Medicine details

ImageAvifanz
NameAvifanz
DosageTablet
Generic NameEfavirenz
Classes Antiinfective Agent
Antiviral Agent
NNRTI
Diseases HIV
Viral Infection
CompanyBeximco Pharmaceuticals Ltd.

Drug Package Details

Strength600 mg
Storage Condition
Origin CountryBangladesh
Commercial Pack10
Price per pack2,000.05
Cost per pack1,760.05
Package unit10 tabs strip
Price per unit200.01
Cost per unit176.00
Discount0
Coupon
Remarks

Efavirenz

Efavirenz is an anti-HIV drug from the class non nucleoside reverse transcriptase inhibitor. Efavirenz binds directly to reverse transcriptase (RT) and disrupts the enzyme's catalytic site, preventing RNA-dependent and DNA-dependent DNA polymerase activities.

Efavirenz is indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1 infection.

  • Efavirenz should be taken once daily on an empty stomach, preferably before going to bed.
  • Recommended adult dose: 600 mg.
  • Increase the voriconazole maintenance dose to 400 mg every 12 hours and reduce the Efavirenz dose to 300 mg once daily when using the capsule formulation.
  • Pediatric dosage-
    • 10 to less than 15 kg : 200 mg
    • 15 to less than 20kg : 250 mg
    • 20 to less than 25kg : 300 mg
    • 25 to less than 32.5 kg : 350mg
    • 32.5 to less than 40 kg : 400 mg
    • At least 40 kg : 600  mg

Most common adverse reactions (>5%, moderate-severe) are

  • rash
  • dizziness
  • nausea
  • headache
  • fatigue
  • insomnia
  • vomiting
  • Do not use as a single agent or add on as a sole agent to a failing regimen. Consider potential for cross resistance when choosing other agents. 
  • Not recommended with efavirenz / emtricitabine / tenofovir.
  • Serious psychiatric symptoms: Immediate medical evaluation is recommended for serious psychiatric symptoms such as severe depression or suicidal ideation
  • Nervous system symptoms (NSS): NSS are frequent, usually begin 1-2 days after initiating therapy and resolve in 2-4 weeks. Dosing at bedtime may improve tolerability. NSS are not predictive of onset of psychiatric symptoms.
  • Pregnancy: Fetal harm can occur when administered to a pregnant woman during the first trimester. Women should be apprised of the potential harm to the fetus.
  • Hepatotoxicity: Monitor liver function tests before and during treatment in patients with underlying hepatic disease, including hepatitis B or C coinfection, marked transaminase elevations, or who are taking medications associated with liver toxicity. Among reported cases of hepatic failure, a few occurred in patients with no pre-existing hepatic disease.
  • Rash: Rash usually begins within 1-2 weeks after initiating therapy and resolves within 4 weeks. Discontinue if severe rash develops.
  • Convulsions: Use caution in patients with a history of seizures.
  • Lipids: Total cholesterol and triglyceride elevations. Monitor before therapy and periodically thereafter.
  • Immune reconstitution syndrome: May necessitate further evaluation and treatment. 
  • Redistribution/accumulation of body fat: Observed in patients receiving antiretroviral therapy.

Contraindication

  • Efavirenz is contraindicated in patients with previously demonstrated hypersensitivity (eg, Stevens-Johnson syndrome, erythema multiforme, or toxic skin eruptions) to any of the components of this product.
  • For some drugs, competition for CYP3A by efavirenz could result in inhibition of their metabolism and create the potential for serious and/or life-threatening adverse reactions (eg, cardiac arrhythmias, prolonged sedation, or respiratory depression).