efavirenz

ROUTE	ONSET	PEAK	DURATION
PO	rapid	3–5 hr	24 hr

Contraindicated in:

Hypersensitivity;
Moderate to severe hepatic impairment.
Concurrent use of elbasvir and grazoprevir;
Lactation: Breastfeeding not recommended for women with HIV.

Use Cautiously in:

History of mental illness or substance abuse (↑ risk of psychiatric symptomatology);
Mild hepatic impairment (including coinfection with hepatitis B/C);
History of seizure disorders (↑ risk of seizures);
OB: Use in pregnancy only if other options have been exhausted; birth defects have been reported;
Pedi: Children 3 mo (safety and effectiveness not established); incidence of rash;
Geri: Use lower initial dose in older adults due to incidence of renal or cardiac dysfunction.

Adv. Reactions/Side Effects ⬆ ⬇

CV: QT interval prolongation

Derm: rash, pruritus, sweating

Endo: Graves' disease, hypercholesterolemia, hypertriglyceridemia

GI: nausea, abdominal pain, anorexia, autoimmune hepatitis, diarrhea, dyspepsia, flatulence, HEPATOTOXICITY

GU: hematuria, renal calculi

Metab: fat redistribution

MS: polymyositis

Neuro: Guillain-Barré syndrome, abnormal dreams, ataxia, catatonia, delusions, depression, dizziness, drowsiness, encephalopathy, fatigue, headache, hypoesthesia, impaired concentration, insomnia, nervousness, psychoses, SUICIDAL THOUGHTS/BEHAVIORS

Misc: immune reconstitution syndrome

Interactions ⬆ ⬇

Drug-drug:

May lead to loss of virologic response to elbasvir/grazoprevir; concurrent use contraindicated.
Induces (stimulates) the hepatic cytochrome P450 3A4 enzyme system and would be expected to influence the effects of other drugs that are metabolized by this system; efavirenz itself is also metabolized by this system.
↑risk of CNS depression with other CNS depressants, including alcohol, antidepressants, antihistamines, and opioid analgesics.
May ↓ the effectiveness of progestin-containing hormonal contraceptives (e.g., etonogestrel, norelgestromin, levonorgestrel).
Use with voriconazole significantly ↓ voriconazole levels and ↑ efavirenz levels; avoid concurrent use with standard doses of voriconazole; if used together, ↑ dose of voriconazole to 400 mg every 12 hr and ↓ dose of efavirenz to 300 mg daily.
May ↓ posaconazole levels; avoid concurrent use.
May ↓ itraconazole levels; use alternative antifungal agent.
May ↓ ketoconazole levels
May ↓ fosamprenavir levels; ↑ dose of ritonavir when given with fosamprenavir/ritonavir once daily.
May ↓ atazanavir levels; dosage adjustments may be needed in treatment-naïve patients; avoid concurrent use in treatment-experienced patients.
May ↓ lopinavir levels; ↑ dose of lopinavir/ritonavir; avoid concurrent use of lopinavir/ritonavir once daily.
May ↑ ritonavir levels; monitor liver function tests.
May ↓ raltegravir levels and effectiveness.
↓maraviroc levels; ↑ maraviroc dose.
May alter the effects of warfarin.
May ↓ levels of cyclosporine, tacrolimus, and sirolimus.
May ↓ levels of bupropion and sertraline.
Rifampin may ↓ levels; ↑ dose of efavirenz
Concurrent use with other NNRTIs including etravirine, nevirapine, and rilpivirine may lead to ↓ effectiveness and should be avoided.
May ↓ levels of raltegravir.
Concurrent use with carbamazepine may ↓ levels of carbamazepine and efavirenz; use alternative anticonvulsant agent
Concurrent use with phenytoin or phenobarbital may ↓ levels of phenytoin, carbamazepine, and efavirenz
May ↓ levels of clarithromycin; consider using azithromycin
May ↓ levels of rifabutin; ↑ daily dose of rifabutin by 50%
May ↓ levels of calcium channel blockers, atorvastatin, pravastatin, simvastatin, methadone, and artemether/lumefantrine.
May ↓ levels of progestin-containing contraceptives and etonogestrel; use reliable method of barrier contraception in addition to hormonal contraceptive agent.
Concurrent use with other QT interval prolonging medications may ↑ risk of QT interval prolongation or torsades de pointes.
May ↓ therapeutic effects of pibrentasvir/glecaprevir, velpatasvir/sofosbuvir, and velpatasivir/sofosbuvir/voxilaprevir; avoid concurrent use.

Ingestion following a high-fat meal↑ absorption by 50%.

Route/Dosage ⬆ ⬇

PO (Adults and Children ≥40 kg): 600 mg once daily; Concurrent rifampin therapy (in patients >50 kg): 800 mg once daily.
PO (Children ≥3 mo and 32.5–39.9 kg): 400 mg once daily.
PO (Children ≥3 mo and 25–32.4 kg): 350 mg once daily.
PO (Children ≥3 mo and 20–24.9 kg): 300 mg once daily.
PO (Children ≥3 mo and 15–19.9 kg): 250 mg once daily.
PO (Children ≥3 mo and 7.5–14.9 kg): 200 mg once daily.
PO (Children ≥3 mo and 5–7.4 kg): 150 mg once daily.
PO (Children ≥3 mo and 3.5–4.9 kg): 100 mg once daily.

Availability ⬆ ⬇

(Generic available)

Capsules: 50 mg; 200 mg
Tablets: 600 mg
In combination with: emtricitabine and tenofovir disoproxil fumarate (Atripla); lamivudine and tenofovir disoproxil fumarate (Symfi, Symfi Lo). (See Appendix [not included in this PDA edition]).

Assessment ⬆ ⬇

Assess for change in severity of HIV symptoms and for symptoms of opportunistic infections during therapy.
Assess for rash, especially during 1st mo of therapy. Onset is usually within 2 wk and resolves with continued therapy within 1 mo. May range from mild maculopapular with erythema and pruritus to exfoliative dermatitis and Stevens-Johnson syndrome. Occurs more often and may be more severe in children. If rash is severe or accompanied by blistering, desquamation, mucosal involvement, or fever, therapy must be discontinued immediately. Efavirenz may be reinstated concurrently with antihistamines or corticosteroids in patients discontinuing due to rash.
Assess patient for CNS and psychiatric symptoms (dizziness, impaired concentration, somnolence, abnormal dreams, insomnia, suicidal thoughts and behaviors) during therapy. Symptoms usually begin during 1st or 2nd day of therapy and resolve after 2–4 wk. Administration at bedtime may minimize symptoms. Concurrent use with alcohol or psychoactive agents may cause additive CNS symptoms.

Lab Test Considerations:

Monitor viral load and CD4 cell count regularly during therapy.
- Verify negative pregnancy test prior to starting therapy. May cause fetal harm if administered during first trimester of pregnancy.
- Monitor liver function tests before and periodically during therapy in all patients. Discontinue therapy if persistent ↑ in serum transaminases >5 x upper limit of normal (ULN) or if clinical signs and symptoms of hepatic dysfunction occur.
- May cause ↑ in total cholesterol and serum triglyceride levels.
- May cause false-positive urine cannabinoid results.

Implementation ⬆ ⬇

PO: Administer on an empty stomach, preferably at bedtime to minimize nervous system side effects. Avoid taking with a high-fat meal. DNC: Do not break tablets.
- Capsule may be opened and contents sprinkled on a small amount (1 to 2 tsp) of food for children at least 3 mo old and weighing at least 3.5 kg and adults who cannot swallow capsules or tablets. Open capsule carefully; avoid spillage or dispersion of contents into the air. For infants receiving capsule sprinkle-infant formula mixture, gently mix entire capsule contents into 2 tsp (10 mL) of reconstituted room temperature infant formula in a medicine cup, then draw up mixture into a 10 mL oral dosing syringe for administration. Use of infant formula for mixing should only be considered for those young infants who cannot consume solid foods. For patients able to tolerate solid foods, mix entire capsule contents gently with soft food (applesauce, grape jelly, yogurt). After administration of mixture, add a small amount (2 tsp) of food or formula to empty mixing container, stir to disperse any remaining efavirenz residue, and administer to patient. Administer mixture within 30 minutes of mixing. Avoid food for 2 hr after administration.

Patient/Family Teaching ⬆ ⬇

Emphasize the importance of taking efavirenz as directed. It must always be used in combination with other antiretroviral drugs. Do not take more than prescribed amount, and do not stop taking without consulting health care professional. Take missed doses as soon as remembered; do not double doses. Advise patient to read Patient Information before starting therapy and with each Rx refill in case of changes.
Instruct patient that efavirenz should not be shared with others.
May cause dizziness, impaired concentration, or drowsiness. Caution patient to avoid driving or other activities requiring alertness until response to medication is known.
Instruct patient to notify health care professional immediately if rash or suicidal thoughts or behaviors occur.
Inform patient that efavirenz does not cure AIDS or prevent associated or opportunistic infections. Efavirenz may reduce the risk of transmission of HIV to others through sexual contact or blood contamination. Caution patient to use a condom and to avoid sharing needles or donating blood to prevent spreading the AIDS virus to others. Advise patient that the long-term effects of efavirenz are unknown at this time.
Inform patient that redistribution and accumulation of body fat may occur, causing central obesity, dorsocervical fat enlargement (buffalo hump), peripheral wasting, breast enlargement, and cushingoid appearance. The cause and long-term effects are not known.
Instruct patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and to consult with health care professional before taking other medications.
Inform patient of risk of developing late-onset neurotoxicity (ataxia, encephalopathy); may occur months to years after starting therapy.
Rep: May cause fetal harm. Advise females of reproductive potential taking oral contraceptives to use a nonhormonal method of birth control during efavirenz therapy and for at least 12 wk following discontinuation and to avoid breastfeeding. Advise patient to notify health care professional if they become pregnant while taking efavirenz. Encourage patients who become pregnant during therapy to join the Antiretroviral Pregnancy Registry that monitors pregnancy outcomes in women exposed to efavirenz during pregnancy. Enroll patient by calling 1-800-258-4263.
Emphasize the importance of regular follow-up exams and blood counts to determine progress and monitor for side effects.

Evaluation/Desired Outcomes ⬆ ⬇

Delayed progression of AIDS and decreased opportunistic infections in patients with HIV.
Decrease in viral load and increase in CD4 cell counts.

Canadian Brand Names ⬆ ⬇

Code ⬆

NDC Code

0056- Bristol-Myers Squibb Pharma Company
- 0056-0470- SUSTIVA
  - 0056-0470-30- 30 CAPSULE, GELATIN COATED in 1 BOTTLE (0056-0470-30)

0056- Bristol-Myers Squibb Pharma Company
- 0056-0474- SUSTIVA
  - 0056-0474-92- 90 CAPSULE, GELATIN COATED in 1 BOTTLE (0056-0474-92)

0056- Bristol-Myers Squibb Pharma Company
- 0056-0510- SUSTIVA
  - 0056-0510-30- 30 TABLET, FILM COATED in 1 BOTTLE (0056-0510-30)

0378- Mylan Pharmaceuticals Inc.
- 0378-2233- Efavirenz
  - 0378-2233-93- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2233-93)

31722- Camber Pharmaceuticals, Inc.
- 31722-504- Efavirenz
  - 31722-504-25- 250 TABLET, FILM COATED in 1 BOTTLE (31722-504-25)

31722- Camber Pharmaceuticals, Inc.
- 31722-504- Efavirenz
  - 31722-504-30- 30 TABLET, FILM COATED in 1 BOTTLE (31722-504-30)

64380- Strides Pharma Science Limited
- 64380-889- Efavirenz
  - 64380-889-04- 30 TABLET in 1 BOTTLE (64380-889-04)

64980- Rising Pharmaceuticals, Inc.
- 64980-406- Efavirenz
  - 64980-406-03- 30 CAPSULE in 1 BOTTLE (64980-406-03)

64980- Rising Pharmaceuticals, Inc.
- 64980-407- Efavirenz
  - 64980-407-09- 90 CAPSULE in 1 BOTTLE (64980-407-09)

65862- Aurobindo Pharma Limited
- 65862-049- Efavirenz
  - 65862-049-10- 3 BLISTER PACK in 1 CARTON (65862-049-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

65862- Aurobindo Pharma Limited
- 65862-049- Efavirenz
  - 65862-049-30- 30 TABLET, FILM COATED in 1 BOTTLE (65862-049-30)

65862- Aurobindo Pharma Limited
- 65862-104- Efavirenz
  - 65862-104-10- 3 BLISTER PACK in 1 CARTON (65862-104-10) > 10 CAPSULE in 1 BLISTER PACK

65862- Aurobindo Pharma Limited
- 65862-104- Efavirenz
  - 65862-104-30- 30 CAPSULE in 1 BOTTLE (65862-104-30)

65862- Aurobindo Pharma Limited
- 65862-105- Efavirenz
  - 65862-105-10- 3 BLISTER PACK in 1 CARTON (65862-105-10) > 10 CAPSULE in 1 BLISTER PACK

65862- Aurobindo Pharma Limited
- 65862-105- Efavirenz
  - 65862-105-30- 30 CAPSULE in 1 BOTTLE (65862-105-30)

65862- Aurobindo Pharma Limited
- 65862-106- Efavirenz
  - 65862-106-09- 9 BLISTER PACK in 1 CARTON (65862-106-09) > 10 CAPSULE in 1 BLISTER PACK

65862- Aurobindo Pharma Limited
- 65862-106- Efavirenz
  - 65862-106-10- 3 BLISTER PACK in 1 CARTON (65862-106-10) > 10 CAPSULE in 1 BLISTER PACK

65862- Aurobindo Pharma Limited
- 65862-106- Efavirenz
  - 65862-106-30- 30 CAPSULE in 1 BOTTLE (65862-106-30)

65862- Aurobindo Pharma Limited
- 65862-106- Efavirenz
  - 65862-106-90- 90 CAPSULE in 1 BOTTLE (65862-106-90)

65862- Aurobindo Pharma Limited
- 65862-774- Efavirenz
  - 65862-774-30- 30 TABLET, FILM COATED in 1 BOTTLE (65862-774-30)

69097- Cipla USA Inc.
- 69097-301- Efavirenz
  - 69097-301-02- 30 TABLET, FILM COATED in 1 BOTTLE (69097-301-02)

70518- REMEDYREPACK INC.
- 70518-0482- SUSTIVA
  - 70518-0482-0- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0482-0)

70518- REMEDYREPACK INC.
- 70518-1013- Efavirenz
  - 70518-1013-0- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1013-0)

70518- REMEDYREPACK INC.
- 70518-1100- Efavirenz
  - 70518-1100-0- 30 TABLET in 1 BLISTER PACK (70518-1100-0)

section name header

Pronunciation ⬇

Classifications ⬆ ⬇

Indications ⬆ ⬇

Action ⬆ ⬇

Pharmacokinetics ⬆ ⬇

Time/Action Profile ⬆ ⬇

Contraind./Precautions ⬆ ⬇