Anzemet Injection Side Effects
Please note - some side effects for Anzemet Injection may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA.
Side Effects by Body System - for Healthcare Professionals
Applies to: intravenous solution; oral tablet
In general, side effects have included fever (4.3%), fatigue (3.6%), pain (2.4%), and chills/shivering (2.0%).
In some controlled clinical trials, dolasetron was tested for use in the prevention of nausea and vomiting associated with moderately-emetogenic cancer chemotherapy (CINV). Patients in these trials primarily received concurrent high-dose cisplatin. In other controlled trials, dolasetron was tested for use patients for the prevention or treatment of postoperative nausea and vomiting (PONV). For many of the effects listed below, whether the patient received concurrent chemotherapy was not specified in the literature.
Nervous system side effects including headaches (9.4% to 24.3%), lightheadedness (13%), and dizziness (2.2% to 5.5%) have been reported. Flushing, vertigo, paresthesia, and tremor have been reported infrequently. Ataxia and twitching have been reported rarely.
Gastrointestinal side effects have included appetite (12% to 26.6%), diarrhea (6.0% to 12.4%), nausea (6.3% to 7%), abdominal pain (3.2%), and constipation (3.2%). Dyspepsia, abdominal pain, and anorexia have been reported infrequently. Pancreatitis has also been reported rarely.
Increases in AST and ALT did not appear to be related to dose or duration of therapy, and were not associated with symptomatic hepatic disease.
Hepatic side effects have included abnormal hepatic function (3.6%) including transient increases in AST (SGOT) and/or ALT (SGPT) (less than 1%). Hyperbilirubinemia and increased GGT have been reported rarely.
Cardiovascular side effects have rarely included hypotension, edema, peripheral edema, Mobitz I AV block, chest pain, orthostatic hypotension, myocardial ischemia, syncope, severe bradycardia, palpitations, bradycardia, tachycardia, T wave change, ST-T wave change, sinus arrhythmia, extrasystole, poor R wave progression, bundle branch block, nodal arrhythmia, U wave change, atrial flutter/fibrillation, peripheral ischemia, and thrombophlebitis/phlebitis. Rarely, cases of sustained supraventricular and ventricular arrhythmias, cardiac arrest leading to death, and myocardial infarction have been reported during postmarketing experience.
Similarly, results of a review of the cardiovascular effects of the drug class 5-hydroxytryptamine 3 receptor antagonists in the literature reported that electrocardiographic (ECG) changes were so small to be considered clinically insignificant. ECG changes were most noticeable between 1 to 2 hours after a dose of dolasetron and returned to baseline within 24 hours. To date, no serious cardiac side effects (including torsades de pointes) triggered by ECG interval changes have been connected with the use of 5-HT 3 receptor antagonists.
Dermatologic side effects have rarely included rash and increased sweating.
Ocular side effects have included blurred vision (6.3%), visual disturbance (3.2%), and photophobia (1.6%).
Hematologic side effects have included hematuria, epistaxis, prolonged prothrombin time, increased PTT, anemia, purpura/hematoma, and thrombocytopenia.
Hypersensitivity side effects have rarely included anaphylactic reaction, facial edema, and urticaria.
Metabolic side effects have rarely included increased alkaline phosphatase.
Musculoskeletal side effects have rarely included myalgia and arthralgia.
Psychiatric side effects have rarely included nervousness (3.2%). Agitation, sleep disorder, and depersonalization have been reported infrequently. Confusion, anxiety, and abnormal dreaming have been reported rarely.
Respiratory side effects have rarely included dyspnea and bronchospasm.
Genitourinary side effects have rarely included dysuria and polyuria.
Renal side effects including acute renal failure have been reported.
Other side effects including taste perversion have been reported infrequently. Tinnitus has been reported rarely.Top
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