DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE

N/A

Manufactured by Fresenius Medical Care North America

10,365 FDA adverse event reports analyzed

Last updated: 2026-04-14

About DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE

DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Fresenius Medical Care North America. The most commonly reported adverse reactions for DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE include PERITONITIS, PERITONITIS BACTERIAL, ABDOMINAL DISTENSION, ABDOMINAL PAIN, DEATH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE.

Top Adverse Reactions

PERITONITIS1,475 reports
PERITONITIS BACTERIAL897 reports
ABDOMINAL DISTENSION611 reports
ABDOMINAL PAIN416 reports
DEATH328 reports
MALAISE305 reports
DYSPNOEA280 reports
PAIN273 reports
BLOODY PERITONEAL EFFLUENT270 reports
FLUID OVERLOAD267 reports
INFECTION259 reports
DISCOMFORT221 reports
ABDOMINAL DISCOMFORT199 reports
VOMITING182 reports
DIARRHOEA175 reports
CATHETER SITE INFECTION168 reports
TREATMENT NONCOMPLIANCE167 reports
HYPERVOLAEMIA162 reports
CARDIAC ARREST161 reports
NAUSEA152 reports
FLUID RETENTION120 reports
PNEUMONIA112 reports
CONSTIPATION103 reports
HYPOTENSION103 reports
PERIPHERAL SWELLING99 reports
MUSCLE SPASMS88 reports
SWELLING87 reports
SEPSIS86 reports
CHEST PAIN82 reports
HERNIA82 reports
FUNGAL PERITONITIS81 reports
ASTHENIA76 reports
FALL67 reports
MYOCARDIAL INFARCTION65 reports
ARTHRALGIA64 reports
DEVICE OCCLUSION63 reports
DEHYDRATION62 reports
INADEQUATE ASEPTIC TECHNIQUE IN USE OF PRODUCT54 reports
HYPERTENSION53 reports
DIZZINESS51 reports
INGUINAL HERNIA51 reports
WEIGHT INCREASED48 reports
BACK PAIN47 reports
HYPERKALAEMIA47 reports
PULMONARY OEDEMA47 reports
PERITONEAL CLOUDY EFFLUENT45 reports
PLEURAL EFFUSION45 reports
CEREBROVASCULAR ACCIDENT44 reports
OEDEMA PERIPHERAL42 reports
PERITONEAL DIALYSIS COMPLICATION42 reports
DEVICE RELATED INFECTION41 reports
ABDOMINAL HERNIA39 reports
CONFUSIONAL STATE39 reports
FATIGUE39 reports
UMBILICAL HERNIA39 reports
MUSCULOSKELETAL PAIN38 reports
ABDOMINAL PAIN UPPER37 reports
BLOOD PRESSURE INCREASED37 reports
BLOOD PRESSURE ABNORMAL36 reports
BLOOD PRESSURE DECREASED36 reports
FLUID IMBALANCE36 reports
OEDEMA35 reports
STAPHYLOCOCCUS TEST POSITIVE35 reports
PRODUCT DOSE OMISSION ISSUE34 reports
PYREXIA34 reports
AZOTAEMIA33 reports
PAIN IN EXTREMITY33 reports
BLOOD GLUCOSE DECREASED32 reports
URINARY TRACT INFECTION32 reports
CARDIAC FAILURE CONGESTIVE31 reports
BLOOD GLUCOSE INCREASED28 reports
CARDIO RESPIRATORY ARREST28 reports
HYPOKALAEMIA28 reports
ULTRAFILTRATION FAILURE28 reports
MENTAL STATUS CHANGES27 reports
DEVICE MALFUNCTION26 reports
SEIZURE26 reports
STAPHYLOCOCCAL INFECTION25 reports
COMPLICATION ASSOCIATED WITH DEVICE24 reports
ATRIAL FIBRILLATION21 reports
CARDIAC DISORDER21 reports
WEIGHT DECREASED21 reports
ACUTE MYOCARDIAL INFARCTION20 reports
HYPERGLYCAEMIA20 reports
HYPOGLYCAEMIA20 reports
SEPTIC SHOCK20 reports
BURNING SENSATION19 reports
FLATULENCE19 reports
CATHETER SITE PAIN18 reports
DRUG DOSE OMISSION18 reports
HEADACHE18 reports
ILLNESS18 reports
UNRESPONSIVE TO STIMULI18 reports
ANXIETY17 reports
CHEST DISCOMFORT17 reports
JOINT SWELLING17 reports
CATHETER SITE HAEMORRHAGE16 reports
DISORIENTATION16 reports
PRURITUS16 reports
FEELING COLD15 reports

Report Outcomes

Out of 8,484 classified reports for DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE:

Serious 53.1%Non-Serious 46.9%

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 Breakdown

Reports by Sex

Male4,579 (56.4%)
Female3,540 (43.6%)

Reports by Age

Age 6875 reports
Age 6975 reports
Age 7375 reports
Age 6773 reports
Age 7273 reports
Age 6572 reports
Age 7072 reports
Age 7471 reports
Age 7670 reports
Age 7168 reports
Age 6367 reports
Age 5966 reports
Age 6266 reports
Age 7765 reports
Age 6464 reports
Age 5260 reports
Age 6060 reports
Age 6659 reports
Age 5657 reports
Age 5755 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE?

This profile reflects 10,365 FDA FAERS reports that mention DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE?

Frequently reported terms in FAERS include PERITONITIS, PERITONITIS BACTERIAL, ABDOMINAL DISTENSION, ABDOMINAL PAIN, DEATH, MALAISE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE?

Labeling and FAERS entries often list Fresenius Medical Care North America in connection with DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.