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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 Concomitant disease aggravated? 461 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 461 reports of Concomitant disease aggravated have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.3% of all adverse event reports for SECUKINUMAB.

461
Reports of Concomitant disease aggravated with SECUKINUMAB
0.3%
of all SECUKINUMAB reports
19
Deaths
109
Hospitalizations

How Dangerous Is Concomitant disease aggravated From SECUKINUMAB?

Of the 461 reports, 19 (4.1%) resulted in death, 109 (23.6%) required hospitalization, and 18 (3.9%) were considered life-threatening.

Is Concomitant disease aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 461 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 Concomitant disease aggravated?

SACUBITRIL\VALSARTAN (533) FINGOLIMOD (425) MACITENTAN (286) OMALIZUMAB (186) SELEXIPAG (166) METHOTREXATE (150) RUXOLITINIB (142) OCTREOTIDE (125) BOSENTAN (123) EVEROLIMUS (123)

Which SECUKINUMAB Alternatives Have Lower Concomitant disease 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 Concomitant disease aggravated Reports All Drugs Causing Concomitant disease aggravated SECUKINUMAB Demographics