CALCIUM GLUCONATE

N/A

Manufactured by WG Critical Care, LLC

80,205 FDA adverse event reports analyzed

Last updated: 2026-04-14

About CALCIUM GLUCONATE

CALCIUM GLUCONATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by WG Critical Care, LLC. The most commonly reported adverse reactions for CALCIUM GLUCONATE include DRUG INEFFECTIVE, PAIN, FATIGUE, OFF LABEL USE, RHEUMATOID ARTHRITIS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CALCIUM GLUCONATE.

Top Adverse Reactions

DRUG INEFFECTIVE2,061 reports
PAIN1,636 reports
FATIGUE1,626 reports
OFF LABEL USE1,522 reports
RHEUMATOID ARTHRITIS1,337 reports
NAUSEA1,309 reports
ALOPECIA1,281 reports
PEMPHIGUS1,204 reports
PSORIATIC ARTHROPATHY1,200 reports
ARTHROPATHY1,196 reports
ABDOMINAL DISCOMFORT1,191 reports
VOMITING1,191 reports
SYSTEMIC LUPUS ERYTHEMATOSUS1,180 reports
DIARRHOEA1,151 reports
GLOSSODYNIA1,135 reports
CONDITION AGGRAVATED1,108 reports
RASH1,100 reports
LIVER INJURY1,077 reports
PYREXIA1,029 reports
HEADACHE1,007 reports
HYPERTENSION988 reports
SWELLING978 reports
ARTHRALGIA966 reports
PRODUCT USE ISSUE960 reports
HAND DEFORMITY936 reports
DYSPNOEA911 reports
DRUG INTOLERANCE904 reports
DIZZINESS897 reports
CONTRAINDICATED PRODUCT ADMINISTERED895 reports
MALAISE881 reports
MATERNAL EXPOSURE DURING PREGNANCY874 reports
DRUG HYPERSENSITIVITY866 reports
JOINT SWELLING860 reports
PNEUMONIA857 reports
WOUND850 reports
SYNOVITIS849 reports
INFUSION RELATED REACTION844 reports
PERICARDITIS827 reports
GENERAL PHYSICAL HEALTH DETERIORATION808 reports
HYPOAESTHESIA807 reports
DISCOMFORT805 reports
ANTI CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE786 reports
ASTHENIA784 reports
MOBILITY DECREASED771 reports
BLOOD CHOLESTEROL INCREASED747 reports
DECREASED APPETITE742 reports
FIBROMYALGIA738 reports
HYPERSENSITIVITY737 reports
RHEUMATOID FACTOR POSITIVE737 reports
HEPATIC ENZYME INCREASED731 reports
NASOPHARYNGITIS727 reports
MUSCULOSKELETAL STIFFNESS710 reports
CONFUSIONAL STATE705 reports
CHEST PAIN704 reports
OEDEMA697 reports
DUODENAL ULCER PERFORATION689 reports
INFECTION686 reports
ABDOMINAL PAIN UPPER685 reports
TYPE 2 DIABETES MELLITUS682 reports
HELICOBACTER INFECTION680 reports
PERIPHERAL SWELLING675 reports
BLISTER668 reports
STOMATITIS660 reports
PRURITUS658 reports
RHEUMATIC FEVER654 reports
WEIGHT INCREASED653 reports
PAIN IN EXTREMITY652 reports
WEIGHT DECREASED648 reports
URTICARIA645 reports
INTENTIONAL PRODUCT USE ISSUE636 reports
INJURY635 reports
WHEEZING632 reports
PRODUCT USE IN UNAPPROVED INDICATION627 reports
ABDOMINAL PAIN625 reports
TREATMENT FAILURE600 reports
LOWER RESPIRATORY TRACT INFECTION596 reports
IRRITABLE BOWEL SYNDROME576 reports
SINUSITIS574 reports
MUSCLE INJURY573 reports
CONTUSION570 reports
SWOLLEN JOINT COUNT INCREASED567 reports
THERAPEUTIC PRODUCT EFFECT DECREASED558 reports
IMPAIRED HEALING541 reports
FOLLICULITIS532 reports
SLEEP DISORDER528 reports
MEMORY IMPAIRMENT517 reports
MUSCLE SPASMS515 reports
PRESCRIBED OVERDOSE499 reports
DYSPEPSIA493 reports
ASTHMA491 reports
PULMONARY FIBROSIS481 reports
OEDEMA PERIPHERAL471 reports
INSOMNIA465 reports
DEPRESSION453 reports
MIGRAINE452 reports
ILL DEFINED DISORDER451 reports
GASTROINTESTINAL DISORDER449 reports
JOINT RANGE OF MOTION DECREASED449 reports
PARAESTHESIA448 reports
GAIT INABILITY446 reports

Report Outcomes

Out of 11,608 classified reports for CALCIUM GLUCONATE:

Serious 81.8%Non-Serious 18.2%

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

Female7,531 (70.1%)
Male3,183 (29.6%)
Unknown22 (0.2%)

Reports by Age

Age 43569 reports
Age 59272 reports
Age 65229 reports
Age 44228 reports
Age 62218 reports
Age 78218 reports
Age 75205 reports
Age 72199 reports
Age 56198 reports
Age 67198 reports
Age 71194 reports
Age 54183 reports
Age 69183 reports
Age 57181 reports
Age 80180 reports
Age 68178 reports
Age 66177 reports
Age 64170 reports
Age 74168 reports
Age 63161 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 CALCIUM GLUCONATE?

This profile reflects 80,205 FDA FAERS reports that mention CALCIUM GLUCONATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CALCIUM GLUCONATE?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, PAIN, FATIGUE, OFF LABEL USE, RHEUMATOID ARTHRITIS, NAUSEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CALCIUM GLUCONATE?

Labeling and FAERS entries often list WG Critical Care, LLC in connection with CALCIUM GLUCONATE. 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.