Does CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE Cause Product administration interrupted? 1,446 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,446 reports of Product administration interrupted have been filed in association with CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE. This represents 19.5% of all adverse event reports for CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE.
How Dangerous Is Product administration interrupted From CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE?
Of the 1,446 reports, 9 (0.6%) resulted in death, 362 (25.0%) required hospitalization, and 4 (0.3%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE. However, 1,446 reports have been filed with the FAERS database.