Does SECUKINUMAB Cause Device malfunction? 2,259 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,259 reports of Device malfunction have been filed in association with SECUKINUMAB (COSENTYX). This represents 1.5% of all adverse event reports for SECUKINUMAB.
2,259
Reports of Device malfunction with SECUKINUMAB
1.5%
of all SECUKINUMAB reports
2
Deaths
63
Hospitalizations
How Dangerous Is Device malfunction From SECUKINUMAB?
Of the 2,259 reports, 2 (0.1%) resulted in death, 63 (2.8%) required hospitalization, and 16 (0.7%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 2,259 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which SECUKINUMAB Alternatives Have Lower Device malfunction Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG