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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 TOFACITINIB Cause Abasia? 76 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Abasia have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.1% of all adverse event reports for TOFACITINIB.

76
Reports of Abasia with TOFACITINIB
0.1%
of all TOFACITINIB reports
1
Deaths
14
Hospitalizations

How Dangerous Is Abasia From TOFACITINIB?

Of the 76 reports, 1 (1.3%) resulted in death, 14 (18.4%) required hospitalization.

Is Abasia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 76 reports have been filed with the FAERS database.

What Other Side Effects Does TOFACITINIB Cause?

Drug ineffective (30,382) Pain (21,659) Condition aggravated (16,925) Arthralgia (15,640) Fatigue (13,551) Rheumatoid arthritis (12,277) Off label use (11,736) Headache (11,061) Joint swelling (10,686) Malaise (9,040)

What Other Drugs Cause Abasia?

ETANERCEPT (735) ADALIMUMAB (580) INTERFERON BETA-1A (502) DALFAMPRIDINE (480) DIMETHYL (444) NATALIZUMAB (362) PREGABALIN (355) LEVOFLOXACIN (178) DENOSUMAB (165) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (160)

Which TOFACITINIB Alternatives Have Lower Abasia Risk?

TOFACITINIB vs TOFERSEN TOFACITINIB vs TOLNAFTATE TOFACITINIB vs TOLODODEKIN ALFA TOFACITINIB vs TOLTERODINE TOFACITINIB vs TOLVAPTAN

Related Pages

TOFACITINIB Full Profile All Abasia Reports All Drugs Causing Abasia TOFACITINIB Demographics