Does MAGNESIUM Cause Recalled product? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Recalled product have been filed in association with MAGNESIUM (citroma). This represents 0.1% of all adverse event reports for MAGNESIUM.
10
Reports of Recalled product with MAGNESIUM
0.1%
of all MAGNESIUM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Recalled product From MAGNESIUM?
Of the 10 reports, 1 (10.0%) required hospitalization.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MAGNESIUM. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does MAGNESIUM Cause?
Drug ineffective (2,160)
Off label use (1,502)
Maternal exposure during pregnancy (1,227)
Pain (1,098)
Nausea (1,084)
Dyspnoea (961)
Product use in unapproved indication (949)
Condition aggravated (926)
Vomiting (912)
Diarrhoea (900)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which MAGNESIUM Alternatives Have Lower Recalled product Risk?
MAGNESIUM vs MAGNESIUM ASPARTATE
MAGNESIUM vs MAGNESIUM ASPARTATE\POTASSIUM ASPARTATE
MAGNESIUM vs MAGNESIUM HYDROXIDE
MAGNESIUM vs MAGNESIUM OROTATE
MAGNESIUM vs MAGNESIUM SALICYLATE