Nchi: Kanada
Lugha: Kiingereza
Chanzo: Health Canada
METHIONINE; L-ISOLEUCINE; L-VALINE; HISTIDINE; L-THREONINE; SODIUM ACETATE; POTASSIUM PHOSPHATE DIBASIC; SODIUM CHLORIDE; MAGNESIUM CHLORIDE; DEXTROSE; L-LEUCINE; L-PHENYLALANINE; LYSINE (L-LYSINE HYDROCHLORIDE); TRYPTOPHAN; L-ALANINE; L-ARGININE; L-PROLINE; SERINE; GLYCINE; L-TYROSINE
BAXTER CORPORATION
B05BA10
COMBINATIONS
200MG; 300MG; 290MG; 240MG; 210MG; 205MG; 261MG; 58.5MG; 24MG; 10G; 365MG; 280MG; 290MG; 90MG; 1.04G; 575MG; 340MG; 250MG; 515MG; 20MG
SOLUTION
METHIONINE 200MG; L-ISOLEUCINE 300MG; L-VALINE 290MG; HISTIDINE 240MG; L-THREONINE 210MG; SODIUM ACETATE 205MG; POTASSIUM PHOSPHATE DIBASIC 261MG; SODIUM CHLORIDE 58.5MG; MAGNESIUM CHLORIDE 24MG; DEXTROSE 10G; L-LEUCINE 365MG; L-PHENYLALANINE 280MG; LYSINE (L-LYSINE HYDROCHLORIDE) 290MG; TRYPTOPHAN 90MG; L-ALANINE 1.04G; L-ARGININE 575MG; L-PROLINE 340MG; SERINE 250MG; GLYCINE 515MG; L-TYROSINE 20MG
INTRAVENOUS
2000ML
Ethical
REPLACEMENT PREPARATIONS
Active ingredient group (AIG) number: 2050850018; AHFS:
APPROVED
1999-03-10
_Product Monograph Master Template _ _Template Date: September 2020 _ _CLINIMIX E (Blend C) _ _Page 1 of 31_ PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION INFORMATION CLINIMIX E Amino Acids with Electrolytes in Dextrose Injection 5% Amino Acids (Blend C) with Electrolytes in 10% Dextrose Injection 5% Amino Acids (Blend C) with Electrolytes in 16.6% Dextrose Injection Solution for Infusion, Intravenous Intravenous Nutritive Supplements Baxter Corporation Mississauga, Ontario L5N 0C2 Date of Initial Authorization: DEC 31, 1993 Date of Revision: MAR 31, 2022 Submission Control Number: 256758 Baxter, Clinimix, Clarity and Travasol are registered trademarks of Baxter International Inc. _ _ _Product Monograph Master Template _ _Template Date: September 2020 _ _CLINIMIX E (Blend C) _ _Page 2 of 31_ RECENT MAJOR LABEL CHANGES 6 Warnings and Precautions 04/2020 3 Dosage and Administration 08/2020 6 Warnings and Precautions 08/2020 TABLE OF CONTENTS SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF AUTHORIZATION ARE NOT LISTED. RECENT MAJOR LABEL CHANGES............................................................................................ 2 TABLE OF CONTENTS .............................................................................................................. 2 PART I: HEALTH PROFESSIONAL INFORMATION ..................................................................... 4 1 INDICATIONS .............................................................................................................. 4 1.1 Pediatrics .......................................................................................................... 4 1.2 Geriatrics........................................................................................................... 4 2 CONTRAINDICATIONS ................................................................................................. 4 4 DOSAGE AND ADMINISTRATION................................................................................. 5 4.1 Dosing Considerations .... Soma hati kamili