Does ROTIGOTINE Cause Oedema peripheral? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Oedema peripheral have been filed in association with ROTIGOTINE (Neupro). This represents 0.4% of all adverse event reports for ROTIGOTINE.
34
Reports of Oedema peripheral with ROTIGOTINE
0.4%
of all ROTIGOTINE reports
1
Deaths
12
Hospitalizations
How Dangerous Is Oedema peripheral From ROTIGOTINE?
Of the 34 reports, 1 (2.9%) resulted in death, 12 (35.3%) required hospitalization, and 1 (2.9%) were considered life-threatening.
Is Oedema peripheral Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 34 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 Oedema peripheral?
AMBRISENTAN (2,959)
TREPROSTINIL (2,816)
ADALIMUMAB (2,356)
LENALIDOMIDE (2,298)
AMLODIPINE (2,076)
PREDNISONE (2,029)
METHOTREXATE (1,939)
MACITENTAN (1,932)
RITUXIMAB (1,698)
TOCILIZUMAB (1,574)
Which ROTIGOTINE Alternatives Have Lower Oedema peripheral Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI