Does ROTIGOTINE Cause Device adhesion issue? 383 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 383 reports of Device adhesion issue have been filed in association with ROTIGOTINE (Neupro). This represents 4.9% of all adverse event reports for ROTIGOTINE.
383
Reports of Device adhesion issue with ROTIGOTINE
4.9%
of all ROTIGOTINE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device adhesion issue From ROTIGOTINE?
Of the 383 reports, 5 (1.3%) required hospitalization.
Is Device adhesion issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 383 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)
Overdose (353)
Application site pruritus (334)
Application site erythema (330)
Hallucination (258)
What Other Drugs Cause Device adhesion issue?
PEGFILGRASTIM (11,326)
ESTRADIOL (678)
METHYLPHENIDATE (302)
ESTRADIOL\LEVONORGESTREL (195)
FENTANYL\FENTANYL (190)
FENTANYL (149)
TREPROSTINIL (128)
BUPRENORPHINE (42)
ESTRADIOL\NORETHINDRONE (37)
SUMATRIPTAN (28)
Which ROTIGOTINE Alternatives Have Lower Device adhesion issue Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI