Land: USA
Språk: engelska
Källa: NLM (National Library of Medicine)
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37), SODIUM GLUCONATE (UNII: R6Q3791S76) (GLUCONIC ACID - UNII:R4R8J0Q44B, SODIUM CATION - UNII:LYR4M0NH37), SODIUM ACETATE (UNII: 4550K0SC9B) (ACETATE ION - UNII:569DQM74SC, SODIUM CATION - UNII:LYR4M0NH37), POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698), MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838, CHLORIDE ION - UNI
Vedco, Inc.
SODIUM CHLORIDE
SODIUM CHLORIDE 526 mg in 100 mL
INTRAVENOUS
PRESCRIPTION
Veterinary VEDALYTE 7.4 Injection, USP is indicated as a source of water and electrolytes or as an alkalinizing agent Veterinary VEDALYTE 7.4 Injection, USP is compatible with blood or blood components. it may be administered prior to or following the infusion of blood through the same administration set (i.e. as a primary solution), added to or infused concurrently with blood components or used a diluent in the transfusion of packed erythrocytes. VEDALYTE 7.4 Injection, USP and 0.9% Sodium Chloride Injection, USP are equally compatible with blood or blood components None Known To Open Tear overwrap down side at slit and remove solution container. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually. Check for minute leaks by squeezing inner bag firmly. If leaks are found, discard solution as sterility may be impaired. If supplemental medicat
Veterinary VEDALYTE 7.4 Injection, USP in plastic container is available as follows: Plastic Container: *PVC Free, DEHP Free, Latex Free Bag. ** The plastic container is fabricated from a specially formulated polyvinyl chloride. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di-2-ethylhexyl phthalate (DEHP), upto 5 parts per million. However safety of the plastic has been confirmed in animals according to USP biological tests for plastic containers, as well as tissue culture toxicity studies.
unapproved drug other
VETERINARY VEDALYTE - SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE TRIHYDRATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE INJECTION VEDCO, INC. _Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been_ _approved by FDA. For further information about unapproved drugs, click here._ ---------- VETERINARY VEDALYTE 7.4 INJECTION, USP For Animal Use Only DES CRIPTION Veterinary VEDALYTE 7.4 Injection, USP is a sterile, nonpyrogenic isotonic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. It contains no antimicrobial agents or preservatives. Discard unused portion. The pH is adjusted with sodium hydroxide. Composition, osmolarity, pH, ionic concentration and caloric content are shown in Table 1: CLINICAL PHARMACOLOGY Veterinary VEDALYTE 7.4 Injection, USP administered intravenously has a value as a source of water, electrolytes and calories. Normal physiological osmolarity range is 280 to 310 mOsmol/L. Administration of substantially hypertonic solutions may cause vein damage. It is capable of inducing diuresis, depending on the clinical condition of the patient. Veterinary VEDALYTE 7.4 Injection, USP produces a metabolic alkalinilizing effect. Acetate and gluconate ions are metabolized ultimately to carbon dioxide and water, which requires consumption of hydrogen cations INDICATIONS AND USAGE Veterinary VEDALYTE 7.4 Injection, USP is indicated as a source of water and electrolytes or as an alkalinizing agent Veterinary VEDALYTE 7.4 Injection, USP is compatible with blood or blood components. it may be administered prior to or following the infusion of blood through the same administration set (i.e. as a primary solution), added to or infused concurrently with blood components or used a diluent in the transfusion of packed erythrocytes. VEDALYTE 7.4 Injection, USP and 0.9% Sodium Chloride Injection, USP are equally compatible with blood or blood components CONTRAINDICATIONS None Known WARNINGS Veterinary VEDALYTE Läs hela dokumentet