This brand name is authorized in Croatia, Ireland, Lithuania, Malta, New Zealand, Poland, Romania, Spain, Tunisia, Turkey, UK.
The drug DIANEAL PD4 contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
LX22YL083G - DEXTROSE MONOHYDRATE
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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. |
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2
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UNII
451W47IQ8X - SODIUM CHLORIDE
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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. |
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3
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UNII
TU7HW0W0QT - SODIUM LACTATE
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4
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UNII
M4I0D6VV5M - CALCIUM CHLORIDE
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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. |
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5
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UNII
02F3473H9O - MAGNESIUM CHLORIDE
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| B05DB | Hypertonic solutions | B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05D Peritoneal dialytics |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| ES | Centro de información online de medicamentos de la AEMPS | 60050, 60051, 60053, 60054 |
| GB | Medicines & Healthcare Products Regulatory Agency | 170457, 170470, 170484, 170488, 170492, 170498, 170510, 170522, 170534, 388541, 388542, 388603, 388604, 388607, 388608, 388610, 388612 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-152351700, HR-H-793742019, HR-H-884218077 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1013848, 1013849, 1013850, 1013851, 1013852, 1013853, 1013854, 1013855, 1013856, 1013857, 1013858, 1013859, 1034421, 1034422, 1034423 |
| MT | Medicines Authority | MA1277/01001, MA1277/01002, MA1277/01003 |
| NZ | Medicines and Medical Devices Safety Authority | 14828, 14829, 14830, 15784, 7259, 7264, 7268 |
| PL | Rejestru Produktów Leczniczych | 100116834, 100116857, 100116886 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | 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 |
| TN | Direction de la Pharmacie et du Médicament | 10193031H, 10193032H, 10193033H, 10193034H, 10193035H |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681413880735, 8681413880742, 8681413880759, 8681413880766, 8681413880773, 8681413880780, 8681413880797, 8681413880803, 8681413880810, 8681413880827, 8681413880834, 8681413880841 |
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