Does SECUKINUMAB Cause Contraindicated product administered? 2,686 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,686 reports of Contraindicated product administered have been filed in association with SECUKINUMAB (COSENTYX). This represents 1.8% of all adverse event reports for SECUKINUMAB.
2,686
Reports of Contraindicated product administered with SECUKINUMAB
1.8%
of all SECUKINUMAB reports
1,142
Deaths
1,420
Hospitalizations
How Dangerous Is Contraindicated product administered From SECUKINUMAB?
Of the 2,686 reports, 1,142 (42.5%) resulted in death, 1,420 (52.9%) required hospitalization, and 1,395 (51.9%) were considered life-threatening.
Is Contraindicated product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 2,686 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 Contraindicated product administered?
ABATACEPT (13,559)
METHOTREXATE (13,121)
ETANERCEPT (12,062)
TOCILIZUMAB (11,547)
ADALIMUMAB (11,270)
LEFLUNOMIDE (11,206)
HYDROXYCHLOROQUINE (10,557)
RITUXIMAB (10,479)
INFLIXIMAB (9,618)
SULFASALAZINE (8,698)
Which SECUKINUMAB Alternatives Have Lower Contraindicated product administered Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG