Does SIRUKUMAB Cause Incorrect product administration duration? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Incorrect product administration duration have been filed in association with SIRUKUMAB. This represents 3.9% of all adverse event reports for SIRUKUMAB.
53
Reports of Incorrect product administration duration with SIRUKUMAB
3.9%
of all SIRUKUMAB reports
53
Deaths
52
Hospitalizations
How Dangerous Is Incorrect product administration duration From SIRUKUMAB?
Of the 53 reports, 53 (100.0%) resulted in death, 52 (98.1%) required hospitalization, and 52 (98.1%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIRUKUMAB. However, 53 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which SIRUKUMAB Alternatives Have Lower Incorrect product administration duration Risk?
SIRUKUMAB vs SITAGLIPTIN
SIRUKUMAB vs SOAP
SIRUKUMAB vs SODIUM
SIRUKUMAB vs SODIUM BICARBONATE
SIRUKUMAB vs SODIUM BICARBONATE\SODIUM