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Index of reports
> Disability (1)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Dantrium (Dantrolene) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Dantrium side effects in 59 year old female
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-08-17
Patient: 59 year old female, weighing 40.0 kg (88.0 pounds)
Reactions: Jaundice, Liver Disorder
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Dantrium
Administration route: Oral
End date: 2011-08-12
Pramipexole Dihydrochloride
Administration route: Oral
End date: 2011-08-05
Other drugs received by patient: Plavix; Atelec; Candesartan Cilexetil and Hydrochlorothiazide
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