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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 failure? 27 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Device failure have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.4% of all adverse event reports for RISEDRONATE.

27
Reports of Device failure with RISEDRONATE
0.4%
of all RISEDRONATE reports
3
Deaths
24
Hospitalizations

How Dangerous Is Device failure From RISEDRONATE?

Of the 27 reports, 3 (11.1%) resulted in death, 24 (88.9%) required hospitalization, and 3 (11.1%) were considered life-threatening.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 27 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 failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which RISEDRONATE Alternatives Have Lower Device failure 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 failure Reports All Drugs Causing Device failure RISEDRONATE Demographics