DEXTROSE MONOHYDRATE

N/A

Manufactured by BECTON DICKINSON AND COMPANY

28,872 FDA adverse event reports analyzed

Last updated: 2026-04-14

About DEXTROSE MONOHYDRATE

DEXTROSE MONOHYDRATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by BECTON DICKINSON AND COMPANY. The most commonly reported adverse reactions for DEXTROSE MONOHYDRATE include MYELOSUPPRESSION, OFF LABEL USE, NAUSEA, DRUG INEFFECTIVE, VOMITING. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for DEXTROSE MONOHYDRATE.

Top Adverse Reactions

MYELOSUPPRESSION1,438 reports
OFF LABEL USE914 reports
NAUSEA877 reports
DRUG INEFFECTIVE846 reports
VOMITING818 reports
ACUTE KIDNEY INJURY760 reports
WHITE BLOOD CELL COUNT DECREASED649 reports
PYREXIA614 reports
DYSPNOEA594 reports
SEPSIS522 reports
HYPOTENSION485 reports
ABDOMINAL PAIN478 reports
NEUTROPHIL COUNT DECREASED457 reports
PRODUCT USE IN UNAPPROVED INDICATION432 reports
DIARRHOEA429 reports
CONDITION AGGRAVATED420 reports
PNEUMONIA411 reports
HYPONATRAEMIA406 reports
ANAEMIA403 reports
DEATH376 reports
MATERNAL EXPOSURE DURING PREGNANCY373 reports
CONSTIPATION361 reports
HYPOGLYCAEMIA361 reports
ASTHENIA350 reports
FATIGUE329 reports
GENERAL PHYSICAL HEALTH DETERIORATION327 reports
ABDOMINAL DISTENSION322 reports
PRURITUS314 reports
ASCITES312 reports
PLATELET COUNT DECREASED306 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME301 reports
CARDIOGENIC SHOCK294 reports
HEADACHE292 reports
RENAL FAILURE281 reports
HYPERTENSION270 reports
PAIN269 reports
DIZZINESS266 reports
RASH262 reports
DRUG HYPERSENSITIVITY246 reports
SOMNOLENCE244 reports
STRESS241 reports
DECREASED APPETITE240 reports
VENTRICULAR FIBRILLATION240 reports
THROMBOCYTOPENIA236 reports
TOXICITY TO VARIOUS AGENTS234 reports
PREMATURE DELIVERY231 reports
FOETAL EXPOSURE DURING PREGNANCY229 reports
CHRONIC KIDNEY DISEASE226 reports
APPENDICITIS223 reports
MALAISE223 reports
APPENDICOLITH216 reports
RESPIRATORY FAILURE214 reports
PREMATURE BABY210 reports
END STAGE RENAL DISEASE206 reports
TACHYCARDIA203 reports
COUGH201 reports
SWELLING199 reports
HYPERKALAEMIA192 reports
PULMONARY EMBOLISM186 reports
HEPATIC FUNCTION ABNORMAL183 reports
CARDIAC ARREST177 reports
CHEST DISCOMFORT175 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE175 reports
DRUG INTERACTION173 reports
DRY MOUTH173 reports
DIABETES MELLITUS170 reports
FALL169 reports
DRUG INTOLERANCE168 reports
PLEURAL EFFUSION168 reports
HYPOKALAEMIA167 reports
BLOOD PHOSPHORUS INCREASED165 reports
DYSPHAGIA165 reports
OEDEMA PERIPHERAL165 reports
BACTERIAL INFECTION163 reports
DEHYDRATION163 reports
CHILLS158 reports
BLOOD CREATININE INCREASED157 reports
HYPOXIA157 reports
THROMBOSIS156 reports
INTENTIONAL PRODUCT MISUSE155 reports
RENAL IMPAIRMENT154 reports
HYPERGLYCAEMIA152 reports
MYASTHENIA GRAVIS152 reports
ERYTHEMA150 reports
INCORRECT ROUTE OF PRODUCT ADMINISTRATION147 reports
HYPOPHOSPHATAEMIA146 reports
HAEMOGLOBIN DECREASED145 reports
URINARY TRACT INFECTION141 reports
HYPERHIDROSIS140 reports
NEURALGIA139 reports
ATRIAL FIBRILLATION138 reports
ARTHRALGIA137 reports
FEBRILE NEUTROPENIA137 reports
METABOLIC ACIDOSIS136 reports
NEUTROPENIA135 reports
ASPARTATE AMINOTRANSFERASE INCREASED134 reports
BLOOD CHOLESTEROL INCREASED132 reports
BLOOD URIC ACID INCREASED132 reports
HYPERPHOSPHATAEMIA132 reports
LACTIC ACIDOSIS132 reports

Report Outcomes

Out of 12,135 classified reports for DEXTROSE MONOHYDRATE:

Serious 92.4%Non-Serious 7.6%

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

Female5,722 (54.1%)
Male4,839 (45.7%)
Unknown25 (0.2%)

Reports by Age

Age 80339 reports
Age 62205 reports
Age 67199 reports
Age 72199 reports
Age 57192 reports
Age 55191 reports
Age 66187 reports
Age 69186 reports
Age 58183 reports
Age 59182 reports
Age 53179 reports
Age 64178 reports
Age 54177 reports
Age 61177 reports
Age 68177 reports
Age 60176 reports
Age 63175 reports
Age 76175 reports
Age 56173 reports
Age 70172 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?

This profile reflects 28,872 FDA FAERS reports that mention DEXTROSE MONOHYDRATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for DEXTROSE MONOHYDRATE?

Frequently reported terms in FAERS include MYELOSUPPRESSION, OFF LABEL USE, NAUSEA, DRUG INEFFECTIVE, VOMITING, ACUTE KIDNEY INJURY. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures DEXTROSE MONOHYDRATE?

Labeling and FAERS entries often list BECTON DICKINSON AND COMPANY in connection with DEXTROSE MONOHYDRATE. 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.