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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 Hyperhidrosis? 636 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 636 reports of Hyperhidrosis have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.4% of all adverse event reports for TOFACITINIB.

636
Reports of Hyperhidrosis with TOFACITINIB
0.4%
of all TOFACITINIB reports
27
Deaths
99
Hospitalizations

How Dangerous Is Hyperhidrosis From TOFACITINIB?

Of the 636 reports, 27 (4.2%) resulted in death, 99 (15.6%) required hospitalization, and 17 (2.7%) were considered life-threatening.

Is Hyperhidrosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 636 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 Hyperhidrosis?

DULOXETINE (4,101) ADALIMUMAB (2,745) SODIUM (2,444) VENLAFAXINE (1,932) LEVOTHYROXINE (1,856) ACETAMINOPHEN (1,578) ETANERCEPT (1,521) MORPHINE (1,438) GABAPENTIN (1,408) PREGABALIN (1,385)

Which TOFACITINIB Alternatives Have Lower Hyperhidrosis Risk?

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

Related Pages

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