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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 Tiazac (Diltiazem) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Tiazac side effects in 85 year old female
Reported by a individual with unspecified qualification from United States on 2012-02-09
Patient: 85 year old female
Reactions: Cardiac Valve Disease, Heart Rate Decreased, Cardiac Failure Congestive, Cardiac Disorder
Adverse event resulted in: life threatening event, disablity
Drug(s) suspected as cause:
Tiazac
Dosage: 160 mg 1 per day oral
Administration route: Oral
Indication: Blood Potassium Increased
Start date: 2003-03-06
End date: 2003-03-17
Tiazac
Dosage: 160 mg 1 per day oral
Administration route: Oral
Indication: Heart Rate Irregular
Start date: 2003-03-06
End date: 2003-03-17
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