Does SECUKINUMAB Cause Product dispensing error? 300 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 300 reports of Product dispensing error have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.2% of all adverse event reports for SECUKINUMAB.
300
Reports of Product dispensing error with SECUKINUMAB
0.2%
of all SECUKINUMAB reports
2
Deaths
11
Hospitalizations
How Dangerous Is Product dispensing error From SECUKINUMAB?
Of the 300 reports, 2 (0.7%) resulted in death, 11 (3.7%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 300 reports have been filed with the FAERS database.
What Other Side Effects Does SECUKINUMAB Cause?
Drug ineffective (27,434)
Psoriasis (21,976)
Pain (15,244)
Arthralgia (13,769)
Fatigue (9,406)
Psoriatic arthropathy (8,900)
Pruritus (8,755)
Malaise (8,570)
Rash (8,023)
Condition aggravated (7,536)
What Other Drugs Cause Product dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
APIXABAN (299)
PALBOCICLIB (299)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (296)
Which SECUKINUMAB Alternatives Have Lower Product dispensing error Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG