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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 Maternal exposure timing unspecified? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Maternal exposure timing unspecified have been filed in association with SIRUKUMAB. This represents 1.0% of all adverse event reports for SIRUKUMAB.

14
Reports of Maternal exposure timing unspecified with SIRUKUMAB
1.0%
of all SIRUKUMAB reports
13
Deaths
14
Hospitalizations

How Dangerous Is Maternal exposure timing unspecified From SIRUKUMAB?

Of the 14 reports, 13 (92.9%) resulted in death, 14 (100.0%) required hospitalization, and 14 (100.0%) were considered life-threatening.

Is Maternal exposure timing unspecified Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIRUKUMAB. However, 14 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 Maternal exposure timing unspecified?

RITUXIMAB (402) METHOTREXATE (350) ADALIMUMAB (343) DICLOFENAC (331) TOCILIZUMAB (327) HYDROXYCHLOROQUINE (309) FOLIC ACID (304) INFLIXIMAB (303) LEFLUNOMIDE (302) SECUKINUMAB (301)

Which SIRUKUMAB Alternatives Have Lower Maternal exposure timing unspecified 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 Maternal exposure timing unspecified Reports All Drugs Causing Maternal exposure timing unspecified SIRUKUMAB Demographics