Does RIVASTIGMINE Cause Incorrect product administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product administration duration have been filed in association with RIVASTIGMINE (Exelon). This represents 0.1% of all adverse event reports for RIVASTIGMINE.
8
Reports of Incorrect product administration duration with RIVASTIGMINE
0.1%
of all RIVASTIGMINE reports
1
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product administration duration From RIVASTIGMINE?
Of the 8 reports, 1 (12.5%) resulted in death, 4 (50.0%) required hospitalization, and 2 (25.0%) 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 RIVASTIGMINE. However, 8 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 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 RIVASTIGMINE Alternatives Have Lower Incorrect product administration duration Risk?
RIVASTIGMINE vs RIVOTRIL
RIVASTIGMINE vs RIZATRIPTAN
RIVASTIGMINE vs ROACTEMRA
RIVASTIGMINE vs ROCURONIUM
RIVASTIGMINE vs ROFECOXIB