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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