Does ROTIGOTINE Cause Application site reaction? 110 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Application site reaction have been filed in association with ROTIGOTINE (Neupro). This represents 1.4% of all adverse event reports for ROTIGOTINE.
110
Reports of Application site reaction with ROTIGOTINE
1.4%
of all ROTIGOTINE reports
1
Deaths
8
Hospitalizations
How Dangerous Is Application site reaction From ROTIGOTINE?
Of the 110 reports, 1 (0.9%) resulted in death, 8 (7.3%) required hospitalization.
Is Application site reaction Listed in the Official Label?
Yes, Application site reaction is listed as a known adverse reaction in the official FDA drug label for ROTIGOTINE.
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 Application site reaction?
NICOTINE (640)
BUPRENORPHINE (503)
FENTANYL (223)
CHLORHEXIDINE\ISOPROPYL ALCOHOL (216)
MINOXIDIL (179)
INGENOL MEBUTATE (160)
ESTRADIOL (157)
SUMATRIPTAN (86)
DICLOFENAC (72)
ESTRADIOL\NORETHINDRONE (59)
Which ROTIGOTINE Alternatives Have Lower Application site reaction Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI