Does SECUKINUMAB Cause Device defective? 666 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 666 reports of Device defective have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.4% of all adverse event reports for SECUKINUMAB.
666
Reports of Device defective with SECUKINUMAB
0.4%
of all SECUKINUMAB reports
4
Deaths
41
Hospitalizations
How Dangerous Is Device defective From SECUKINUMAB?
Of the 666 reports, 4 (0.6%) resulted in death, 41 (6.2%) required hospitalization, and 26 (3.9%) were considered life-threatening.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 666 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
BUDESONIDE\FORMOTEROL (378)
Which SECUKINUMAB Alternatives Have Lower Device defective Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG