Does UNSPECIFIED INGREDIENT Cause Fluid retention? 85 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 85 reports of Fluid retention have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.3% of all adverse event reports for UNSPECIFIED INGREDIENT.
85
Reports of Fluid retention with UNSPECIFIED INGREDIENT
0.3%
of all UNSPECIFIED INGREDIENT reports
32
Deaths
50
Hospitalizations
How Dangerous Is Fluid retention From UNSPECIFIED INGREDIENT?
Of the 85 reports, 32 (37.6%) resulted in death, 50 (58.8%) required hospitalization, and 24 (28.2%) were considered life-threatening.
Is Fluid retention Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 85 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 Fluid retention?
AMBRISENTAN (3,927)
TREPROSTINIL (3,804)
MACITENTAN (2,861)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,233)
SACUBITRIL\VALSARTAN (2,187)
ADALIMUMAB (1,193)
SELEXIPAG (1,044)
FUROSEMIDE (1,020)
LENALIDOMIDE (1,007)
EPOPROSTENOL (929)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Fluid retention Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN