Anzemet Injection
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Anzemet Injection
Anzemet Injection Side Effects Center
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
Anzemet Injection FDA Prescribing Information: Side Effects
(Adverse Reactions)
SIDE EFFECTS
Chemotherapy Patients
In controlled clinical trials, 2265 adult patients received ANZEMET Injection (dolasetron mesylate injection) . The overall adverse event rates were similar with 1.8 mg/kg ANZEMET Injection (dolasetron mesylate injection) and ondansetron or granisetron. Patients were receiving concurrent chemotherapy, predominantly high-dose (≥ 50 mg/m2) cisplatin. Following is a combined listing of all adverse events reported in ≥ 2% of patients in these controlled trials (Table 4).
TABLE 4. ADVERSE EVENTS ≥ 2% FROM CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING STUDIES
| Event | ANZEMET Injection (dolasetron mesylate injection) 1.8 mg/kg (n=695) |
Ondansetron/ Granisetron* (n=356) |
||
| Headache | 169 | (24.3%) | 73 | (20.5%) |
| Diarrhea | 86 | (12.4%) | 25 | (7.0%) |
| Fever | 30 | (4.3%) | 18 | (5.1%) |
| Fatigue | 25 | (3.6%) | 12 | (3.4%) |
| Hepatic Function Abnorma† | 25 | (3.6%) | 12 | (3.4%) |
| Abdominal Pain | 22 | (3.2%) | 7 | (2.0%) |
| Hypertension | 20 | (2.9%) | 9 | (2.5%) |
| Pain | 17 | (2.4%) | 7 | (2.0%) |
| Dizziness | 15 | (2.2%) | 7 | (2.0%) |
| Chills/Shivering | 14 | (2.0%) | 6 | (1.7%) |
| *: Ondansetron 32 mg intravenous, granisetron 3 mg intravenous.
† : Includes events coded as SGOT- and/or SGPT-increased (see also Liver and Biliary System below) |
||||
Postoperative Patients
In controlled clinical trials with 2550 adult patients, headache and dizziness were reported more frequently with 12.5 mg ANZEMET Injection (dolasetron mesylate injection) than with placebo. Rates of other adverse events were similar. Following is a listing of all adverse events reported in ≥ 2% of patients receiving either placebo or 12.5 mg ANZEMET Injection (dolasetron mesylate injection) for the prevention or treatment of postoperative nausea and vomiting in controlled clinical trials (Table 5).
Table 5. Adverse Events ≥ 2% from Placebo-Controlled Postoperative Nausea and Vomiting Studies
| Event | ANZEMET Injection (dolasetron mesylate injection) 12.5 mg (n=615) |
Placebo (n=739) |
| Headache | 58 (9.4%) | 51 (6.9%) |
| Dizziness | 34 (5.5%) | 23 (3.1%) |
| Drowsiness | 15 (2.4%) | 18 (2.4%) |
| Pain | 15 (2.4%) | 21 (2.8%) |
| Urinary Retention | 12 (2.0%) | 16 (2.2%) |
In clinical trials, the following infrequently reported adverse events, assessed by investigators as treatment-related or causality unknown, occurred following oral or intravenous administration of ANZEMET to adult patients receiving concomitant cancer chemotherapy or surgery:
Cardiovascular: Hypotension; rarely - edema, peripheral edema. The following events also occurred rarely and with a similar frequency as placebo and/or active comparator: Mobitz I AV block, chest pain, orthostatic hypotension, myocardial ischemia, syncope, severe bradycardia, and palpitations. See PRECAUTIONS section for information on potential effects on ECG.
In addition, the following asymptomatic treatment-emergent ECG changes were seen at rates less than or equal to those for active or placebo controls: bradycardia, tachycardia, T wave change, ST-T wave change, sinus arrhythmia, extrasystole (APCs or VPCs), poor R-wave progression, bundle branch block (left and right), nodal arrhythmia, U wave change, atrial flutter/fibrillation.
Furthermore, severe hypotension, bradycardia and syncope have been reported immediately or closely following IV administration.
Dermatologic: Rash, increased sweating.
Gastrointestinal System: Constipation, dyspepsia, abdominal pain, anorexia; rarely - pancreatitis.
Hearing, Taste and Vision: Taste perversion, abnormal vision; rarely - tinnitus, photophobia.
Hematologic: Rarely - hematuria, epistaxis, prothrombin time prolonged, PTT increased, anemia, purpura/hematoma, thrombocytopenia.
Hypersensitivity: Rarely - anaphylactic reaction, facial edema, urticaria.
Liver and Biliary System: Transient increases in AST (SGOT) and/or ALT (SGPT) values have been reported as adverse events in less than 1% of adult patients receiving ANZEMET in clinical trials. The increases did not appear to be related to dose or duration of therapy and were not associated with symptomatic hepatic disease. Similar increases were seen with patients receiving active comparator. Rarely - hyperbilirubinemia, increased GGT.
Metabolic and Nutritional: Rarely - alkaline phosphatase increased.
Musculoskeletal: Rarely - myalgia, arthralgia.
Nervous System: Flushing, vertigo, paraesthesia, tremor; rarely - ataxia, twitching. Psychiatric: Agitation, sleep disorder, depersonalization; rarely - confusion, anxiety, abnormal dreaming.
Respiratory System: Rarely - dyspnea, bronchospasm.
Urinary System: Rarely - dysuria, polyuria, acute renal failure.
Vascular (Extracardiac): Local pain or burning on IV administration; rarely - peripheral ischemia, thrombophlebitis/phlebitis.
Postmarketing Experience:
There are rare reports of wide complex tachycardia or ventricular tachycardia and of ventricular fibrillation cardiac arrest following intravenous administration.
Read the entire FDA prescribing information for Anzemet Injection (Dolasetron Mesylate Injection) »
Additional Anzemet Injection Information
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