Does RIVASTIGMINE Cause Application site erythema? 301 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 301 reports of Application site erythema have been filed in association with RIVASTIGMINE (Exelon). This represents 3.3% of all adverse event reports for RIVASTIGMINE.
301
Reports of Application site erythema with RIVASTIGMINE
3.3%
of all RIVASTIGMINE reports
7
Deaths
58
Hospitalizations
How Dangerous Is Application site erythema From RIVASTIGMINE?
Of the 301 reports, 7 (2.3%) resulted in death, 58 (19.3%) required hospitalization, and 3 (1.0%) were considered life-threatening.
Is Application site erythema Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIVASTIGMINE. However, 301 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 Application site erythema?
NICOTINE (2,004)
SUMATRIPTAN (1,875)
INGENOL MEBUTATE (1,373)
BUPRENORPHINE (1,273)
ESTRADIOL (1,117)
MINOXIDIL (1,061)
METHYLPHENIDATE (543)
ESTRADIOL\NORETHINDRONE (533)
FENTANYL (501)
OXYTROL FOR WOMEN (422)
Which RIVASTIGMINE Alternatives Have Lower Application site erythema Risk?
RIVASTIGMINE vs RIVOTRIL
RIVASTIGMINE vs RIZATRIPTAN
RIVASTIGMINE vs ROACTEMRA
RIVASTIGMINE vs ROCURONIUM
RIVASTIGMINE vs ROFECOXIB