Does RIVASTIGMINE Cause Product administration error? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product administration error have been filed in association with RIVASTIGMINE (Exelon). This represents 0.3% of all adverse event reports for RIVASTIGMINE.
29
Reports of Product administration error with RIVASTIGMINE
0.3%
of all RIVASTIGMINE reports
0
Deaths
18
Hospitalizations
How Dangerous Is Product administration error From RIVASTIGMINE?
Of the 29 reports, 18 (62.1%) required hospitalization, and 2 (6.9%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIVASTIGMINE. However, 29 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 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 RIVASTIGMINE Alternatives Have Lower Product administration error Risk?
RIVASTIGMINE vs RIVOTRIL
RIVASTIGMINE vs RIZATRIPTAN
RIVASTIGMINE vs ROACTEMRA
RIVASTIGMINE vs ROCURONIUM
RIVASTIGMINE vs ROFECOXIB