Does SELEGILINE Cause Application site erythema? 92 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Application site erythema have been filed in association with SELEGILINE (ZELAPAR). This represents 9.9% of all adverse event reports for SELEGILINE.
92
Reports of Application site erythema with SELEGILINE
9.9%
of all SELEGILINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Application site erythema From SELEGILINE?
Of the 92 reports, 1 (1.1%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Application site erythema Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SELEGILINE. However, 92 reports have been filed with the FAERS database.
What Other Side Effects Does SELEGILINE Cause?
Drug ineffective (134)
Insomnia (71)
Application site pruritus (65)
Hallucination (54)
Drug interaction (53)
Application site rash (51)
Dizziness (46)
Dyskinesia (45)
Off label use (45)
Product adhesion issue (44)
What Other Drugs Cause Application site erythema?
NICOTINE (2,004)
SUMATRIPTAN (1,875)
INGENOL MEBUTATE (1,373)
BUPRENORPHINE (1,273)
ESTRADIOL (1,117)
MINOXIDIL (1,061)
METHYLPHENIDATE (543)
ESTRADIOL\NORETHINDRONE (533)
FENTANYL (501)
OXYTROL FOR WOMEN (422)
Which SELEGILINE Alternatives Have Lower Application site erythema Risk?
SELEGILINE vs SELENIUM
SELEGILINE vs SELENIUM SULFIDE
SELEGILINE vs SELEXIPAG
SELEGILINE vs SELINEXOR
SELEGILINE vs SELPERCATINIB