Does RISEDRONATE Cause Incorrect product administration duration? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect product administration duration have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.2% of all adverse event reports for RISEDRONATE.
14
Reports of Incorrect product administration duration with RISEDRONATE
0.2%
of all RISEDRONATE reports
2
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From RISEDRONATE?
Of the 14 reports, 2 (14.3%) resulted in death, 3 (21.4%) required hospitalization, and 2 (14.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 14 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which RISEDRONATE Alternatives Have Lower Incorrect product administration duration Risk?
RISEDRONATE vs RISEDRONIC ACID
RISEDRONATE vs RISPERDAL
RISEDRONATE vs RISPERDAL CONSTA
RISEDRONATE vs RISPERIDONE
RISEDRONATE vs RITALIN