Does ABATACEPT Cause Maternal exposure timing unspecified? 275 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 275 reports of Maternal exposure timing unspecified have been filed in association with ABATACEPT (ORENCIA). This represents 0.2% of all adverse event reports for ABATACEPT.
275
Reports of Maternal exposure timing unspecified with ABATACEPT
0.2%
of all ABATACEPT reports
172
Deaths
196
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ABATACEPT?
Of the 275 reports, 172 (62.5%) resulted in death, 196 (71.3%) required hospitalization, and 187 (68.0%) 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 ABATACEPT. However, 275 reports have been filed with the FAERS database.
What Other Side Effects Does ABATACEPT Cause?
Drug ineffective (35,212)
Rheumatoid arthritis (21,898)
Pain (19,783)
Arthralgia (18,536)
Joint swelling (18,453)
Contraindicated product administered (13,559)
Fatigue (13,087)
Drug intolerance (12,451)
Rash (12,168)
Arthropathy (11,099)
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 ABATACEPT Alternatives Have Lower Maternal exposure timing unspecified Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE