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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 SIRUKUMAB Cause Product quality issue? 228 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 228 reports of Product quality issue have been filed in association with SIRUKUMAB. This represents 17.0% of all adverse event reports for SIRUKUMAB.

228
Reports of Product quality issue with SIRUKUMAB
17.0%
of all SIRUKUMAB reports
228
Deaths
189
Hospitalizations

How Dangerous Is Product quality issue From SIRUKUMAB?

Of the 228 reports, 228 (100.0%) resulted in death, 189 (82.9%) required hospitalization, and 189 (82.9%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIRUKUMAB. However, 228 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 Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which SIRUKUMAB Alternatives Have Lower Product quality issue Risk?

SIRUKUMAB vs SITAGLIPTIN SIRUKUMAB vs SOAP SIRUKUMAB vs SODIUM SIRUKUMAB vs SODIUM BICARBONATE SIRUKUMAB vs SODIUM BICARBONATE\SODIUM

Related Pages

SIRUKUMAB Full Profile All Product quality issue Reports All Drugs Causing Product quality issue SIRUKUMAB Demographics