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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 Dehydration? 399 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 399 reports of Dehydration have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.3% of all adverse event reports for TOFACITINIB.

399
Reports of Dehydration with TOFACITINIB
0.3%
of all TOFACITINIB reports
13
Deaths
224
Hospitalizations

How Dangerous Is Dehydration From TOFACITINIB?

Of the 399 reports, 13 (3.3%) resulted in death, 224 (56.1%) required hospitalization, and 6 (1.5%) were considered life-threatening.

Is Dehydration Listed in the Official Label?

Yes, Dehydration is listed as a known adverse reaction in the official FDA drug label for TOFACITINIB.

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 Dehydration?

LENALIDOMIDE (3,469) ADALIMUMAB (3,233) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (3,168) FUROSEMIDE (2,195) SEMAGLUTIDE (1,816) METFORMIN (1,754) CAPECITABINE (1,599) LENVATINIB (1,526) TIRZEPATIDE (1,187) SACUBITRIL\VALSARTAN (1,171)

Which TOFACITINIB Alternatives Have Lower Dehydration Risk?

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

Related Pages

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