Does RISEDRONATE Cause Intentional product use issue? 192 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 192 reports of Intentional product use issue have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 2.8% of all adverse event reports for RISEDRONATE.
192
Reports of Intentional product use issue with RISEDRONATE
2.8%
of all RISEDRONATE reports
11
Deaths
137
Hospitalizations
How Dangerous Is Intentional product use issue From RISEDRONATE?
Of the 192 reports, 11 (5.7%) resulted in death, 137 (71.4%) required hospitalization, and 20 (10.4%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 192 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which RISEDRONATE Alternatives Have Lower Intentional product use issue Risk?
RISEDRONATE vs RISEDRONIC ACID
RISEDRONATE vs RISPERDAL
RISEDRONATE vs RISPERDAL CONSTA
RISEDRONATE vs RISPERIDONE
RISEDRONATE vs RITALIN