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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FOSAMAX Cause Device breakage? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Device breakage have been filed in association with FOSAMAX. This represents 3.2% of all adverse event reports for FOSAMAX.

31
Reports of Device breakage with FOSAMAX
3.2%
of all FOSAMAX reports
3
Deaths
29
Hospitalizations

How Dangerous Is Device breakage From FOSAMAX?

Of the 31 reports, 3 (9.7%) resulted in death, 29 (93.5%) required hospitalization.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FOSAMAX. However, 31 reports have been filed with the FAERS database.

What Other Side Effects Does FOSAMAX Cause?

Femur fracture (676) Intramedullary rod insertion (372) Osteoarthritis (322) Fall (298) Low turnover osteopathy (259) Hypertension (249) Arthralgia (198) Gastrooesophageal reflux disease (196) Depression (170) Osteoporosis (168)

What Other Drugs Cause Device breakage?

COPPER (9,201) SOMATROPIN (7,761) ETONOGESTREL (4,140) LEVONORGESTREL (2,726) ETHINYL ESTRADIOL\ETONOGESTREL (741) CARBIDOPA\LEVODOPA (634) TREPROSTINIL (396) ADALIMUMAB (375) ALBUTEROL (256) EPOPROSTENOL (240)

Which FOSAMAX Alternatives Have Lower Device breakage Risk?

FOSAMAX vs FOSAMAX PLUS D FOSAMAX vs FOSAMPRENAVIR FOSAMAX vs FOSAPREPITANT FOSAMAX vs FOSAPREPITANT DIMEGLUMINE FOSAMAX vs FOSCARBIDOPA\FOSLEVODOPA

Related Pages

FOSAMAX Full Profile All Device breakage Reports All Drugs Causing Device breakage FOSAMAX Demographics