Does SELEGILINE Cause Condition aggravated? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Condition aggravated have been filed in association with SELEGILINE (ZELAPAR). This represents 1.9% of all adverse event reports for SELEGILINE.
18
Reports of Condition aggravated with SELEGILINE
1.9%
of all SELEGILINE reports
2
Deaths
0
Hospitalizations
How Dangerous Is Condition aggravated From SELEGILINE?
Of the 18 reports, 2 (11.1%) resulted in death.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SELEGILINE. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does SELEGILINE Cause?
Drug ineffective (134)
Application site erythema (92)
Insomnia (71)
Application site pruritus (65)
Hallucination (54)
Drug interaction (53)
Application site rash (51)
Dizziness (46)
Dyskinesia (45)
Off label use (45)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which SELEGILINE Alternatives Have Lower Condition aggravated Risk?
SELEGILINE vs SELENIUM
SELEGILINE vs SELENIUM SULFIDE
SELEGILINE vs SELEXIPAG
SELEGILINE vs SELINEXOR
SELEGILINE vs SELPERCATINIB