Does RIVASTIGMINE Cause Product prescribing error? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Product prescribing error have been filed in association with RIVASTIGMINE (Exelon). This represents 0.5% of all adverse event reports for RIVASTIGMINE.
47
Reports of Product prescribing error with RIVASTIGMINE
0.5%
of all RIVASTIGMINE reports
3
Deaths
28
Hospitalizations
How Dangerous Is Product prescribing error From RIVASTIGMINE?
Of the 47 reports, 3 (6.4%) resulted in death, 28 (59.6%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIVASTIGMINE. However, 47 reports have been filed with the FAERS database.
What Other Side Effects Does RIVASTIGMINE Cause?
Death (1,229)
Fall (587)
Malaise (514)
Drug ineffective (510)
Product adhesion issue (478)
Vomiting (432)
Dementia alzheimer's type (428)
Memory impairment (385)
Nausea (383)
Pneumonia (378)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which RIVASTIGMINE Alternatives Have Lower Product prescribing error Risk?
RIVASTIGMINE vs RIVOTRIL
RIVASTIGMINE vs RIZATRIPTAN
RIVASTIGMINE vs ROACTEMRA
RIVASTIGMINE vs ROCURONIUM
RIVASTIGMINE vs ROFECOXIB