Does ROTIGOTINE Cause Application site pruritus? 334 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 334 reports of Application site pruritus have been filed in association with ROTIGOTINE (Neupro). This represents 4.3% of all adverse event reports for ROTIGOTINE.
334
Reports of Application site pruritus with ROTIGOTINE
4.3%
of all ROTIGOTINE reports
8
Deaths
36
Hospitalizations
How Dangerous Is Application site pruritus From ROTIGOTINE?
Of the 334 reports, 8 (2.4%) resulted in death, 36 (10.8%) required hospitalization, and 3 (0.9%) were considered life-threatening.
Is Application site pruritus Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 334 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 erythema (330)
Hallucination (258)
What Other Drugs Cause Application site pruritus?
MINOXIDIL (3,727)
NICOTINE (2,074)
BUPRENORPHINE (1,687)
ESTRADIOL (1,181)
SUMATRIPTAN (675)
FENTANYL (501)
ESTRADIOL\NORETHINDRONE (463)
CLONIDINE (335)
INGENOL MEBUTATE (291)
OXYBUTYNIN (289)
Which ROTIGOTINE Alternatives Have Lower Application site pruritus Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI