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Cysteine

Generic Medicine Info
Indications and Dosage
Intravenous
Additive in total parenteral nutrition
Adult: As additive to amino acid solutions to meet the nutritional requirement in patients with severe liver disease who may have impaired enzymatic processes and require TPN: For stable and critically ill patients: 7 mg cysteine hydrochloride/g of amino acids (equivalent to 4.8 mg cysteine/g of amino acids) daily. Doses are given as an admixture into parenteral nutrition solutions; then the resulting solution is given via IV infusion into a central or peripheral vein depending on the osmolarity. Solutions with osmolarity of ≥900 milliosmole/L must be infused via a central catheter. Individualise dose based on patient's clinical condition, daily protein (amino acids) or nutritional/fluid requirements, weight, and additional energy given via oral or enteral route.
Child: As additive to amino acid solutions to meet the nutritional requirements in infants requiring TPN, and in children with severe liver disease who may have impaired enzymatic processes and require TPN: Infants Usual dose: 30-40 mg cysteine hydrochloride/g of amino acids daily; a low dose of 20 mg cysteine hydrochloride/g of amino acids daily may be sufficient. Alternatively, 22 mg cysteine hydrochloride/g of amino acids (equivalent to 15 mg cysteine/g of amino acids) daily. 1-11 years 22 mg cysteine hydrochloride/g of amino acids (equivalent to 15 mg cysteine/g of amino acids) daily. ≥12 years 7 mg cysteine hydrochloride/g of amino acids (equivalent to 4.8 mg cysteine/g of amino acids) daily. Doses are given as an admixture into parenteral nutrition solutions; then the resulting solution is given via IV infusion into a central or peripheral vein depending on the osmolarity. Solutions with osmolarity of ≥900 milliosmole/L must be infused via a central catheter. Individualise dose based on patient's clinical condition, daily protein (amino acids) or nutritional/fluid requirements, weight, and additional energy given via oral or enteral route. Dosage recommendations may vary between local guidelines (refer to institution-specific protocols).
Contraindications
Inborn errors of amino acid metabolism, pulmonary oedema or acidosis due to low cardiac output.
Special Precautions
Patient with cardiac insufficiency, diabetes (including prediabetic patients), pulmonary disease. Correct severe fluid, electrolyte, and acid-base disorders before administration. Not for direct IV infusion. Renal and hepatic impairment. Neonates, infants and children. Pregnancy and lactation.
Adverse Reactions
Significant: Hepatobiliary disorders (e.g. cholecystitis, cholelithiasis, cholestasis, cirrhosis, hepatic steatosis, fibrosis) which may lead to hepatic failure; increased BUN (particularly in patients with renal or hepatic impairment); hyperammonaemia (particularly in infants and patients with hepatic impairment); serum amino acid imbalances, metabolic alkalosis, prerenal azotaemia, stupor, and coma (especially in patients with hepatic impairment); metabolic acidosis (in preterm infants); vein irritation/damage or thrombosis (if hypertonic nutritional solutions are given via peripheral vein).
Gastrointestinal disorders: Nausea.
General disorders and administration site conditions: Fever, infusion site reactions (e.g. erythema, phlebitis, thrombosis, warm sensation).
Vascular disorders: Flushing.
Monitoring Parameters
Monitor fluid and electrolyte status, blood glucose, kidney and liver functions, CBC and coagulation parameters; blood ammonia levels (if hepatic impairment is present), triglycerides (if adding lipid emulsion), acid-base balance, serum proteins, blood culture, urine osmolarity and glucose, nitrogen intake.
Lab Interference
May interfere with estimations of nitrogen-containing substances. May cause a false-positive result with the nitroprusside test for ketone bodies.
Action
Description:
Mechanism of Action: Cysteine is a non-essential amino acid. Endogenously, it is synthesised from methionine by cystathionase via the trans-sulfuration pathway and serves as a precursor substrate for glutathione and taurine. As an exogenous source, it provides cysteine to the systemic circulation of patients who cannot synthesise adequate quantities due to deficient or insufficient cystathionase activity.
Synonym(s): L-cysteine.
Chemical Structure

Chemical Structure Image
Cysteine

Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 5862, L-(+)-Cysteine. https://pubchem.ncbi.nlm.nih.gov/compound/L-_-Cysteine. Accessed Feb. 25, 2026.

Storage
Store between 15-30°C. Protect from light and excessive heat.
MIMS Class
Supplements & Adjuvant Therapy
References
Brayfield A, Cadart C (eds). Cysteine. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 10/02/2026.

Cysteine. Gold Standard Drug Database in ClinicalKey [online]. Elsevier Inc. https://www.clinicalkey.com. Accessed 10/02/2026.

Cysteine. UpToDate Lexidrug, Lexi-Drugs Multinational Online. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 10/02/2026.

Cysteine. UpToDate Lexidrug, Pediatric and Neonatal Lexi-Drugs Online. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 10/02/2026.

Elcys Injection, Solution (Exela Pharma Sciences, LLC). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 10/02/2026.

Elcys Injection, Solution (Exela Pharma Sciences, LLC). U.S. FDA. https://www.fda.gov. Accessed 01/10/2020.

L-cysteine Hydrochloride Injection, Solution (Sandoz Inc.). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 01/10/2020.

Disclaimer: This information is independently developed by MIMS based on Cysteine from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to MIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, MIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2026 MIMS. All rights reserved. Powered by MIMS.com
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