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Sodium Citrate

Published: July 26, 2026Updated: July 26, 2026

Sodium Citrate is an anticoagulant solution used primarily in blood collection and extracorporeal circuits such as dialysis and apheresis procedures. It works by binding free calcium in the blood, which is an essential cofactor required for multiple steps in the clotting cascade. This medication is not typically used for systemic anticoagulation in patients but rather for preventing clot formation in blood products and medical equipment.

Quick summary

Sodium Citrate is an anticoagulant used during blood collection and extracorporeal procedures to prevent clotting by binding calcium in the blood.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
B05CB02
RxNorm
56466
Generic
Sodium Citrate
Class
atc-b05
Brands
Cytra 2, Cytra-3, Oracit, Regiocit, Emetrol Chewables, Emetrol Powder, BSS Ophthalmic Solution
Availability
rx
Lactation
unknown
Routes
ophthalmic, oral
Forms
injection, solution, tablet
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity in adults - amounts exceeding 10-20 grams may lead to significant metabolic alkalosis
Chronic overdose: Prolonged use leading to metabolic alkalosis and electrolyte imbalances including hypernatremia and hypokalemia
Immediate actions
Discontinue medication, gastric lavage if ingestion recent, monitor vital signs and electrolytes, intravenous fluids
Antidote
No specific antidote exists - treatment is supportive and symptomatic(Supportive care is effective when initiated promptly)
Poison Control: 1-800-222-1222

Special Populations

9 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

avoid use during pregnancy unless clearly needed, discuss risks and benefits with healthcare provider

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use only when clearly indicated, monitor fluid and electrolyte balance

Monitor

regular prenatal monitoring, electrolyte checks

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use only when clearly indicated, monitor for metabolic alkalosis

Monitor

regular prenatal monitoring, electrolyte and acid-base balance checks

Use with caution and monitor for adverse effects.

✓

lactation

breastfeeding
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

generally considered compatible with breastfeeding

Monitor

no specific monitoring required

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

dose adjustment may be needed based on renal function

Key Recommendations

use with caution, monitor renal function and electrolytes regularly

Monitor

regular renal function tests, electrolyte monitoring

Use with caution and monitor for adverse effects.

✓

pediatric_age

children
safe
FDA Category
N
Dose Adjustment

dose based on weight and clinical indication

Key Recommendations

use under medical supervision, appropriate for pediatric use

Monitor

monitor electrolytes and acid-base balance

⚠

renal_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

monitor renal function, may need dose adjustment

Key Recommendations

use with caution, monitor electrolytes and fluid balance

Monitor

regular renal function tests, electrolyte monitoring

Use with caution and monitor for adverse effects.

✗

renal_impairment

severe
unsafe
FDA Category
N
Dose Adjustment

avoid or use with extreme caution at reduced doses

Key Recommendations

avoid use in severe renal impairment due to risk of sodium overload and metabolic alkalosis

Monitor

frequent renal function and electrolyte monitoring if use is necessary

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

use with caution, no specific dose adjustment guidelines

Key Recommendations

use with caution in severe hepatic impairment, monitor acid-base balance

Monitor

monitor liver function tests and electrolytes

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:Alkalinizing agent, Urinary alkalizer, Anticoagulant

Pharmacological classification of Sodium Citrate

usageMedical guidelines
2023

Common therapeutic uses

Value:Treatment of metabolic acidosis, Urinary alkalinization, Anticoagulation for blood transfusions, Renal tubular acidosis

Primary therapeutic applications

mechanismFDA
2023

Mechanism of action

Value:Buffer system - neutralizes acid and increases plasma bicarbonate, raising urinary pH

Pharmacodynamic properties

formulationsFDA
2023

Available formulations

Value:Oral solution, Intravenous, Ophthalmic solution (BSS)

Dosage forms and formulations

Used during blood transfusion and collection to prevent clotting of donated blood, in hemodialysis circuits to prevent clot formation on dialysis membranes, and in apheresis procedures where blood components are separated and collected outside the body.

Sodium citrate binds ionized (free) calcium in the blood, making it unavailable for the coagulation cascade. Since calcium is required as a cofactor for several enzymatic steps in clot formation, temporarily removing it from circulation prevents blood from clotting while it is outside the body or passing through medical equipment.

This medication is administered directly into blood collection lines or extracorporeal circuits, not given systemically to patients. In procedures where large volumes are used, citrate toxicity can cause hypocalcemia with symptoms such as numbness, tingling, muscle cramps, or in severe cases, cardiac arrhythmias. Patients undergoing prolonged apheresis may require calcium supplementation.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy