Index of reports
> Disability (1)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Didronel (Etidronate) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Didronel side effects in female
Reported by a physician from Finland on 2012-07-13
Patient: female
Reactions: Femur Fracture, Fracture Delayed Union, Hand Fracture
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Didronel
Administration route: Oral
Indication: Osteoporosis
Fosamax
Administration route: Oral
Indication: Osteoporosis
Boniva
Administration route: Oral
Indication: Osteoporosis
Start date: 2007-01-01
End date: 2010-01-01
Calcium
Administration route: Oral
Indication: Osteoporosis
Zoledronoc Acid
Indication: Osteoporosis
Other drugs received by patient: Medrol; Vitamin D; Calcium; Humira
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