Does RISEDRONATE Cause Complication associated with device? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Complication associated with device have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.1% of all adverse event reports for RISEDRONATE.
7
Reports of Complication associated with device with RISEDRONATE
0.1%
of all RISEDRONATE reports
0
Deaths
7
Hospitalizations
How Dangerous Is Complication associated with device From RISEDRONATE?
Of the 7 reports, 7 (100.0%) required hospitalization.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 7 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which RISEDRONATE Alternatives Have Lower Complication associated with device Risk?
RISEDRONATE vs RISEDRONIC ACID
RISEDRONATE vs RISPERDAL
RISEDRONATE vs RISPERDAL CONSTA
RISEDRONATE vs RISPERIDONE
RISEDRONATE vs RITALIN