- HIV 1 infection in combination with other antivirals:
- Adults & >16 years: PO 200mg OD *2/52, then if no rash increase to 200mg BD
- If rash occurs wait until it is resolved before increasing
- Adults & >16 years: PO 200mg OD *2/52, then if no rash increase to 200mg BD
-
- ≥15 days- 6 years: PO 150mg/m² OD *2/52, then if no rash, then increase to 150mg/m² BD
- Max 200mg/dose
- ≥15 days- 6 years: PO 150mg/m² OD *2/52, then if no rash, then increase to 150mg/m² BD
- Prevention of maternal-fetal HIV transmission in women with no prior antiretroviral treatment:
- PO 200mg as a single dose at onset of labor
- Used with IV zidovudine
- PO 200mg as a single dose at onset of labor
- Prevention of maternal-fetal HIV transmission in neonates (3 drug regimen):
- 34-37 wk gestation: PO 8mg/kg/day divided BD*1/52, then 12mg/kg/day BD *1-5 weeks
- >37 week gestation: PO 12mg/kg/day divided BD *2-6 weeks
- Initiated within 12 hours after birth
- Given with lamivudine and zidovudine
- Prevention of maternal-fetal HIV transmission in neonates (2 drug regimen):
- Birth weight 1.5-2 kg: PO 8mg/dose
- Birth weight >2 kg: PO 12mg/dose
- Administer 3 doses in the first week of life, 1st dose 48 hours after birth, give 2nd dose 48 hours after 1st dose and 3rd dose 96 hours after 2nd dose
- Recommended in combination with 6 weeks of zidovudine
- Tablet:
- 200mg
- Suspension:
- 50mg/5mL
- Shake suspension gently and administer entire measured dose
- To be taken with/without food
Non-nucleoside Reverse Transcriptase Inhibitors (NNRTIs)
It inhibits reverse transcriptase and incorporates into viral DNA resulting in DNA chain termination
- Rash
- Nausea
- Elevated ALT/AST
- Fatigue
- Headache
- Anemia
- Diarrhea
- Abdominal pain
- Hepatotoxicity
- Arthralgia
- Myalgia
- Lipodystrophy
- Pregnancy (treatment-naive patients)
- Post-exposure prophylaxis use
- Hepatic impairment, Child-Pugh Class B-C
- Baseline CD4 >250 (female patients)
- Baseline CD4 >400 (male patients)
- Breastfeeding
WARNING
- Severe, life-threatening and sometimes fatal hepatotoxicity
- Severe, life-threatening and sometimes fatal skin reactions including Steven-Johnson syndrome, toxic epidermal necrolysis, hypersensitivity reactions with rash, constitutional findings and organ dysfunction
- Extra vigilance warranted during first 6 week of therapy (period of greatest risk)
- Artemether/lumefantrine
- Atazanavir
- Carbamazepine
- Cariprazine
- Cobimetinib
- Dienogest/estradiol valerate
- Doravirine
- Efavirenz
- Elbasvir/grazoprevir
- Elvitegravir/cobicistat/emtricitabine/tenofovir df
- Etravirine
- Lumacaftor/ivacaftor
- Lumefantrine
- Lurasidone
- Naloxegol
- Ombitasvir/paritaprevir/ritonavir & dasabuvir
- Panobinostat
- Praziquantel
- Regorafenib
- Rilpivirine
- Roflumilast
- Vandetanib
Drug Status
Availability | Prescription only |
Pregnancy | Contraindicated in treatment-naive patients; Category B |
Breastfeeding | Contraindicated |
Schedule | Not controlled |
BRAND NAME | STRENGTH | FORMULATION | PACK SIZE | MANUFACTURER | DISTRIBUTOR |
---|---|---|---|---|---|
Nevimune | 200mg | Tablet | 60’s | Cipla Limited | Cipla Limited |
Nevimune | 50mg/5mL | Suspension | 100mL | Cipla Limited | Cipla Limited |
Nevirapine | 200mg | Tablet | 60’s | Aurobindo Pharma | Simba Pharma |
Nevirapine | 50mg/5mL | Suspension | 240mL | Aurobindo Pharma | Simba Pharma |
Neviriv | 200mg | Tablet | 60’s | Cosmos Ltd | Cosmos Ltd |