GELOPLASMA

This brand name is authorized in Estonia, Ireland, Lithuania, Netherlands, Poland, Romania, Spain.

Active ingredients

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

1
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
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
UNII 02F3473H9O - MAGNESIUM CHLORIDE
 
Read more about Magnesium chloride
4
UNII 660YQ98I10 - POTASSIUM CHLORIDE
 

Potassium plays a vital physiological role in maintenance of normal electrical excitability of nerve and muscle. It is also important in the genesis and correction of imbalances of acid-base metabolism.

 
Read more about Potassium chloride
5
UNII TU7HW0W0QT - SODIUM LACTATE
 
Read more about Lactic acid

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 1223402, 1274633, 1482791
ES Centro de información online de medicamentos de la AEMPS 68045
LT Valstybinė vaistų kontrolės tarnyba 1022257, 1024733, 1055895
NL Z-Index G-Standaard 14794497
NL Z-Index G-Standaard, PRK 67067
PL Rejestru Produktów Leczniczych 100163845
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W62082001, W62082002, W62082003

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