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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SECUKINUMAB Cause Condition aggravated? 7,536 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7,536 reports of Condition aggravated have been filed in association with SECUKINUMAB (COSENTYX). This represents 5.0% of all adverse event reports for SECUKINUMAB.

7,536
Reports of Condition aggravated with SECUKINUMAB
5.0%
of all SECUKINUMAB reports
1,526
Deaths
2,225
Hospitalizations

How Dangerous Is Condition aggravated From SECUKINUMAB?

Of the 7,536 reports, 1,526 (20.2%) resulted in death, 2,225 (29.5%) required hospitalization, and 1,786 (23.7%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 7,536 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) Diarrhoea (7,131)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which SECUKINUMAB Alternatives Have Lower Condition aggravated Risk?

SECUKINUMAB vs SELADELPAR LYSINE SECUKINUMAB vs SELEGILINE SECUKINUMAB vs SELENIUM SECUKINUMAB vs SELENIUM SULFIDE SECUKINUMAB vs SELEXIPAG

Related Pages

SECUKINUMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated SECUKINUMAB Demographics