Névirapine Teva
Névirapine Teva Uses, Dosage, Side Effects, Food Interaction and all others data.
Névirapine Teva is a non-nucleoside reverse transcriptase inhibitor that acts against HIV-1. It binds directly to reverse transcriptase and thereby blocks the RNA-dependent and DNA-dependent DNA polymerase activities by disrupting the enzyme's catalytic site.
Névirapine Teva is a non-nucleoside reverse transcriptase inhibitor (nNRTI) with activity against Human Immunodeficiency Virus Type 1 (HIV-1). HIV-2 RT and eukaryotic DNA polymerases (such as human DNA polymerases alpha, beta, or sigma) are not inhibited by nevirapine. Névirapine Teva is, in general, only prescribed after the immune system has declined and infections have become evident. It is always taken with at least one other HIV medication such as Retrovir or Videx. The virus can develop resistance to nevirapine if the drug is taken alone, although even if used properly, nevirapine is effective for only a limited time.
Trade Name | Névirapine Teva |
Availability | Prescription only |
Generic | Nevirapine |
Nevirapine Other Names | Nevirapina, Nevirapine |
Related Drugs | Biktarvy, Truvada, tenofovir, ritonavir, zidovudine, Complera, Atripla, Stribild, Retrovir |
Type | |
Formula | C15H14N4O |
Weight | Average: 266.2979 Monoisotopic: 266.11676109 |
Protein binding | 60% bound to plasma protein. |
Groups | Approved |
Therapeutic Class | Drugs for HIV / Anti-retroviral drugs |
Manufacturer | |
Available Country | France, Netherlands |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Névirapine Teva is used for combination antiretroviral treatment of HIV-1 infection in adults and in pediatric patients 15 days and older.
Additional important information regarding the use of Névirapine Teva for the treatment of HIV-1 infection:
- Based on serious and life-threatening hepatotoxicity observed in controlled and uncontrolled trials, Névirapine Teva should not be initiated in adult females with CD4+ cell counts greater than 250 cells/mm³ or in adult males with CD4+ cell counts greater than 400 cells/mm³ unless the benefit outweighs the risk.
- The 14-day lead-in period with Névirapine Teva 200 mg daily dosing must be strictly followed; it has been demonstrated to reduce the frequency of rash.
- If rash persists beyond the 14-day lead-in period, do not dose escalate to 200 mg twice daily. The 200 mg once-daily dosing regimen should not be continued beyond 28 days, at which point an alternative regimen should be sought.
Névirapine Teva is also used to associated treatment for these conditions: Human Immunodeficiency Virus (HIV) Infections
How Névirapine Teva works
Névirapine Teva binds directly to reverse transcriptase (RT) and blocks the RNA-dependent and DNA-dependent DNA polymerase activities by causing a disruption of the enzyme's catalytic site. The activity of nevirapine does not compete with template or nucleoside triphosphates.
Dosage
Névirapine Teva dosage
Adult Patients: The recommended dose for Névirapine Teva is one 200 mg tablet daily for the first 14 days, followed by one 200 mg tablet twice daily, in combination with other antiretroviral agents. The lead-in period has been observed to decrease the incidence of rash. For concomitantly administeredantiretroviral therapy, the manufacturer's recommended dosage and monitoring should be followed.
Pediatric Patients: The recommended oral dose for pediatric patients 15 days and older is 150 mg/m² once daily for 14 days followed by 150 mg/m² twice daily thereafter. The total daily dose should not exceed 400 mg for any patient.
Side Effects
Skin rash, nausea, vomiting, headache, abnormal LFT, fatigue, diarrhoea, abdominal pain.
Toxicity
Symptoms of overdose include edema, erythema nodosum, fatigue, fever, headache, insomnia, nausea, pulmonaryinfiltrates, rash, vertigo, vomiting, and weight decrease. The most common adverse reaction is rash.
Precaution
Caution should be taken during pregnancy. Interrupt treatment if severe hepatotoxicity or life-threatening skin reactions develop. Renal or hepatic insufficiency. Monitor liver function periodically.
Interaction
Mutually increased levels effects when used with drugs extensively metabolised by CYP3A. Reduced levels/effects of methadone.
Food Interaction
- Avoid alcohol.
- Take with or without food. The absorption is unaffected by food.
Névirapine Teva Drug Interaction
Moderate: testosterone, phenytoin, alprazolamUnknown: aspirin, aspirin, aspirin, emtricitabine / tenofovir alafenamide, metoprolol, acetaminophen, emtricitabine / tenofovir, valproic acid, multivitamin, thiamine, cyanocobalamin, riboflavin, pyridoxine, ascorbic acid, cholecalciferol, phytonadione, zinc sulfate
Névirapine Teva Disease Interaction
Major: hepatotoxicity, rashModerate: hemodialysis, renal dysfunction
Volume of Distribution
- 1.21 ± 0.09 L/kg [apparent volume of distribution, healthy adults, IV] Névirapine Teva is capable of crossing the placenta and is found in breast milk.
Elimination Route
Névirapine Teva is readily absorbed (greater than 90%) after oral administration in healthy subjects and adults with HIV-1 infection. The absolute bioavailability in healthy adults following a single dose administration is 93 ± 9% (mean ± SD) for a 50 mg tablet and 91 ± 8% for an oral solution. Peak plasma nevirapine concentrations of 2 ± 0.4 mcg/mL (7.5 micromolar) were attained by 4 hours following a single 200 mg dose. Névirapine Teva tablets and suspension have been shown to be comparably bioavailable and interchangeable at doses up to 200 mg. When the oral tablet is given with a high-fat meal, the extent of absorption is compared to that of the fasted-state.
Half Life
45 hours
Elimination Route
Thus cytochrome P450 metabolism, glucuronide conjugation, and urinary excretion of glucuronidated metabolites represent the primary route of nevirapine biotransformation and elimination in humans. Only a small fraction (<5%) of the radioactivity in urine (representing <3% of the total dose) was made up of parent compound; therefore, renal excretion plays a minor role in elimination of the parent compound.
Pregnancy & Breastfeeding use
Nursing Mothers: The Centers for Disease Control and Prevention recommend that HIV-1 infected mothers not breastfeed their infants to avoid risking postnatal transmission of HIV-1. Névirapine Teva is excreted in breast milk. Because of both the potential for HIV-1 transmission and the potential for serious adverse reactions in nursing infants, mothers should be instructed not to breastfeed if they are receiving Névirapine Teva.
Contraindication
Hypersensitivity. Lactation. Severe hepatic impairment.
Special Warning
Pediatric Use: The safety, pharmacokinetic profile, and virologic and immunologic responses of Névirapine Teva have been evaluated in HIV-1 infected pediatric subjects age 3 months to 18 years. The safety and pharmacokinetic profile of Névirapine Teva has been evaluated in HIV-1 infected pediatric subjects age 15 days to less than 3 months.
The most frequently reported adverse events related to Névirapine Teva in pediatric subjects were similar to those observed in adults, with the exception of granulocytopenia, which was more commonly observed in children receiving both zidovudine and Névirapine Teva.
Geriatric Use: Clinical trials of Névirapine Teva did not include sufficient numbers of subjects aged 65 and older to determine whether elderly subjects respond differently from younger subjects. In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy.
Renal Impairment: In subjects with renal impairment (mild, moderate or severe), there were no significant changes in the pharmacokinetics of nevirapine. Névirapine Teva is extensively metabolized by the liver and nevirapine metabolites are extensively eliminated by the kidney. Névirapine Teva metabolites may accumulate in patients receiving dialysis; however, the clinical significance of this accumulation is not known. No adjustment in nevirapine dosing is required in patients with CrCL greater than or equal to 20 mL per min. The pharmacokinetics of nevirapine have not been evaluated in patients with CrCl less than 20 mL per min. In patients undergoing chronic hemodialysis, an additional 200 mg dose following each dialysis treatment is indicated.
Hepatic Impairment: Because increased nevirapine levels and nevirapine accumulation may be observed in patients with serious liver disease, do not administer Névirapine Teva to patients with moderate or severe (Child-Pugh Class B or C, respectively) hepatic impairment.
Acute Overdose
There is no known antidote for Névirapine Teva overdosage. Cases of Névirapine Teva overdose at doses ranging from 800 to 1800 mg per day for up to 15 days have been reported. Patients have experienced events including edema, erythema nodosum, fatigue, fever, headache, insomnia, nausea, pulmonary infiltrates, rash, vertigo, vomiting, and weight decrease. All events subsided following discontinuation of Névirapine Teva.
Storage Condition
Store at 15-30° C
Innovators Monograph
You find simplified version here Névirapine Teva
Névirapine Teva contains Nevirapine see full prescribing information from innovator Névirapine Teva Monograph, Névirapine Teva MSDS, Névirapine Teva FDA label