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Kerlone (Betaxolol) - 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 Kerlone (Betaxolol) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Kerlone side effects in 68 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-10-07

Patient: 68 year old female

Reactions: Pain, Muscular Weakness

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Crestor
    Administration route: Oral
    Start date: 2006-09-01
    End date: 2009-09-01

Kerlone
    Administration route: Oral
    Start date: 2000-01-01
    End date: 2011-03-01

Kerlone
    Administration route: Oral
    Indication: Migraine
    Start date: 2000-01-01
    End date: 2011-03-01



Possible Kerlone side effects in 68 year old female

Reported by a physician from France on 2011-10-05

Patient: 68 year old female

Reactions: Pain, Muscular Weakness

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Crestor
    Administration route: Oral
    Indication: Dyslipidaemia
    Start date: 2006-09-01
    End date: 2009-09-01

Kerlone
    Administration route: Oral
    Indication: Hypertension
    Start date: 2000-01-01
    End date: 2011-03-01

Kerlone
    Administration route: Oral
    Indication: Migraine
    Start date: 2000-01-01
    End date: 2011-03-01

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