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Zofran (Ondansetron) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (5)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Zofran (Ondansetron) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Zofran side effects in 4 month old male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-25

Patient: 4 month old male

Reactions: Death

Adverse event resulted in: death, life threatening event, disablity

Drug(s) suspected as cause:
Zofran

Other drugs received by patient: NO Concurrent Medications



Possible Zofran side effects in 3 year old female

Reported by a physician from United States on 2012-04-27

Patient: 3 year old female, weighing 14.5 kg (31.9 pounds)

Reactions: Convulsion

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Zofran
    Indication: Prophylaxis of Nausea and Vomiting
    Start date: 2011-12-25

Zofran
    Administration route: Oral
    Start date: 2011-12-28

Other drugs received by patient: NO Concurrent Medication



Possible Zofran side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-01-24

Patient: female, weighing 72.7 kg (159.9 pounds)

Reactions: Coma, Memory Impairment, Cardiac Arrest, Deep Vein Thrombosis

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Zofran



Possible Zofran side effects in 13 year old male

Reported by a consumer/non-health professional from United States on 2011-12-01

Patient: 13 year old male, weighing 40.8 kg (89.8 pounds)

Reactions: Self Esteem Decreased, Dystonia, Neck Pain, TIC

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Zofran



Possible Zofran side effects in 71 year old male

Reported by a physician from United States on 2011-10-20

Patient: 71 year old male

Reactions: Dyspnoea, Hyperkalaemia, Atrial Fibrillation, Encephalopathy, Somnolence, Pulmonary Oedema, Renal Failure Acute, Deep Vein Thrombosis

Adverse event resulted in: death, life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Nexavar
    Administration route: Oral
    Indication: Hepatic Neoplasm Malignant
    Start date: 2009-11-02
    End date: 2009-11-08

Nexavar
    Administration route: Oral
    Start date: 2009-11-09
    End date: 2010-01-15

Zofran
    Dosage: 4-8 mg, prn
    Start date: 2010-01-06
    End date: 2010-01-29

Other drugs received by patient: Procrit; Inderal LA; Torsemide; Imodium; Lactulose; Spironolactone; Allopurinol; Rifaximin; Lactulose; Prevacid; Allopurinol; Multi-Vitamin; Folic Acid

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