Does ROTIGOTINE Cause Application site erythema? 330 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 330 reports of Application site erythema have been filed in association with ROTIGOTINE (Neupro). This represents 4.2% of all adverse event reports for ROTIGOTINE.
330
Reports of Application site erythema with ROTIGOTINE
4.2%
of all ROTIGOTINE reports
6
Deaths
38
Hospitalizations
How Dangerous Is Application site erythema From ROTIGOTINE?
Of the 330 reports, 6 (1.8%) resulted in death, 38 (11.5%) required hospitalization, and 1 (0.3%) 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 ROTIGOTINE. However, 330 reports have been filed with the FAERS database.
What Other Side Effects Does ROTIGOTINE Cause?
Product adhesion issue (1,718)
Off label use (646)
Drug ineffective (632)
Death (595)
Parkinson's disease (419)
Fall (412)
Device adhesion issue (383)
Overdose (353)
Application site pruritus (334)
Hallucination (258)
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 ROTIGOTINE Alternatives Have Lower Application site erythema Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI