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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 RISEDRONATE Cause Device breakage? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Device breakage have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.2% of all adverse event reports for RISEDRONATE.

12
Reports of Device breakage with RISEDRONATE
0.2%
of all RISEDRONATE reports
0
Deaths
8
Hospitalizations

How Dangerous Is Device breakage From RISEDRONATE?

Of the 12 reports, 8 (66.7%) required hospitalization.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does RISEDRONATE Cause?

Drug hypersensitivity (1,124) Asthma (1,087) Pain (973) Vomiting (971) Drug ineffective (919) Dyspnoea (898) Pneumonia (807) Wheezing (772) Oedema (708) Malaise (668)

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 RISEDRONATE Alternatives Have Lower Device breakage Risk?

RISEDRONATE vs RISEDRONIC ACID RISEDRONATE vs RISPERDAL RISEDRONATE vs RISPERDAL CONSTA RISEDRONATE vs RISPERIDONE RISEDRONATE vs RITALIN

Related Pages

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