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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 Dyspnoea? 4,100 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 4,100 reports of Dyspnoea have been filed in association with SECUKINUMAB (COSENTYX). This represents 2.7% of all adverse event reports for SECUKINUMAB.

4,100
Reports of Dyspnoea with SECUKINUMAB
2.7%
of all SECUKINUMAB reports
1,185
Deaths
2,153
Hospitalizations

How Dangerous Is Dyspnoea From SECUKINUMAB?

Of the 4,100 reports, 1,185 (28.9%) resulted in death, 2,153 (52.5%) required hospitalization, and 1,409 (34.4%) were considered life-threatening.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 4,100 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 Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

Which SECUKINUMAB Alternatives Have Lower Dyspnoea Risk?

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

Related Pages

SECUKINUMAB Full Profile All Dyspnoea Reports All Drugs Causing Dyspnoea SECUKINUMAB Demographics