Does CERTOLIZUMAB PEGOL Cause Maternal exposure timing unspecified? 285 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 285 reports of Maternal exposure timing unspecified have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.3% of all adverse event reports for CERTOLIZUMAB PEGOL.
285
Reports of Maternal exposure timing unspecified with CERTOLIZUMAB PEGOL
0.3%
of all CERTOLIZUMAB PEGOL reports
178
Deaths
203
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From CERTOLIZUMAB PEGOL?
Of the 285 reports, 178 (62.5%) resulted in death, 203 (71.2%) required hospitalization, and 192 (67.4%) 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 CERTOLIZUMAB PEGOL. However, 285 reports have been filed with the FAERS database.
What Other Side Effects Does CERTOLIZUMAB PEGOL Cause?
Drug ineffective (23,838)
Rheumatoid arthritis (17,782)
Pain (13,929)
Fatigue (11,438)
Off label use (10,281)
Rash (9,663)
Alopecia (9,111)
Maternal exposure during pregnancy (9,013)
Arthralgia (8,993)
Abdominal discomfort (8,615)
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 CERTOLIZUMAB PEGOL Alternatives Have Lower Maternal exposure timing unspecified Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX