Does SECUKINUMAB Cause Device delivery system issue? 180 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 180 reports of Device delivery system issue have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.1% of all adverse event reports for SECUKINUMAB.
180
Reports of Device delivery system issue with SECUKINUMAB
0.1%
of all SECUKINUMAB reports
0
Deaths
8
Hospitalizations
How Dangerous Is Device delivery system issue From SECUKINUMAB?
Of the 180 reports, 8 (4.4%) required hospitalization, and 3 (1.7%) were considered life-threatening.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 180 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 delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which SECUKINUMAB Alternatives Have Lower Device delivery system issue Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG