Does SECUKINUMAB Cause Post procedural complication? 97 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 97 reports of Post procedural complication have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.1% of all adverse event reports for SECUKINUMAB.
97
Reports of Post procedural complication with SECUKINUMAB
0.1%
of all SECUKINUMAB reports
5
Deaths
49
Hospitalizations
How Dangerous Is Post procedural complication From SECUKINUMAB?
Of the 97 reports, 5 (5.2%) resulted in death, 49 (50.5%) required hospitalization, and 2 (2.1%) were considered life-threatening.
Is Post procedural complication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 97 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 Post procedural complication?
ADALIMUMAB (2,494)
ETANERCEPT (318)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244)
UPADACITINIB (241)
RISANKIZUMAB-RZAA (232)
INFLIXIMAB (217)
METHOTREXATE (188)
TREPROSTINIL (174)
HUMAN IMMUNOGLOBULIN G (159)
PREDNISONE (157)
Which SECUKINUMAB Alternatives Have Lower Post procedural complication Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG