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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 Unresponsive to stimuli? 11 Reports in FDA Database

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

11
Reports of Unresponsive to stimuli with ROTIGOTINE
0.1%
of all ROTIGOTINE reports
1
Deaths
5
Hospitalizations

How Dangerous Is Unresponsive to stimuli From ROTIGOTINE?

Of the 11 reports, 1 (9.1%) resulted in death, 5 (45.5%) required hospitalization.

Is Unresponsive to stimuli 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 Unresponsive to stimuli?

OXYCODONE (738) FENTANYL (662) QUETIAPINE (542) MORPHINE (483) BACLOFEN (464) CARBIDOPA\LEVODOPA (417) ACETAMINOPHEN (406) CLONAZEPAM (385) METFORMIN (360) OLANZAPINE (353)

Which ROTIGOTINE Alternatives Have Lower Unresponsive to stimuli Risk?

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

Related Pages

ROTIGOTINE Full Profile All Unresponsive to stimuli Reports All Drugs Causing Unresponsive to stimuli ROTIGOTINE Demographics