirapina Farmoz

Active Ingredient:
Nevirapine
Origin:
EU

Nevirapina Farmoz (Nevirapine)

Nevirapine, the active ingredient in Nevirapina Farmoz, is a non‑nucleoside reverse transcriptase inhibitor presented as an oral tablet for oral use. It is used in the management of HIV‑1 infection in adults and adolescents, helping to suppress viral replication as part of combination antiretroviral therapy.

GNH India supplies Nevirapina Farmoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Deliveries are managed through established regulatory frameworks.

Manufacturer / TM Owner

Farmoz - Sociedade Técnico Medicinal, S.A.

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Indications & Clinical Uses

Nevirapine is an NNRTI used in the treatment of HIV‑1 infection, typically as part of combination antiretroviral regimens.

  • HIV‑1 infection (adult): Reduces viral load when combined with other antiretrovirals.
  • HIV‑1 infection (adolescent): Improves immune function as part of a pediatric regimen.
  • HIV‑1 infection (treatment‑experienced): Provides an alternative NNRTI option for patients with prior therapy.

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 plasma HIV levels when used with other antiretroviral agents.

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.
  • Fatigue: general feeling of tiredness.
  • Headache: transient cranial discomfort.
  • Insomnia: difficulty falling or staying asleep.
  • 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 rash: extensive or bullous skin lesions.
  • Hypersensitivity: systemic allergic response.
  • Neutropenia: marked reduction in white blood cells.
  • Anemia: significant drop in red blood cell count.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient-specific risk factors and monitor for adverse events.

  • Monitor liver function: baseline and periodic tests are recommended.
  • Assess for rash: discontinue if severe skin reactions develop.
  • Check for hepatitis B/C co‑infection: increased risk of hepatotoxicity.
  • Avoid use in patients with known hypersensitivity to nevirapine.
  • Pregnancy considerations: evaluate risk‑benefit under medical supervision.
  • Store at ambient temperature: keep below 25°C, protect from moisture and light.

Avoid Interactions

Nevirapine interacts with several drugs that affect its metabolism or increase toxicity risk.

Major Interactions (Avoid)

  • Ritonavir: potent CYP3A inhibition increases nevirapine levels.
  • Efavirenz: additive central nervous system toxicity.
  • St. John's wort: induces metabolism, reducing nevirapine efficacy.

Moderate Interactions (Monitor Closely)

  • Other protease inhibitors (except ritonavir): may alter nevirapine concentrations.
  • Anticonvulsants such as carbamazepine: may reduce nevirapine exposure.
  • Oral contraceptives: nevirapine may decrease hormonal efficacy, requiring additional contraception.

Frequently Asked Questions

Nevirapina Farmoz contains nevirapine, an NNRTI indicated for the treatment of HIV‑1 infection. It is prescribed as part of combination antiretroviral therapy to suppress viral replication in adults and adolescents.

Nevirapine binds to a non‑nucleoside site on HIV‑1 reverse transcriptase, causing a conformational change that blocks the enzyme’s RNA‑dependent DNA polymerase activity. This inhibition prevents the virus from converting its RNA into DNA, thereby halting replication.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s clinical status, weight, and treatment history. Healthcare providers follow established guidelines and adjust therapy as needed.

Safety in pregnancy and lactation must be evaluated by a qualified healthcare professional. Nevirapine may be used when the benefits outweigh potential risks, but clinicians should monitor liver function and counsel patients on possible adverse effects.

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 shares the NNRTI class with drugs such as efavirenz and rilpivirine. Compared with efavirenz, nevirapine has a lower incidence of central nervous system side effects but a higher risk of rash and hepatic toxicity, making patient‑specific factors important when selecting therapy.

Nevirapina Farmoz should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct light, and discard any product that shows signs of damage or degradation.

The medication is taken orally, usually with food to improve tolerability. Tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed by a healthcare professional.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, hepatic failure, hypersensitivity reactions, and hematologic abnormalities like neutropenia or anemia. Prompt medical attention is required if any of these symptoms occur.

Nevirapina Farmoz is contraindicated in patients with known hypersensitivity to nevirapine or any component of the formulation, and in individuals with severe liver disease or active hepatitis B/C infection due to increased risk of hepatotoxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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