This brand name is authorized in United States
The drug IMUFLEX contains a combination of these active pharmaceutical ingredients (APIs):
1
Glucose
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. |
2
Sodium citrate
UNII B22547B95K - TRISODIUM CITRATE DIHYDRATE
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Sodium citrate has no relevant pharmacodynamic activity other than that caused by its alkalinity (e.g. its gastric acid neutralising capacity). Sodium citrate is a non-particulate antacid for use by mouth to prior to general anaesthesia for caesarean section. |
3
Citric acid
UNII XF417D3PSL - ANHYDROUS CITRIC ACID
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Potassium citrate is indicated for the management of renal tubular acidosis with calcium stones, hypocitraturic calcium oxalate nephrolithiasis of any etiology, uric acid lithiasis with or without calcium stones. When potassium citrate is given orally, the metabolism of absorbed citrate produces an alkaline load. The induced alkaline load in turn increases urinary pH and raises urinary citrate by augmenting citrate clearance without measurably altering ultrafilterable serum citrate. Thus, potassium citrate therapy appears to increase urinary citrate principally by modifying the renal handling of citrate, rather than by increasing the filtered load of citrate. |
4
Sodium phosphate
UNII 3980JIH2SW - SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM
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This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
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Country: US | FDA, National Drug Code | Identifier(s): 53877-010 |
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