Does UNSPECIFIED INGREDIENT Cause Dehydration? 281 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 281 reports of Dehydration have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
281
Reports of Dehydration with UNSPECIFIED INGREDIENT
1.1%
of all UNSPECIFIED INGREDIENT reports
37
Deaths
214
Hospitalizations
How Dangerous Is Dehydration From UNSPECIFIED INGREDIENT?
Of the 281 reports, 37 (13.2%) resulted in death, 214 (76.2%) required hospitalization, and 21 (7.5%) were considered life-threatening.
Is Dehydration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 281 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 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 UNSPECIFIED INGREDIENT Alternatives Have Lower Dehydration Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN