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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 Physical deconditioning? 182 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 182 reports of Physical deconditioning have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.1% of all adverse event reports for TOFACITINIB.

182
Reports of Physical deconditioning with TOFACITINIB
0.1%
of all TOFACITINIB reports
2
Deaths
13
Hospitalizations

How Dangerous Is Physical deconditioning From TOFACITINIB?

Of the 182 reports, 2 (1.1%) resulted in death, 13 (7.1%) required hospitalization, and 40 (22.0%) were considered life-threatening.

Is Physical deconditioning Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 182 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 Physical deconditioning?

ACETAMINOPHEN (193) ESOMEPRAZOLE (189) AMLODIPINE (186) FLUOXETINE (184) ESCITALOPRAM OXALATE (181) MOCLOBEMIDE (178) VALSARTAN (176) VENLAFAXINE (176) TRAMADOL (173) PEMBROLIZUMAB (72)

Which TOFACITINIB Alternatives Have Lower Physical deconditioning Risk?

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

Related Pages

TOFACITINIB Full Profile All Physical deconditioning Reports All Drugs Causing Physical deconditioning TOFACITINIB Demographics