Does ROTIGOTINE Cause Therapy interrupted? 186 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 186 reports of Therapy interrupted have been filed in association with ROTIGOTINE (Neupro). This represents 2.4% of all adverse event reports for ROTIGOTINE.
186
Reports of Therapy interrupted with ROTIGOTINE
2.4%
of all ROTIGOTINE reports
4
Deaths
44
Hospitalizations
How Dangerous Is Therapy interrupted From ROTIGOTINE?
Of the 186 reports, 4 (2.2%) resulted in death, 44 (23.7%) required hospitalization, and 2 (1.1%) were considered life-threatening.
Is Therapy interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 186 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 Therapy interrupted?
ADALIMUMAB (5,755)
ETANERCEPT (3,397)
RELUGOLIX (3,251)
CERTOLIZUMAB PEGOL (3,209)
LENALIDOMIDE (2,724)
UPADACITINIB (1,741)
ABATACEPT (1,726)
CLOZAPINE (1,722)
AMIKACIN (1,283)
TOFACITINIB (1,182)
Which ROTIGOTINE Alternatives Have Lower Therapy interrupted Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI