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Detrol (Tolterodine) - Disability - Suspected Cause - Side Effect Reports

 
 



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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