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Manufactured by Vantive US Healthcare LLC
11,786 FDA adverse event reports analyzed
Last updated: 2026-04-14
SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Vantive US Healthcare LLC. The most commonly reported adverse reactions for SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE include DEATH, PERITONITIS, MYOCARDIAL INFARCTION, CARDIAC FAILURE CONGESTIVE, SEPSIS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE.
Out of 8,081 classified reports for SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE:
The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.
Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.
This profile reflects 11,786 FDA FAERS reports that mention SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include DEATH, PERITONITIS, MYOCARDIAL INFARCTION, CARDIAC FAILURE CONGESTIVE, SEPSIS, INFECTION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list Vantive US Healthcare LLC in connection with SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE. Always verify the specific product and NDC with your pharmacist.