Does ROTIGOTINE Cause Ill-defined disorder? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Ill-defined disorder have been filed in association with ROTIGOTINE (Neupro). This represents 0.1% of all adverse event reports for ROTIGOTINE.
11
Reports of Ill-defined disorder with ROTIGOTINE
0.1%
of all ROTIGOTINE reports
3
Deaths
6
Hospitalizations
How Dangerous Is Ill-defined disorder From ROTIGOTINE?
Of the 11 reports, 3 (27.3%) resulted in death, 6 (54.5%) required hospitalization.
Is Ill-defined disorder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 11 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 Ill-defined disorder?
ACETAMINOPHEN\OXYCODONE (9,780)
ACETAMINOPHEN\HYDROCODONE (6,159)
TOCILIZUMAB (4,411)
RITUXIMAB (4,220)
ETANERCEPT (4,202)
METHOTREXATE (4,063)
ABATACEPT (3,630)
LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600)
LEFLUNOMIDE (3,570)
CERTOLIZUMAB PEGOL (3,273)
Which ROTIGOTINE Alternatives Have Lower Ill-defined disorder Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI