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Aponvie Side Effects

Generic name: aprepitant

Medically reviewed by Drugs.com. Last updated on Sep 6, 2023.

Note: This document contains side effect information about aprepitant. Some dosage forms listed on this page may not apply to the brand name Aponvie.

Applies to aprepitant: oral capsule, oral powder for suspension. Other dosage forms:

Serious side effects of Aponvie

Along with its needed effects, aprepitant (the active ingredient contained in Aponvie) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor immediately if any of the following side effects occur while taking aprepitant:

Less common

Incidence not known

Other side effects of Aponvie

Some side effects of aprepitant may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common

Less common

For Healthcare Professionals

Applies to aprepitant: intravenous emulsion, oral capsule, oral kit, oral powder for reconstitution.

General

The most commonly reported side effects included headache, fatigue, neutropenia, constipation, and pruritus.[Ref]

Other

Very common (10% or more): Fatigue (up to 15%)

Common (1% to 10%): Asthenia, extremity pain, pyrexia

Uncommon (0.1% to 1%): Malaise

Rare (0.01% to 0.1%): Tinnitus

Frequency not reported: Hypothermia, pain[Ref]

Hematologic

Very common (10% or more): Neutropenia (up to 13%)

Common (1% to 10%): Anemia, hemoglobin decreased, leukopenia, white blood cell count decreased

Uncommon (0.1% to 1%): Febrile neutropenia, thrombocytopenia

Rare (0.01% to 0.1%): Neutrophil count decreased

Frequency not reported: Blood albumin decreased[Ref]

Gastrointestinal

Very common (10% or more): Diarrhea (up to 13%)

Common (1% to 10%): Abdominal pain, constipation, dyspepsia, eructation, flatulence, nausea, vomiting

Uncommon (0.1% to 1%): Dry mouth, gastritis, gastroesophageal reflux disease, oral candidiasis

Rare (0.01% to 0.1%): Abdominal distention, duodenal ulcer perforation, feces hard, neutropenic colitis, stomatitis

Frequency not reported: Abdominal pain upper, acid reflux, bowel sounds abnormal, epigastric discomfort, obstipation, stomach discomfort, subileus[Ref]

Local

Common (1% to 10%): Infusion-site erythema, infusion-site induration, infusion-site pain, infusion-site pruritus, infusion-site thrombophlebitis

Uncommon (0.1% to 1%): injection-site pain, vessel puncture-site pain[Ref]

Cardiovascular

Common (1% to 10%): Bradycardia, flushing, hypertension, hypotension

Uncommon (0.1% to 1%): Edema peripheral, flushing, hot flush, palpitations

Rare (0.01% to 0.1%): Cardiovascular disorder, chest discomfort, edema

Frequency not reported: Blood pressure decreased, hematoma, operative hemorrhage[Ref]

Nervous system

Common (1% to 10%): Dizziness, headache, peripheral neuropathy

Uncommon (0.1% to 1%): Dysgeusia, somnolence

Rare (0.01% to 0.1%): Cognitive disorder, gait disturbance, lethargy

Frequency not reported: Hypoesthesia, sensory disturbance, syncope

Postmarketing reports: Ifosfamide-induced neurotoxicity[Ref]

Hepatic

Common (1% to 10%): ALT increased, AST increased

Uncommon (0.1% to 1%): Blood alkaline phosphatase increased

Frequency not reported: Blood bilirubin increased/bilirubin increased[Ref]

Respiratory

Common (1% to 10%): Cough, hiccups

Uncommon (0.1% to 1%): Dyspnea, oropharyngeal pain, pharyngitis

Rare (0.01% to 0.1%): Postnasal drip, sneezing, throat irritation

Frequency not reported: Hypoxia, respiratory depression, wheezing[Ref]

Metabolic

Common (1% to 10%): Decreased appetite, dehydration

Uncommon (0.1% to 1%): Blood potassium decreased/hypokalemia

Rare (0.01% to 0.1%): Blood sodium decreased/hyponatremia, polydipsia, weight decreased

Frequency not reported: Blood glucose increased/hyperglycemia, hypovolemia, thirst, weight gain[Ref]

Dermatologic

Common (1% to 10%): Pruritus

Uncommon (0.1% to 1%): Acne, alopecia, hyperhidrosis, rash

Rare (0.01% to 0.1%): Photosensitivity reaction, rash pruritic, seborrhea, skin lesion, Stevens-Johnson syndrome, toxic epidermal necrolysis

Frequency not reported: Oily skin, urticaria[Ref]

Psychiatric

Common (1% to 10%): Insomnia

Uncommon (0.1% to 1%): Anxiety

Rare (0.01% to 0.1%): Abnormal behavior, agitation, behavior changes, disorientation, euphoria/euphoric mood

Frequency not reported: Dream abnormality[Ref]

Genitourinary

Common (1% to 10%): Urinary tract infection

Uncommon (0.1% to 1%): Dysuria, proteinuria

Rare (0.01% to 0.1%): Pollakiuria, red blood cells urine positive, urine output increased

Frequency not reported: Microscopic hematuria, polyuria[Ref]

Musculoskeletal

Uncommon (0.1% to 1%): Musculoskeletal pain

Rare (0.01% to 0.1%): Muscular weakness, muscle spasms

Frequency not reported: Dysarthria, muscle cramp, myalgia[Ref]

Renal

Uncommon (0.1% to 1%): Blood urea increased

Rare (0.01% to 0.1%): Glucose urine present[Ref]

Immunologic

Rare (0.01% to 0.1%): Candidiasis, staphylococcal infection

Frequency not reported: Postoperative infection, wound dehiscence[Ref]

Ocular

Rare (0.01% to 0.1%): Conjunctivitis

Frequency not reported: Miosis, visual acuity reduced[Ref]

Hypersensitivity

Frequency not reported: Anaphylactic reactions, angioedema, hypersensitivity reactions

Postmarketing reports: Anaphylactic shock, anaphylaxis[Ref]

Frequently asked questions

References

1. Product Information. Emend (aprepitant). Merck & Co., Inc. 2003.

2. Cerner Multum, Inc. UK Summary of Product Characteristics.

3. Cerner Multum, Inc. Australian Product Information.

4. Product Information. Cinvanti (aprepitant). Heron Therapeutics. 2019.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.