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Index of reports
> Disability (5)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Temodar (Temozolomide) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Temodar side effects in
Reported by a physician from United States on 2012-08-14
Patient:
Reactions: Mental Status Changes, Nephrogenic Diabetes Insipidus
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Temodar
Dosage: 150 mg/m2, unk
Temodar
Dosage: 75 mg/m2, concomitantly with radiation
Indication: Brain Neoplasm
Other drugs received by patient: Atorvastatin; Lopressor; Keppra
Possible Temodar side effects in
Reported by a physician from United States on 2012-08-10
Patient:
Reactions: Mental Status Changes, Nephrogenic Diabetes Insipidus
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Temodar
Other drugs received by patient: Atorvastatin; Keppra; Lopressor
Possible Temodar side effects in 57 year old male
Reported by a consumer/non-health professional from United States on 2012-04-10
Patient: 57 year old male, weighing 83.9 kg (184.6 pounds)
Reactions: Brain Stem Stroke
Adverse event resulted in: life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Temodar
Possible Temodar side effects in 56 year old female
Reported by a health professional (non-physician/pharmacist) from United States on 2011-11-18
Patient: 56 year old female
Reactions: Rash Generalised, Swelling Face, Urticaria, Eye Swelling
Adverse event resulted in: life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Temodar
Other drugs received by patient: Keppra; Decadron
Possible Temodar side effects in female
Reported by a consumer/non-health professional from United States on 2011-10-21
Patient: female
Reactions: Platelet Count Decreased
Adverse event resulted in: life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Temodar
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