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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 DEVICE Cause Hyperhidrosis? 98 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Hyperhidrosis have been filed in association with DEVICE. This represents 0.8% of all adverse event reports for DEVICE.

98
Reports of Hyperhidrosis with DEVICE
0.8%
of all DEVICE reports
1
Deaths
16
Hospitalizations

How Dangerous Is Hyperhidrosis From DEVICE?

Of the 98 reports, 1 (1.0%) resulted in death, 16 (16.3%) required hospitalization, and 4 (4.1%) 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 DEVICE. However, 98 reports have been filed with the FAERS database.

What Other Side Effects Does DEVICE Cause?

Blood glucose increased (2,114) Device issue (1,417) Product use issue (1,076) Intercepted product preparation error (1,033) Wrong technique in product usage process (935) Device leakage (795) Injection site pain (751) Syringe issue (634) Product quality issue (567) Drug ineffective (488)

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 DEVICE Alternatives Have Lower Hyperhidrosis Risk?

DEVICE vs DEXAMETHASONE DEVICE vs DEXAMETHASONE\DEXAMETHASONE DEVICE vs DEXAMETHASONE\NEOMYCIN DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B DEVICE vs DEXAMETHASONE\TOBRAMYCIN

Related Pages

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