Does UNSPECIFIED INGREDIENT Cause Hyperhidrosis? 164 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 164 reports of Hyperhidrosis have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.6% of all adverse event reports for UNSPECIFIED INGREDIENT.
164
Reports of Hyperhidrosis with UNSPECIFIED INGREDIENT
0.6%
of all UNSPECIFIED INGREDIENT reports
10
Deaths
52
Hospitalizations
How Dangerous Is Hyperhidrosis From UNSPECIFIED INGREDIENT?
Of the 164 reports, 10 (6.1%) resulted in death, 52 (31.7%) required hospitalization, and 13 (7.9%) 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 UNSPECIFIED INGREDIENT. However, 164 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
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 UNSPECIFIED INGREDIENT Alternatives Have Lower Hyperhidrosis Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN