Does GUSELKUMAB Cause Dyspnoea? 180 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 180 reports of Dyspnoea have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.6% of all adverse event reports for GUSELKUMAB.
180
Reports of Dyspnoea with GUSELKUMAB
0.6%
of all GUSELKUMAB reports
8
Deaths
53
Hospitalizations
How Dangerous Is Dyspnoea From GUSELKUMAB?
Of the 180 reports, 8 (4.4%) resulted in death, 53 (29.4%) required hospitalization, and 7 (3.9%) 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 GUSELKUMAB. However, 180 reports have been filed with the FAERS database.
What Other Side Effects Does GUSELKUMAB Cause?
Product dose omission issue (9,267)
Accidental exposure to product (2,941)
Drug ineffective (1,971)
Needle issue (1,933)
Psoriasis (1,817)
Device issue (1,613)
Device malfunction (1,410)
Off label use (1,186)
Product storage error (1,017)
Inappropriate schedule of product administration (830)
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 GUSELKUMAB Alternatives Have Lower Dyspnoea Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE