Does SIRUKUMAB Cause Dyspnoea? 273 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 273 reports of Dyspnoea have been filed in association with SIRUKUMAB. This represents 20.3% of all adverse event reports for SIRUKUMAB.
273
Reports of Dyspnoea with SIRUKUMAB
20.3%
of all SIRUKUMAB reports
237
Deaths
269
Hospitalizations
How Dangerous Is Dyspnoea From SIRUKUMAB?
Of the 273 reports, 237 (86.8%) resulted in death, 269 (98.5%) required hospitalization, and 236 (86.4%) 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 SIRUKUMAB. However, 273 reports have been filed with the FAERS database.
What Other Side Effects Does SIRUKUMAB Cause?
Off label use (798)
Drug ineffective (775)
Rheumatoid arthritis (663)
Nausea (656)
Pain (629)
Synovitis (623)
General physical health deterioration (619)
Rash (565)
Pericarditis (562)
Pemphigus (561)
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 SIRUKUMAB Alternatives Have Lower Dyspnoea Risk?
SIRUKUMAB vs SITAGLIPTIN
SIRUKUMAB vs SOAP
SIRUKUMAB vs SODIUM
SIRUKUMAB vs SODIUM BICARBONATE
SIRUKUMAB vs SODIUM BICARBONATE\SODIUM