Index of reports
> Disability (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Detrol (Tolterodine) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Detrol side effects in female
Reported by a consumer/non-health professional from United States on 2012-07-03
Patient: female
Reactions: Road Traffic Accident
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Chantix
Dosage: unk
Start date: 2009-05-22
Detrol
Dosage: unk
Start date: 2009-05-22
Lipitor
Dosage: unk
Start date: 2009-05-22
Possible Detrol side effects in female
Reported by a consumer/non-health professional from United States on 2012-03-22
Patient: female, weighing 54.4 kg (119.7 pounds)
Reactions: Drug Ineffective, Pain, Grip Strength Decreased, Rotator Cuff Syndrome
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Acetaminophen and Hydrocodone Bitartrate
Dosage: 5/500 mg, 2x/day
Administration route: Oral
Indication: Pain
Detrol
Dosage: 10 mg, 2x/day
Indication: Urinary Incontinence
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