Does SECUKINUMAB Cause Device use issue? 60 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Device use issue have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.0% of all adverse event reports for SECUKINUMAB.
60
Reports of Device use issue with SECUKINUMAB
0.0%
of all SECUKINUMAB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Device use issue From SECUKINUMAB?
Of the 60 reports, 4 (6.7%) required hospitalization, and 2 (3.3%) were considered life-threatening.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 60 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 use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
Which SECUKINUMAB Alternatives Have Lower Device use issue Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG