Nchi: Marekani
Lugha: Kiingereza
Chanzo: NLM (National Library of Medicine)
LEUCINE (UNII: GMW67QNF9C) (LEUCINE - UNII:GMW67QNF9C), PHENYLALANINE (UNII: 47E5O17Y3R) (PHENYLALANINE - UNII:47E5O17Y3R), LYSINE (UNII: K3Z4F929H6) (LYSINE - UNII:K3Z4F929H6), METHIONINE (UNII: AE28F7PNPL) (METHIONINE - UNII:AE28F7PNPL), ISOLEUCINE (UNII: 04Y7590D77) (ISOLEUCINE - UNII:04Y7590D77), VALINE (UNII: HG18B9YRS7) (VALINE - UNII:HG18B9YRS7), HISTIDINE (UNII: 4QD397987E) (HISTIDINE - UNII:4QD397987E), THREONINE (UNII: 2ZD004190S) (THREONINE - UNII:2ZD004190S), TRYPTOPHAN (UNII: 8DUH1N11BX
Baxter Healthcare Corporation
LEUCINE
LEUCINE 201 mg in 100 mL
INTRAVENOUS
PRESCRIPTION DRUG
CLINIMIX E is indicated as a source of calories, protein, and electrolytes for patients requiring parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated. CLINIMIX E may be used to treat negative nitrogen balance in patients. There are no adequate or well-controlled studies in pregnant women with CLINIMIX E. Additionally, animal reproduction studies have not been conducted with amino acids and electrolytes and dextrose. It is not known whether CLINIMIX E can cause fetal harm when administered to a pregnant woman. The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. However, the estimated background risk in the U.S. general population of major birth defects is 2 to 4% and of miscarriage is 15 to 20% of clinically recognized pregnancies. Disease-Associated Maternal and/or Embryo-Fetal Risk Based on clinical practice guidelines, parenteral nutrition should be considered in cases of severe maternal malnutriti
CLINIMIX E (amino acids with electrolytes in dextrose with calcium) injection (sulfite-free) is available in 1000 mL and 2000 mL volumes (See Table 9 ). Minimize exposure of CLINIMIX E to heat and avoid excessive heat. Protect from freezing. Store CLINIMIX E at room temperature (25°C/77°F) (may briefly store at up to 40°C/104°F). Refrigerated storage is limited to 9 days once the protective overwrap has been opened. Do not use if the protective overwrap has been previously opened or damaged. For storage of admixed solutions see Dosage and Administration (2.3, 2.4) .
New Drug Application
CLINIMIX E- LEUCINE, PHENYLALANINE, LYSINE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, SERINE, TYROSINE, SODIUM ACETATE, DIBASIC POTASSIUM PHOSPHATE, MAGNESIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, DEXTROSE INJECTION BAXTER HEALTHCARE CORPORATION ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE CLINIMIX E SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR CLINIMIX E. CLINIMIX E (AMINO ACIDS WITH ELECTROLYTES IN DEXTROSE WITH CALCIUM) INJECTION, FOR INTRAVENOUS USE INITIAL U.S. APPROVAL: 1997 RECENT MAJOR CHANGES INDICATIONS AND USAGE CLINIMIX E is indicated as a source of calories, protein, and electrolytes for patients requiring parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated. CLINIMIX E may be used to treat negative nitrogen balance in patients. (1) DOSAGE AND ADMINISTRATION See full prescribing information for information on preparation, administration, instructions for use, dosing considerations, including the recommended dosage in adults and pediatrics, and dosage modifications in patients with kidney disease. (2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8) DOSAGE FORMS AND STRENGTHS CLINIMIX E injection is available in multiple strengths. See full prescribing information for detailed description of each formulation. (3, 11) CONTRAINDICATIONS • • • • WARNINGS AND PRECAUTIONS • • • • • • • • • ADVERSE REACTIONS TO REPORT SUSPECTED ADVERSE REACTIONS, CONTACT BAXTER HEALTHCARE CORPORATION AT 1- 866-888-2472 OR FDA AT 1-800-FDA-1088 OR WWW.FDA.GOV/MEDWATCH USE IN SPECIFIC POPULATIONS SEE 17 FOR PATIENT COUNSELING INFORMATION. REVISED: 4/2021 FULL PRESCRIBING INFORMATION: CONTENTS* 1 INDICATIONS AND USAGE 2 DOSAGE AND ADMINISTRATION 2.1 Preparation Prior to Administration 2.2 Important Administration Instructions 2.3 Instructions for Use 2.4 Preparation and Addition of Lipid Emulsion 2.5 Dosing Consid Soma hati kamili