Does SECUKINUMAB Cause Device leakage? 910 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 910 reports of Device leakage have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.6% of all adverse event reports for SECUKINUMAB.
910
Reports of Device leakage with SECUKINUMAB
0.6%
of all SECUKINUMAB reports
1
Deaths
23
Hospitalizations
How Dangerous Is Device leakage From SECUKINUMAB?
Of the 910 reports, 1 (0.1%) resulted in death, 23 (2.5%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 910 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
ABATACEPT (671)
Which SECUKINUMAB Alternatives Have Lower Device leakage Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG