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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 GUSELKUMAB Cause Hyperhidrosis? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Hyperhidrosis have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.1% of all adverse event reports for GUSELKUMAB.

24
Reports of Hyperhidrosis with GUSELKUMAB
0.1%
of all GUSELKUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Hyperhidrosis From GUSELKUMAB?

Of the 24 reports, 1 (4.2%) required hospitalization.

Is Hyperhidrosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 24 reports have been filed with the FAERS database.

What Other Side Effects Does GUSELKUMAB Cause?

Product dose omission issue (9,267) Accidental exposure to product (2,941) Drug ineffective (1,971) Needle issue (1,933) Psoriasis (1,817) Device issue (1,613) Device malfunction (1,410) Off label use (1,186) Product storage error (1,017) Inappropriate schedule of product administration (830)

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)