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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 CERTOLIZUMAB Cause Condition aggravated? 36 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Condition aggravated have been filed in association with CERTOLIZUMAB. This represents 6.8% of all adverse event reports for CERTOLIZUMAB.

36
Reports of Condition aggravated with CERTOLIZUMAB
6.8%
of all CERTOLIZUMAB reports
2
Deaths
11
Hospitalizations

How Dangerous Is Condition aggravated From CERTOLIZUMAB?

Of the 36 reports, 2 (5.6%) resulted in death, 11 (30.6%) required hospitalization, and 3 (8.3%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB. However, 36 reports have been filed with the FAERS database.

What Other Side Effects Does CERTOLIZUMAB Cause?

Drug ineffective (156) Infection (71) Off label use (64) Rheumatoid arthritis (53) Drug intolerance (51) Arthritis (44) Therapeutic product effect decreased (39) Treatment failure (36) Pneumonia (35) Psoriasis (35)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which CERTOLIZUMAB Alternatives Have Lower Condition aggravated Risk?

CERTOLIZUMAB vs CERTOLIZUMAB PEGOL CERTOLIZUMAB vs CERTOPARIN CERTOLIZUMAB vs CETIRIZINE CERTOLIZUMAB vs CETIRIZINE\PSEUDOEPHEDRINE CERTOLIZUMAB vs CETRIMIDE

Related Pages

CERTOLIZUMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated CERTOLIZUMAB Demographics