Does FOSAMAX PLUS D Cause Device breakage? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device breakage have been filed in association with FOSAMAX PLUS D. This represents 3.6% of all adverse event reports for FOSAMAX PLUS D.
5
Reports of Device breakage with FOSAMAX PLUS D
3.6%
of all FOSAMAX PLUS D reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device breakage From FOSAMAX PLUS D?
Of the 5 reports, 5 (100.0%) 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 PLUS D. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does FOSAMAX PLUS D Cause?
Femur fracture (124)
Intramedullary rod insertion (90)
Osteoarthritis (80)
Fall (74)
Hypertension (58)
Low turnover osteopathy (45)
Osteoporosis (44)
Gastrooesophageal reflux disease (43)
Depression (38)
Arthralgia (37)
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 PLUS D Alternatives Have Lower Device breakage Risk?
FOSAMAX PLUS D vs FOSAPREPITANT
FOSAMAX PLUS D vs FOSAPREPITANT DIMEGLUMINE
FOSAMAX PLUS D vs FOSCARNET
FOSAMAX PLUS D vs FOSFOMYCIN
FOSAMAX PLUS D vs FOSFOMYCIN TROMETHAMINE