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Didronel (Etidronate) - Disability - Suspected Cause - Side Effect Reports

 
 



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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