GELOFUSINE

This brand name is authorized in Austria, Estonia, Finland, France, Ireland, Lithuania, Malta, Netherlands, New Zealand, Romania, Singapore.

Active ingredients

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

1	Succinylated gelatin UNII 2G86QN327L - GELATIN, UNSPECIFIED
	Gelatin is a colloidal plasma substitute. When used in the treatment of hypovolaemia gelatin produces significant increases in blood volume, cardiac output, stroke volume, blood pressure, urinary output and oxygen delivery. Gelatin promotes osmotic diuresis, thereby helping to protect the kidneys from the adverse effects of hypovolaemia.
	Read more about Gelatin
2	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 more about Sodium chloride
3	Caustic soda UNII 55X04QC32I - SODIUM HYDROXIDE
	Read more about Caustic soda

Medicine classification

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

ATC Group		Classification
B05AA06	Gelatin agents	B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05A Blood and related products → B05AA Blood substitutes and plasma protein fractions
Discover more medicines within B05AA06

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1032512
FI	Lääkealan turvallisuus- ja kehittämiskeskus	058701
FR	Base de données publique des médicaments	60186552
HK	Department of Health Drug Office	36310, 47624
LT	Valstybinė vaistų kontrolės tarnyba	1010449
MT	Medicines Authority	AA223/00303
NL	Z-Index G-Standaard	14290316, 14616653
NL	Z-Index G-Standaard, PRK	47074
NZ	Medicines and Medical Devices Safety Authority	8208
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W01736002
SG	Health Sciences Authority	08166P