Does UNSPECIFIED INGREDIENT Cause Hypomagnesaemia? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Hypomagnesaemia have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
32
Reports of Hypomagnesaemia with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
4
Deaths
22
Hospitalizations
How Dangerous Is Hypomagnesaemia From UNSPECIFIED INGREDIENT?
Of the 32 reports, 4 (12.5%) resulted in death, 22 (68.8%) required hospitalization, and 3 (9.4%) were considered life-threatening.
Is Hypomagnesaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 32 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 Hypomagnesaemia?
OMEPRAZOLE (1,766)
PANTOPRAZOLE (1,246)
PANITUMUMAB (611)
ESOMEPRAZOLE (591)
CARBOPLATIN (586)
LANSOPRAZOLE (504)
FUROSEMIDE (501)
FLUOROURACIL (477)
METFORMIN (415)
CISPLATIN (395)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Hypomagnesaemia Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN