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Pharmacologic class: Nonnucleoside reverse transcriptase inhibitor (NNRTI)

Therapeutic class: Antiretroviral

Pregnancy risk category B


Blocks human immunodeficiency virus (HIV) reverse transcriptase, an enzyme necessary for HIV replication. Blockade leads to reduced viral load and increased CD4+ cell count, which in turn help prevent other infections when drug is given with other antiretrovirals.


Tablets: 25 mg, 100 mg, 200 mg

Indications and dosages

HIV-1 infection in antiretroviral treatment-experienced patients age 6 and older who have evidence of viral replication and HIV-1 strains resistant to an NNRTI and other antiretrovirals, given in combination with other antiretrovirals

Adults and children ages 6 to younger than 18 weighing 30 kg (66 lb) or more: 200 mg P.O. b.i.d.

Children ages 6 to younger than 18 weighing 25 kg (55 lb) to less than 30 kg: 150 mg P.O. b.i.d.

Children ages 6 to younger than 18 weighing 20 kg (44 lb) to less than 25 kg: 125 mg P.O. b.i.d.

Children ages 6 to younger than 18 weighing 16 kg (35 lb) to less than 20 kg: 100 mg P.O. b.i.d.

Children's dosages shouldn't exceed the recommended adult dosage.




Use cautiously in:

• elderly patients

• pregnant or breastfeeding patients

• children younger than age 6 (safety and efficacy not established).


• Administer after a meal.

Don't give with tipranavir/ritonavir, fosamprenavir/ritonavir, atazanavir/ritonavir, protease inhibitors administered without ritonavir, other NNRTIs, or St. John's wort.

Adverse reactions

CNS: paresthesia, somnolence, seizure, hypoesthesia, amnesia, hypersomnia, tremor, disorientation, insomnia, anxiety, sleep disorder, abnormal dreams, confusional state, nervousness, nightmares, fatigue, peripheral neuropathy, headache, hemorrhagic stroke

CV: syncope, angina pectoris, hypertension, myocardial infarction, atrial fibrillation

EENT: blurred vision, vertigo

GI: nausea, vomiting, diarrhea, constipation, abdominal pain, gastroesophageal reflux disease, flatulence, gastritis, abdominal distention, retching, hematemesis, stomatitis, pancreatitis, anorexia, dry mouth

GU: gynecomastia, renal failure

Hematologic: anemia, hemolytic anemia

Hepatic: cytolytic hepatitis, hepatic steatosis, hepatitis, hepatomegaly

Metabolic: diabetes mellitus, dyslipidemia, body fat redistribution or accumulation

Respiratory: exertional dyspnea, bronchospasm

Skin: rash, hyperhidrosis, prurigo, dry skin, lipohypertrophy, lipodystrophy,

Stevens-Johnson syndrome, erythema multiforme

Other: sluggishness, night sweats, facial edema, immune reconstitution syndrome, hypersensitivity reaction, angioneurotic edema


Drug-drug. Amiodarone, bepridil, disopyramide, flecainide, lidocaine (systemic), lovastatin, mexiletine, propafenone, quinidine, simvastatin: decreased blood levels of these drugs Atazanavir/ritonavir: significant decrease in atazanavir blood level with loss of atazanavir therapeutic effect

Atorvastatin: possible increase in effects of both drugs

Carbamazepine, dexamethasone (systemic), efavirenz, nevirapine, phenobarbital, phenytoin, rifabutin, rifampin, rifapentine, ritonavir, tipranavir/ritonavir: significant decrease in etravirine blood level and loss of therapeutic effect

Clarithromycin: decreased clarithromycin blood level

Diazepam, fluvastatin, voriconazole, warfarin: increased blood levels of these drugs

Fluconazole, lopinavir/ritonavir, posaconazole: increased etravirine blood level

Immunosuppressants (cyclosporine, sirolimus, tacrolimus): possible change in blood levels of these drugs

Itraconazole, ketoconazole: decreased blood levels of these drugs, increased etravirine blood level

Methadone: possible change in methadone effects

Protease inhibitors (amprenavir, atazanavir, indinavir, nelfinavir) given without low-dose ritonavir: significant change in blood levels of these drugs

Saquinavir/ritonavir: reduced etravirine blood level

Sildenafil: possible decrease in sildenafil effect

Drug-diagnostic tests. ALP, amylase, AST, cholesterol, creatinine, glucose, lipase, low-density lipoproteins, triglycerides: increased levels

Hemoglobin, neutrophils, platelets: decreased levels

Drug-food. Any food: increased etravirine levels

Drug-herbs. St. John's wort: significant decrease in etravirine blood level and loss of therapeutic effect

Patient monitoring

Monitor patient closely for rash; discontinue therapy if severe rash develops.

• Be aware that immune reconstitution syndrome may occur in patients receiving combination antiretroviral therapy. During initial phase of therapy, patient whose immune system responds may develop inflammatory response to indolent or residual opportunistic infections (such as Mycobacterium avium complex, cytomegalovirus, Pneumocystis jiroveci pneumonia, and tuberculosis), which may necessitate further evaluation and treatment.

• Monitor International Normalized Ratio when giving drug concomitantly with warfarin.

• Watch for new-onset diabetes mellitus, exacerbation of preexisting diabetes, and hyperglycemia.

Patient teaching

• Tell patient to take drug after a meal exactly as prescribed.

• Instruct patient unable to swallow tablets whole to disperse tablets in glass of water, stir dispersion well, drink it immediately, then rinse glass with water several times and completely swallow each rinse to ensure that entire dose is consumed.

• Inform patient that drug doesn't cure HIV infection or reduce risk of passing HIV to others through sexual contact, needle sharing, or blood exposure.

• Advise patient that drug may interact with many other drugs and herbs (especially St. John's wort). Tell patient to discuss use of other drugs and herbs with prescriber.

Advise patient to immediately report rash or new infections.

• Inform patient that drug may lead to body fat redistribution or accumulation and that the cause and long-term effects of these conditions are unknown.

• Advise female patient to notify prescriber if she is pregnant or intends to become pregnant.

• Because of potential HIV transmission and adverse reactions in breastfeeding infants, instruct women receiving this drug not to breastfeed.

• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, foods, and herbs mentioned above.

McGraw-Hill Nurse's Drug Handbook, 7th Ed. Copyright © 2013 by The McGraw-Hill Companies, Inc. All rights reserved


(e-tra-veer-een) ,


(trade name)


Therapeutic: antiretrovirals
Pharmacologic: non nucleoside reverse transcriptase inhibitors
Pregnancy Category: B


HIV-1 infection (with other antiretrovirals) in treatment-experienced patients who have evidence of viral replication and HIV-1 strains resistant to a non-nucloside reverse transcriptase inhibitor (NNRTI) and other antiretrovirals.


Binds to the enzyme reverse transcriptase, which results in disrupted viral DNA synthesis.

Therapeutic effects

Evidence of decreased viral replication and reduced viral load with slowed progression of HIV and its sequelae.


Absorption: Well absorbed following oral administration. Food enhances absorption.
Distribution: Unknown.
Protein Binding: 99.9%.
Metabolism and Excretion: Mostly metabolized by the liver (CYP3A4, CYP2C9, and CYP2C19 enzyme systems); minimal renal excretion; mostly eliminated in feces as unchanged drug and metabolites.
Half-life: 41 hr.

Time/action profile (blood levels)

POunknown2.5–4 hr12 hr


Contraindicated in: Concurrent use with other NNRTIs, rifampin, rifapentine, St. John's wort.
Use Cautiously in: Concurrent use of antiarrhythmics, anticonvulsants, antifungals, clarithyromycin, rifabutin, diazepam, dexamethasone, HMG CoA reductase inhibitors (statins), immunosuppressants; Geriatric: Consider age-related ↓ in organ function and body mass, concurrent disease states and medications; Obstetric / Lactation: Safety not established, breast feeding not recommended in HIV-infected women Pediatric: Children <6 yr (safety not established)

Adverse Reactions/Side Effects

Central nervous system

  • seizures (life-threatening)
  • anxiety
  • confusion
  • fatigue
  • headache
  • insomnia
  • sleep disorders

Ear, Eye, Nose, Throat

  • blurred vision
  • vertigo


  • myocardial infarction (life-threatening)
  • angina pectoris
  • atrial fibrillation
  • hypertension


  • hepatic failure (life-threatening)
  • nausea (most frequent)
  • abdominal pain
  • anorexia
  • dry mouth
  • hepatitis
  • stomatitis
  • vomiting


  • renal failure


  • gynecomastia
  • hyperglycemia
  • hyperlipidemia


  • anemia
  • hemolytic anemia


  • erythema multiforme (life-threatening)
  • stevens-johnson syndrome (life-threatening)
  • toxic epidermal necrolysis (life-threatening)
  • rash (most frequent)


  • fat redistribution


  • peripheral neuropathy


  • hemarthrosis


  • drug rash with eosinophilia and systemic symptoms (dress) (life-threatening)
  • immune reconstitution syndrome


Drug-Drug interaction

Etravirine is a substrate of the CYP3A4, CYP2C9, and CYP2C19 enzyme systems; other medications that induce or inhibit these systems may be expected to alter the response to etravirine. Etravirine is an inducer of CYP3A4 and an inhibitor of CYP2C9 and CYP2C19. The effects of medications that are substrates of these enzyme systems may be altered by concurrent use.Concurrent use with other NNRTIs including efavirenz, nevirapine, rilpivirine, and delavirdine may lead to ↓ effectiveness and should be avoided.Concurrent use with protease inhibitors (PIs), including nelfinavir and indinavir, may lead to altered plasma levels and should be untertaken with concurrent low dose ritonavir.Concurrent use with higher dose ritonavir, combination tipranavir/ritonavir, fosamprenavir/ritonavir, and atazanavir/ritonavir alter levels and effectiveness of etravirine and should be avoided.Concurrent use with lopinavir/ritonavir may ↓ levels.Concurrent use of the combination saquinavir/ritonavir should be undertake cautiously.↓ blood levels and effectiveness of antiarrhythmics including amiodarone, disopyramide, flecainide, lidocaine, mexiletine, quinidine, propafenone, and quinidine ; blood level monitoring recommended.Blood levels and effects may be ↓ by anticonvulsants including carbamazepine, phenobarbital, and phenytoin.Concurrent use with voriconazole may ↑ levels of both drugs; ↓ levels of itraconazole and ketoconazole (dose adjustments may be necessary).Concurrent use with fluconazole may ↑ levels.May alter levels and response to clarithromycin ; other agents should be considered.Rifampin and rifapentine ↓ blood levels and effectiveness and should be avoided; rifabutin should only be used without a protease inhibitor/ritonavir combination.May ↑ blood levels and sedation from diazepam ; monitor for effects.Levels and effectiveness may be ↓ by dexamethasone ; use cautiously and consider alternatives.May alter blood levels and effects of fluvastatin, lovastatin, and simvastatin (dose adjustments may be necessary.May alter blood levels and effects of cyclosporine, sirolimus, and tacrolimus ; careful monitoring required.May ↓ the antiplatelet effects of clopidogrel.May ↓ buprenorphine levels.May ↓ levels of artemether/lumefantrine and telaprevir St. John's wort may ↓ blood levels and effectiveness; avoid concurrent use.


Oral (Adults) 200 mg twice daily.
Oral (Children 6–17 yr and ≥30 kg) 200 mg twice daily
Oral (Children 6–17 yr and 25–29 kg) 150 mg twice daily
Oral (Children 6–17 yr and 20–24 kg) 125 mg twice daily
Oral (Children 6–17 yr and 16–19 kg) 100 mg twice daily


Tablets: 25 mg, 100 mg, 200 mg

Nursing implications

Nursing assessment

  • Assess for change in severity of HIV symptoms and for symptoms of opportunistic infections during therapy.
  • Assess patient for rash (mild to moderate rash usually occurs in the 2nd wk of therapy and resolves within 1–2 wk of continued therapy). If rash is severe (extensive erythematous or maculopapular rash with moist desquamation or angioedema) or accompanied by systemic symptoms (serum sickness-like reaction, Stevens-Johnson syndrome, toxic epidermal necrolysis), therapy must be discontinued immediately.
  • Lab Test Considerations: Monitor viral load and CD4 cell count regularly during therapy.
    • Monitor liver function tests periodically during therapy. May cause ↑ serum AST, ALT concentrations.
    • May cause ↑ pancreatic amylase and lipase.
    • May cause ↑ in total cholesterol, low density lipoprotein, serum triglyceride, and glucose levels.
    • May cause ↑ serum creatinine.
    • May cause ↓ neutrophils, ↓ platelet count, anemia and hemolytic anemia.

Potential Nursing Diagnoses

Risk for infection (Indications)
Noncompliance (Patient/Family Teaching)


  • Oral: Administer tablets twice daily following a meal; type of food does not matter. Swallow tablet whole; do not break, crush, or chew. If patient has difficulty swallowing, may disperse tablet in 5 mL (1 tsp) of water, or at least enough liquid to cover the medication; stir well until water looks milky. Add more water or orange juice or milk (do not place tablets in orange juice or milk without first adding water). Avoid grapefruit juice, warm, or carbonated beverages. Once dispersed, patient should stir well and drink immediately; rinse glass with water and drink several times to ensure entire dose is consumed.

Patient/Family Teaching

  • Emphasize the importance of taking etravirine as directed, at the same time each day. 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 following a meal if remembered within 6 hr of the time it is usually taken, then return to regular schedule. If more than 6 hr from time dose is usually taken, omit dose and resume dosing schedule; do not double doses.
  • Instruct patient that etravirine should not be shared with others.
  • Inform patient that etravirine does not cure AIDS or prevent associated or opportunistic infections. Etravirine does not 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 etravirine are unknown at this time.
  • 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, signs of hypersensitivity (fever, generally ill feeling, extreme tiredness, muscle or joint aches, blisters, oral lesions, eye inflammation, facial swelling), signs and symptoms of liver problems (yellowing of skin or whites of eyes, dark or tea colored urine, pale-colored stools/bowel movements, nausea, vomiting, loss of appetite, or pain, aching, or sensitivity on right side below ribs), or signs of Immune Reconstitution Syndrome (signs and symptoms of an infection) occur.
  • Advise 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, especially St. John's wort.
  • Inform patient that changes in body fat (increased fat in upper back and neck, breast, and around back, chest, and stomach area; loss of fat from legs, arms, and face) may occur.
  • Advise patients taking oral contraceptives to use a nonhormonal method of birth control during etravirine therapy and to notify health care professional if they become pregnant or plan to breast feed while taking etravirine.
  • 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.
Drug Guide, © 2015 Farlex and Partners
References in periodicals archive ?
The marketed drug product Intelence is an example of an SDD incorporated into a tablet at a 100 mg active dosage strength.
(16.) Intelence [package insert], Titusville, NJ: Tibotec Pharmaceuticals; 2014.
Miralles joined Johnson and Johnson as VP of Clinical Development at Tibotec in Belgium, where he was involved in the development and approval of several drugs including PREZISTA and INTELENCE.
Market Access Impact: HIV explores how cost concerns and other barriers affect market share for 8 major HIV treatments: Celsentri, Evotaz, Intelence, Isentress, Stribild, Triumeq, Truvada, and Viread.
(1) Viral load control rates did not differ significantly in people taking a combination including a nonnucleoside (like Edurant, Intelence, or Sustiva) if their pill-taking on-time record lay between 90% and 94% or at 95% or greater.
Together, they control a significant portion of the AIDS drug market with drugs that include Prezista, Intelence, Endurant and Procrit.
They include delavirdine (Rescriptor), efavirenz (Sustiva, Stocrin), nevirapine (Viramune) and etravirine (Intelence).
The most common regimen (56%) was raltegravir (Isentress), darunavir/ritonavir (Prezista), and the NNRTI etravirine (Intelence), said Dr.
Johnson & Johnson's (New Brunswick NJ) Tibotec Therapeutics unit won approval for its Intelence HIV drug designed to treat patients who have stopped responding to other treatments.
Etravirine, a nonnucleoside reverse transcriptase inhibitor marketed as Intelence, was approved in January 2008 for use in combination with other antiretrovirals for treating HIV-1 infection in treatment-experienced adults.
Etravirine (Intelence; Tibotec), a second-generation NNRTI, requires multiple mutations, and is effective in treating most patients who have failed efavirenz or nevirapine.