MULTIBIC

This brand name is authorized in Austria, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Lithuania, Singapore, Spain, Turkey, UK.

Active ingredients

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

1
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 more about Calcium chloride
2
UNII LX22YL083G - DEXTROSE MONOHYDRATE
 

Glucose is frequently used in both adults and children to restore blood glucose concentrations in the treatment of hypoglycaemia resulting from insulin excess or from other causes. The metabolism of glucose is an energy source for the body.

 
Read more about Glucose
3
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
4
UNII 02F3473H9O - MAGNESIUM CHLORIDE
 
Read more about Magnesium chloride
5
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
6
UNII 8MDF5V39QO - SODIUM BICARBONATE
 

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

 
Read more about Sodium bicarbonate

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 MULTIBIC Solution for haemodialysis/haemofiltration MPI, EU: SmPC Marketing Authorisation Holder

Medicine classification

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

ATC Group 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)
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 4360-MEE-0818, 4361-MEE-0818, 4372-MEE-0918
EE Ravimiamet 1434136, 1434147, 1434158
ES Centro de información online de medicamentos de la AEMPS 65804, 65814, 65815
FI Lääkealan turvallisuus- ja kehittämiskeskus 072990, 073025
FR Base de données publique des médicaments 63515348, 68604270
GB Medicines & Healthcare Products Regulatory Agency 350635, 350815, 350824, 350830
HR Agencija za lijekove i medicinske proizvode HR-H-472471676
LT Valstybinė vaistų kontrolės tarnyba 1054901, 1054902, 1054903
SG Health Sciences Authority 14061P
TR İlaç ve Tıbbi Cihaz Kurumu 8699684675028, 8699684675035, 8699684675042, 8699684675127, 8699684675134, 8699684675141

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