DIANEAL PD4

This brand name is authorized in Spain, Croatia, Ireland, Lithuania, Malta, New Zealand, Poland, Romania, Tunisia, Turkey, United Kingdom

Active ingredients

The drug DIANEAL PD4 contains a combination of these active pharmaceutical ingredients (APIs):

1 Glucose anhydrous
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 about Glucose
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 about Sodium chloride
3 Lactic acid
UNII TU7HW0W0QT - SODIUM LACTATE
Read about Lactic acid
4 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
5 Magnesium chloride
UNII 02F3473H9O - MAGNESIUM CHLORIDE
Read about Magnesium chloride

Medicine classification

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

ATC code Group title Classification
B05DB Hypertonic solutions B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05D Peritoneal dialytics
Discover more medicines within B05DB

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 60050, 60051, 60053, 60054
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 170457, 170470, 170484, 170488, 170492, 170498, 170510, 170522, 170534, 388541, 388542, 388603, 388604, 388607, 388608, 388610, 388612
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-152351700, HR-H-793742019, HR-H-884218077
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1013848, 1013849, 1013850, 1013851, 1013852, 1013853, 1013854, 1013855, 1013856, 1013857, 1013858, 1013859, 1034421, 1034422, 1034423
Country: MT Medicines Authority Identifier(s): MA1277/01001, MA1277/01002, MA1277/01003
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 14828, 14829, 14830, 15784, 7259, 7264, 7268
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100116834, 100116857, 100116886
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W10051008, W10051009, W10051010, W10051011, W10051012, W10051013, W10051014, W10051015, W10051016, W10051017, W10051018, W10051019, W10058008, W10058009, W10058010, W10058011, W10058012, W10058013, W10058014, W10058015, W10058016, W10058017, W10058018, W10058019, W10065008, W10065009, W10065010, W10065011, W10065012, W10065013, W10065014, W10065015, W10065016, W10065017, W10065018, W10065019
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 10193031H, 10193032H, 10193033H, 10193034H, 10193035H
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8681413880735, 8681413880742, 8681413880759, 8681413880766, 8681413880773, 8681413880780, 8681413880797, 8681413880803, 8681413880810, 8681413880827, 8681413880834, 8681413880841

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