Does RISEDRONATE Cause Wrong patient received product? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong patient received product have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.1% of all adverse event reports for RISEDRONATE.
5
Reports of Wrong patient received product with RISEDRONATE
0.1%
of all RISEDRONATE reports
3
Deaths
0
Hospitalizations
How Dangerous Is Wrong patient received product From RISEDRONATE?
Of the 5 reports, 3 (60.0%) resulted in death.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 5 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 Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which RISEDRONATE Alternatives Have Lower Wrong patient received product Risk?
RISEDRONATE vs RISEDRONIC ACID
RISEDRONATE vs RISPERDAL
RISEDRONATE vs RISPERDAL CONSTA
RISEDRONATE vs RISPERIDONE
RISEDRONATE vs RITALIN