Zinecard Side Effects
Generic Name: dexrazoxane
Please note - some side effects for Zinecard 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 of Zinecard - for the Consumer
Zinecard
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome when using Zinecard:
Seek medical attention right away if any of these SEVERE side effects occur when using Zinecard:Diarrhea; difficulty swallowing; fever; general body discomfort; hair loss; infection (chills; sore throat); loss of appetite; nausea; pain or swelling at the injection site; streaking or flushing of the skin; swelling of the throat or tongue; tiredness; vomiting.
Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
TopZinecard Side Effects - for the Professional
Zinecard
Zinecard at a dose of 500 mg/m2 has been administered in combination with FAC in randomized, placebo-controlled, double-blind studies to patients with metastatic breast cancer. The dose of doxorubicin was 50 mg/m2 in each of the trials. Courses were repeated every three weeks, provided recovery from toxicity had occurred. Table 3 below lists the incidence of adverse experiences for patients receiving FAC with either Zinecard or placebo in the breast cancer studies. Adverse experiences occurring during courses 1 through 6 are displayed for patients receiving Zinecard or placebo with FAC beginning with their first course of therapy (columns 1 and 3, respectively). Adverse experiences occurring at course 7 and beyond for patients who received placebo with FAC during the first six courses and who then received either Zinecard or placebo with FAC are also displayed (columns 2 and 4, respectively).
| ADVERSE EXPERIENCE | PERCENTAGE (%) OF BREAST CANCER PATIENTS WITH ADVERSE EXPERIENCE | |||
|---|---|---|---|---|
| FAC + Zinecard | FAC + PLACEBO | |||
| Courses 1– 6 N = 413 |
Courses ≥ 7 N = 102 |
Courses 1– 6 N = 458 |
Courses ≥ 7 N = 99 |
|
| Alopecia | 94 | 100 | 97 | 98 |
| Nausea | 77 | 51 | 84 | 60 |
| Vomiting | 59 | 42 | 72 | 49 |
| Fatigue/Malaise | 61 | 48 | 58 | 55 |
| Anorexia | 42 | 27 | 47 | 38 |
| Stomatitis | 34 | 26 | 41 | 28 |
| Fever | 34 | 22 | 29 | 18 |
| Infection | 23 | 19 | 18 | 21 |
| Diarrhea | 21 | 14 | 24 | 7 |
| Pain on Injection | 12 | 13 | 3 | 0 |
| Sepsis | 17 | 12 | 14 | 9 |
| Neurotoxicity | 17 | 10 | 13 | 5 |
| Streaking/Erythema | 5 | 4 | 4 | 2 |
| Phlebitis | 6 | 3 | 3 | 5 |
| Esophagitis | 6 | 3 | 7 | 4 |
| Dysphagia | 8 | 0 | 10 | 5 |
| Hemorrhage | 2 | 3 | 2 | 1 |
| Extravasation | 1 | 3 | 1 | 2 |
| Urticaria | 2 | 2 | 2 | 0 |
| Recall Skin Reaction | 1 | 1 | 2 | 0 |
The adverse experiences listed above are likely attributable to the FAC regimen with the exception of pain on injection that was observed mainly on the Zinecard arm.
Myelosuppression
Patients receiving FAC with Zinecard experienced more severe leukopenia, granulocytopenia, and thrombocytopenia at nadir than patients receiving FAC without Zinecard, but recovery counts were similar for the two groups of patients.
Hepatic and Renal
Some patients receiving FAC + Zinecard or FAC + placebo experienced marked abnormalities in hepatic or renal function tests, but the frequency and severity of abnormalities in bilirubin, alkaline phosphatase, BUN, and creatinine were similar for patients receiving FAC with or without Zinecard.
TopSide Effects by Body System - for Healthcare Professionals
Gastrointestinal
Gastrointestinal side effects including nausea (43%), vomiting (19%), diarrhea (11%), abdominal pain (6%), and constipation (6%) have been reported.
General
General side effects including pyrexia (21%), postoperative infection (16%), fatigue (13%), peripheral edema (10%), chest pain, chest discomfort, decreased drug effect, hyperpyrexia, and decreased therapeutic response have been reported.
Local
Local side effects including injection site pain (16%) and injection site phlebitis (6%) have been reported.
Cardiovascular
Cardiovascular side effects including vascular disorders (15%) and cardiac disorders (5%) have been reported.
Dermatologic
Dermatologic side effects including alopecia (14%) have been reported.
Musculoskeletal
Musculoskeletal side effects including "musculoskeletal and connective tissue disorders" (13%) have been reported.
Nervous system
Nervous system side effects including dizziness (11%) and headache (6%) have been reported.
Respiratory
Respiratory side effects including dyspnea (8%), pneumonia (6%), and cough (5%) have been reported.
Psychiatric
Psychiatric side effects including depression (8%), anorexia (5%), and insomnia (5%) have been reported.
Hematologic
Hematologic side effects including anemia (6%), decreased WBC, decreased neutrophils, and decreased platelets have been reported.
Hepatic
Hepatic side effects including increased bilirubin, increased AST, increased ALT, increased alkaline phosphatase, and increased LDH have been reported
Metabolic
Metabolic side effects including increased creatinine, decreased sodium, and increased total calcium have been reported.
TopMore Zinecard resources
- Zinecard Prescribing Information (FDA)
- Zinecard Advanced Consumer (Micromedex) - Includes Dosage Information
- Zinecard Monograph (AHFS DI)
- Zinecard MedFacts Consumer Leaflet (Wolters Kluwer)
- Dexrazoxane Prescribing Information (FDA)
- Dexrazoxane Professional Patient Advice (Wolters Kluwer)
- Totect Prescribing Information (FDA)
- Totect Consumer Overview
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