HEMOSOL

This brand name is authorized in Estonia, Spain, Finland, France, Croatia, Ireland, Lithuania, New Zealand, United Kingdom, South Africa

Active ingredients

The drug HEMOSOL contains a combination of these active pharmaceutical ingredients (APIs):

1 Sodium chloride
UNII 451W47IQ8X - SODIUM CHLORIDE

Sodium chloride is the principle salt involved in maintaining the osmotic tension of blood and tissues. Changes in osmotic tension influence the movement of fluids and diffusion of salts in cellular tissue.

Read about Sodium chloride
2 Sodium hydrogen carbonate
UNII 8MDF5V39QO - SODIUM BICARBONATE

Sodium bicarbonate has antacid properties. Sodium bicarbonate causes neutralisation of gastric acid with the production of carbon dioxide.

Read about Sodium bicarbonate
3 Calcium chloride
UNII M4I0D6VV5M - CALCIUM CHLORIDE

Calcium is the most abundant mineral in the body, and is an essential body electrolyte. Homeostasis is mainly regulated by the parathyroid hormone, by calcitonin, and by the activated form of vitamin D. Calcium is a structural component of bones and teeth. It is also required for blood clotting, neurotransmitter release, muscle contraction and normal heartbeat.

Read about Calcium chloride
4 Magnesium chloride
UNII 02F3473H9O - MAGNESIUM CHLORIDE
Read about Magnesium chloride
5 Lactic acid
UNII 33X04XA5AT - LACTIC ACID, UNSPECIFIED FORM
Read about Lactic acid

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
HEMOSOL B0 Solution for haemodialysis / haemofiltration Health Products Regulatory Authority (IE) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
B05ZB Hemofiltrates B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05Z Hemodialytics and hemofiltrates
Discover more medicines within B05ZB

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1421424
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 62900
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 048770
Country: FR Base de données publique des médicaments Identifier(s): 61475677
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 325120
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-037692627
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1038226
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 14426
Country: ZA Health Products Regulatory Authority Identifier(s): 50/32.11/1074

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