Страна: Канада
Язык: английский
Источник: Health Canada
SODIUM CHLORIDE; SODIUM LACTATE; CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; ICODEXTRIN
BAXTER CORPORATION
B05DA
ISOTONIC SOLUTIONS
5.35G; 4.48G; 257MG; 51MG; 75G
SOLUTION
SODIUM CHLORIDE 5.35G; SODIUM LACTATE 4.48G; CALCIUM CHLORIDE 257MG; MAGNESIUM CHLORIDE 51MG; ICODEXTRIN 75G
HAEMODIALYSIS (INTRAPERITONEAL)
2/2.5/3L
Ethical
HEMODIALYSIS SOLUTION
Active ingredient group (AIG) number: 0538301002; AHFS:
APPROVED
1999-09-17
_ _ _EXTRANEAL (icodextrin, sodium chloride, sodium lactate, calcium chloride, magnesium chloride) _ _Page 1 of 29 _ PRODUCT MONOGRAPH EXTRANEAL Icodextrin, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride 75 g/L Icodextrin 5.35 g/L Sodium Chloride 4.48 g/L Sodium Lactate 257 mg/L Calcium Chloride 51 mg/L Magnesium Chloride Peritoneal Dialysis Solution BAXTER CORPORATION Mississauga, Ontario L5N 0C2 Control Number: 195522 Date of Revision: September 27, 2016 Baxter, Extraneal, and Viaflex are trademarks of Baxter International Inc. _ _ _EXTRANEAL (icodextrin, sodium chloride, sodium lactate, calcium chloride, magnesium chloride) _ _Page 2 of 29 _ TABLE OF CONTENTS PART I: HEALTH PROFESSIONAL INFORMATION .........................................................4 SUMMARY PRODUCT INFORMATION ........................................................................4 INDICATIONS AND CLINICAL USE ..............................................................................4 CONTRAINDICATIONS ...................................................................................................4 WARNINGS AND PRECAUTIONS ..................................................................................5 ADVERSE REACTIONS ................................................................................................... 9 PART III: PATIENT MEDICATION INFORMATION .......................................................26 DOSAGE AND ADMINISTRATION ..............................................................................14 OVERDOSAGE ................................................................................................................15 ACTION AND CLINICAL PHARMACOLOGY ............................................................15 STORAGE AND STABILITY ..........................................................................................16 DOSAGE FORMS, COMPOSITION AND PACKAGING .............................................17 PART II: SCIENTIFIC INFORMATION ................................. Прочитать полный документ