Does SELEGILINE Cause Wrong technique in product usage process? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Wrong technique in product usage process have been filed in association with SELEGILINE (ZELAPAR). This represents 3.5% of all adverse event reports for SELEGILINE.
33
Reports of Wrong technique in product usage process with SELEGILINE
3.5%
of all SELEGILINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SELEGILINE?
Of the 33 reports.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SELEGILINE. However, 33 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which SELEGILINE Alternatives Have Lower Wrong technique in product usage process Risk?
SELEGILINE vs SELENIUM
SELEGILINE vs SELENIUM SULFIDE
SELEGILINE vs SELEXIPAG
SELEGILINE vs SELINEXOR
SELEGILINE vs SELPERCATINIB