CALCIUM CHLORIDE

N/A

Manufactured by American Regent, Inc.

15,604 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CALCIUM CHLORIDE

CALCIUM CHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by American Regent, Inc.. The most commonly reported adverse reactions for CALCIUM CHLORIDE include PAIN, INJURY, DRUG INEFFECTIVE, NAUSEA, ANXIETY. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CALCIUM CHLORIDE.

Top Adverse Reactions

PAIN416 reports
INJURY400 reports
DRUG INEFFECTIVE374 reports
NAUSEA310 reports
ANXIETY288 reports
OFF LABEL USE284 reports
RENAL FAILURE264 reports
PYREXIA257 reports
HYPOTENSION228 reports
DYSPNOEA220 reports
UNEVALUABLE EVENT206 reports
PEMPHIGUS205 reports
PNEUMONIA204 reports
JOINT SWELLING203 reports
CONDITION AGGRAVATED200 reports
DEATH197 reports
OEDEMA192 reports
PAIN IN EXTREMITY187 reports
FEAR185 reports
URTICARIA185 reports
VOMITING183 reports
FATIGUE180 reports
SLEEP DISORDER179 reports
TYPE 2 DIABETES MELLITUS179 reports
MOBILITY DECREASED176 reports
HYPERTENSION175 reports
DRUG HYPERSENSITIVITY172 reports
RENAL IMPAIRMENT172 reports
PSORIATIC ARTHROPATHY171 reports
ULCER HAEMORRHAGE171 reports
GAIT DISTURBANCE170 reports
LIVER INJURY170 reports
PERICARDITIS169 reports
RENAL INJURY169 reports
SINUSITIS169 reports
DIARRHOEA168 reports
EMOTIONAL DISTRESS165 reports
INSOMNIA162 reports
HEADACHE160 reports
STRESS159 reports
PRODUCT USE IN UNAPPROVED INDICATION156 reports
GENERAL PHYSICAL HEALTH DETERIORATION152 reports
STOMATITIS152 reports
ARTHRALGIA149 reports
WEIGHT INCREASED144 reports
DYSPEPSIA143 reports
HYPERSENSITIVITY143 reports
MIGRAINE143 reports
DIZZINESS142 reports
ASTHMA141 reports
DRUG INTOLERANCE141 reports
MULTI ORGAN FAILURE134 reports
SWELLING131 reports
MATERNAL EXPOSURE DURING PREGNANCY130 reports
NASOPHARYNGITIS130 reports
ANHEDONIA129 reports
ABDOMINAL PAIN127 reports
INFUSION RELATED REACTION125 reports
MALAISE125 reports
RASH125 reports
ABDOMINAL PAIN UPPER124 reports
BLISTER124 reports
ALOPECIA123 reports
PRESCRIBED OVERDOSE123 reports
LOWER RESPIRATORY TRACT INFECTION122 reports
DEPRESSION121 reports
CONFUSIONAL STATE120 reports
PRODUCT USE ISSUE120 reports
PULMONARY FIBROSIS120 reports
PRURITUS119 reports
IRRITABLE BOWEL SYNDROME117 reports
MUSCLE INJURY117 reports
RHEUMATOID ARTHRITIS116 reports
LUPUS VULGARIS115 reports
BLOOD CHOLESTEROL INCREASED114 reports
ABDOMINAL DISCOMFORT111 reports
CHEST PAIN111 reports
SYNOVITIS111 reports
THERAPEUTIC RESPONSE DECREASED111 reports
WHEEZING110 reports
RESPIRATORY FAILURE109 reports
HAND DEFORMITY108 reports
PERIPHERAL SWELLING108 reports
THERAPY NON RESPONDER108 reports
GLOSSODYNIA106 reports
LOWER LIMB FRACTURE106 reports
CONTRAINDICATED PRODUCT ADMINISTERED104 reports
DECREASED APPETITE104 reports
LIVER DISORDER104 reports
DUODENAL ULCER PERFORATION103 reports
HELICOBACTER INFECTION103 reports
HEPATIC ENZYME INCREASED103 reports
MUSCULOSKELETAL STIFFNESS103 reports
SYSTEMIC LUPUS ERYTHEMATOSUS103 reports
TREATMENT FAILURE101 reports
DISCOMFORT100 reports
THERAPEUTIC PRODUCT EFFECT DECREASED100 reports
ASTHENIA99 reports
INFECTION99 reports
ANTI CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE98 reports

Report Outcomes

Out of 2,917 classified reports for CALCIUM CHLORIDE:

Serious 90.2%Non-Serious 9.8%

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

Female1,575 (58.9%)
Male1,095 (40.9%)
Unknown6 (0.2%)

Reports by Age

Age 43129 reports
Age 5478 reports
Age 7573 reports
Age 5956 reports
Age 7156 reports
Age 6555 reports
Age 6955 reports
Age 4650 reports
Age 7050 reports
Age 6648 reports
Age 6147 reports
Age 7247 reports
Age 8047 reports
Age 5746 reports
Age 6246 reports
Age 6746 reports
Age 7446 reports
Age 6444 reports
Age 7743 reports
Age 6340 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 CHLORIDE?

This profile reflects 15,604 FDA FAERS reports that mention CALCIUM CHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CALCIUM CHLORIDE?

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

Who manufactures CALCIUM CHLORIDE?

Labeling and FAERS entries often list American Regent, Inc. in connection with CALCIUM 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.