Does UNSPECIFIED INGREDIENT Cause Hyponatraemia? 259 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 259 reports of Hyponatraemia have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.0% of all adverse event reports for UNSPECIFIED INGREDIENT.
259
Reports of Hyponatraemia with UNSPECIFIED INGREDIENT
1.0%
of all UNSPECIFIED INGREDIENT reports
135
Deaths
192
Hospitalizations
How Dangerous Is Hyponatraemia From UNSPECIFIED INGREDIENT?
Of the 259 reports, 135 (52.1%) resulted in death, 192 (74.1%) required hospitalization, and 92 (35.5%) were considered life-threatening.
Is Hyponatraemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 259 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 Hyponatraemia?
FUROSEMIDE (3,127)
HYDROCHLOROTHIAZIDE (2,138)
OMEPRAZOLE (1,635)
LANSOPRAZOLE (1,416)
SERTRALINE (1,332)
RAMIPRIL (1,178)
SPIRONOLACTONE (1,166)
PANTOPRAZOLE (1,134)
INDAPAMIDE (976)
AMLODIPINE (879)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Hyponatraemia Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN