Does RISEDRONATE Cause Product administration error? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product administration error have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.1% of all adverse event reports for RISEDRONATE.
9
Reports of Product administration error with RISEDRONATE
0.1%
of all RISEDRONATE reports
2
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From RISEDRONATE?
Of the 9 reports, 2 (22.2%) resulted in death.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 9 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which RISEDRONATE Alternatives Have Lower Product administration error Risk?
RISEDRONATE vs RISEDRONIC ACID
RISEDRONATE vs RISPERDAL
RISEDRONATE vs RISPERDAL CONSTA
RISEDRONATE vs RISPERIDONE
RISEDRONATE vs RITALIN