Does ROTIGOTINE Cause Device dislocation? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device dislocation have been filed in association with ROTIGOTINE (Neupro). This represents 0.1% of all adverse event reports for ROTIGOTINE.
8
Reports of Device dislocation with ROTIGOTINE
0.1%
of all ROTIGOTINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device dislocation From ROTIGOTINE?
Of the 8 reports, 2 (25.0%) required hospitalization.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 8 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)
Application site erythema (330)
What Other Drugs Cause Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which ROTIGOTINE Alternatives Have Lower Device dislocation Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI