Does ROTIGOTINE Cause Intentional product misuse? 148 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 148 reports of Intentional product misuse have been filed in association with ROTIGOTINE (Neupro). This represents 1.9% of all adverse event reports for ROTIGOTINE.
148
Reports of Intentional product misuse with ROTIGOTINE
1.9%
of all ROTIGOTINE reports
7
Deaths
25
Hospitalizations
How Dangerous Is Intentional product misuse From ROTIGOTINE?
Of the 148 reports, 7 (4.7%) resulted in death, 25 (16.9%) required hospitalization, and 2 (1.4%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 148 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ROTIGOTINE Alternatives Have Lower Intentional product misuse Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI