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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 ABATACEPT Cause Product use complaint? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Product use complaint have been filed in association with ABATACEPT (ORENCIA). This represents 0.0% of all adverse event reports for ABATACEPT.

21
Reports of Product use complaint with ABATACEPT
0.0%
of all ABATACEPT reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product use complaint From ABATACEPT?

Of the 21 reports, 1 (4.8%) required hospitalization.

Is Product use complaint Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 21 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 Product use complaint?

TROFINETIDE (472) ENZALUTAMIDE (336) LIFITEGRAST (326) VOXELOTOR (298) CLASCOTERONE (285) NIRMATRELVIR\RITONAVIR (248) ABALOPARATIDE (224) ESTRADIOL (208) MOLNUPIRAVIR (206) ACETAMINOPHEN (202)

Which ABATACEPT Alternatives Have Lower Product use complaint Risk?

ABATACEPT vs ABATACEPT SUBQ /ML ABATACEPT vs ABCIXIMAB ABATACEPT vs ABEMACICLIB ABATACEPT vs ABILIFY ABATACEPT vs ABIRATERONE

Related Pages

ABATACEPT Full Profile All Product use complaint Reports All Drugs Causing Product use complaint ABATACEPT Demographics