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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ROTIGOTINE Cause Complication associated with device? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Complication associated with device have been filed in association with ROTIGOTINE (Neupro). This represents 0.1% of all adverse event reports for ROTIGOTINE.

11
Reports of Complication associated with device with ROTIGOTINE
0.1%
of all ROTIGOTINE reports
11
Deaths
11
Hospitalizations

How Dangerous Is Complication associated with device From ROTIGOTINE?

Of the 11 reports, 11 (100.0%) resulted in death, 11 (100.0%) required hospitalization, and 1 (9.1%) were considered life-threatening.

Is Complication associated with device 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 Complication associated with device?

ETONOGESTREL (6,047) COPPER (1,083) BACLOFEN (525) TREPROSTINIL (422) EPOPROSTENOL (399) LEVONORGESTREL (344) ADALIMUMAB (269) CARBIDOPA\LEVODOPA (169) MACITENTAN (169) TEDUGLUTIDE (133)

Which ROTIGOTINE Alternatives Have Lower Complication associated with device Risk?

ROTIGOTINE vs ROXADUSTAT ROTIGOTINE vs ROXICODONE ROTIGOTINE vs ROXITHROMYCIN ROTIGOTINE vs ROZANOLIXIZUMAB ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI

Related Pages

ROTIGOTINE Full Profile All Complication associated with device Reports All Drugs Causing Complication associated with device ROTIGOTINE Demographics