Does SECUKINUMAB Cause Adverse event? 673 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 673 reports of Adverse event have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.5% of all adverse event reports for SECUKINUMAB.
673
Reports of Adverse event with SECUKINUMAB
0.5%
of all SECUKINUMAB reports
409
Deaths
457
Hospitalizations
How Dangerous Is Adverse event From SECUKINUMAB?
Of the 673 reports, 409 (60.8%) resulted in death, 457 (67.9%) required hospitalization, and 479 (71.2%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for SECUKINUMAB.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which SECUKINUMAB Alternatives Have Lower Adverse event Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG