Does SELEGILINE Cause Intentional product misuse? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Intentional product misuse have been filed in association with SELEGILINE (ZELAPAR). This represents 1.4% of all adverse event reports for SELEGILINE.
13
Reports of Intentional product misuse with SELEGILINE
1.4%
of all SELEGILINE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Intentional product misuse From SELEGILINE?
Of the 13 reports, 8 (61.5%) required hospitalization, and 2 (15.4%) 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 SELEGILINE. However, 13 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 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 SELEGILINE Alternatives Have Lower Intentional product misuse Risk?
SELEGILINE vs SELENIUM
SELEGILINE vs SELENIUM SULFIDE
SELEGILINE vs SELEXIPAG
SELEGILINE vs SELINEXOR
SELEGILINE vs SELPERCATINIB