Animal NDC 72483-201-25 Alfa Veterinary 10% Dextrose

10% Dextrose

Alfa Veterinary 10% Dextrose Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Description

DESCRIPTION:10% dextrose solution is sterile, non-pyrogenic for fluid and calorie replacement, and is supplied in single-dose containers for intravenous administration. Discard the unused portion. Does not contain antimicrobial agents.Chemically, dextrose (glucose) is a monosaccaride containing an aldehyde group (an aldose). In water it exists primarily as a six membered hemi-acetal ring in equilibrium with a minor amount of the free aldehyde form and a five membered hemicetal form. Dextrose used is either an anhydrous or monohydrate form.The Plastic container, a semi-rigid bottle, is made of a low-denisty polyethylene which is a flexible and resistant material. No venting is necessary during infusion.COMPOSITION:Each 100ml containsDextrose monohydrate 11.0g equivalent 10g dextrose; Water for injection q.s.Total osmolarity Calc is 556 milliomoles per literP.H. 3.2-6.5​

Clinical Pharmacology

10% Dextrose solution has value as a source of water and calories. It is capable of inducing diuresis depending on the clinical condition of the partient. Glucose is a nutrient of the first order, provides 4.1Kcal per gram and like all carbohydrates has the property of decreasing catabolism.

Veterinary Indications

INDICATIONS AND USAGE:10% dextrose dolution has value as a source of water and calories. It is used to decrease the excessive pressure of spinal brain fluid, also a scloerisng to treat varicose veins and decrease intracranial pressure.

Warnings

WARNING:10% Dextrose Injection should not be administered simultaneously with blood through the same administration set because of the possibility of pseudoagglutination or hemolysis. The intravenous administration of 10% Dextrose Injection can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, over hydration, congested states, or pulmonary edema. The risk of dilutive states is inversely proportional to the electrolyte concentrations of the injections.The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections. Excessive administration of dextrose injections may result in significant hypokalemia.

Adverse Reactions

ADVERSE REACTIONS:Reactions which may occur because of the injection or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia.If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.

Precautions

PRECAUTIONS:Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations and acid base balance during prolonged parenteral therapy or whenever the condition of the patient warrants such evaluation. 10% Dextrose Injection should be used with caution in patients with overt or subclinical diabetes mellitus. Do not administer unless solution is clear and seal is intact. This is a hypotonic solution and as such should not be used for resuscitation.

Overdosage

OVERDOSAGE:In an event of over hydration or solute overload, re-evaluate the patient and institute appropriate corrective measures. See Warnings, Precautions, and Adverse Reactions.

Dosage & Administration

DOSAGE AND ADMINISTRATION:As directed by a veterinarian. Dosage is dependent upon the age, weight and clinical condition of the patient as well as laboratory determinations. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. All injections in plastic containers are intended for intravenous administration using sterile equipment. Additives may be incompatible. Complete information is not available. Those additives known to be incompatible should not be used. Consult with veterinarian, if available. If, in the informed judgment of the veterinarian, it is deemed advisable to introduce additives, use aseptic technique. Mix thoroughly when additives have been introduced. Do not store solutions containing additives.

  • DIRECTIONS FOR USE PLASTIC CONTAINER:To OpenCheck for minute leaks by squeezing the container firmly. If leaks are found, discard solution as sterility may be impaired. Use the solution immediately after the bottle is opened, discard the remaining one. Discard unused portion. If supplemental medication is desired follow directions below:Preparation and administrationCheck for minute leaks by squeezing the container firmly. If leaks are found, discard solution as sterility may be impaired.Remove Plastic protector from ports area at the bottom of container.Hold the bottle in vertical position and inset pyrogen free IV administration set in the outlet port. Use aseptic TechniqueSuspend container from eyelet supportTo Add MedicationWARNING: Additives may be incompatible.To add medication before solution administration1. Prepare medication site.2. Using syringe with 19 to 22 gauge needle, puncture inlet port and inject.3. Mix solution and medication thoroughly.To add medication during solution administration1. Close clamp on the set.2. Prepare medication site.3. Using syringe with 19 to 22 gauge needle, puncture inlet port and inject.4. Remove container from IV pole and/or turn to an upright position.5. Mix solution and medication thoroughly.6. Return container to in use position and continue administration.CAUTION: Federal law (USA) restricts this drug to use by or on the order of a licensed veterinarian.

Storage And Handling

STORAGE: Store at temperatures no higher than 30ºC (86ºF). Keep out of the reach of children

Information For Owners/Caregivers

Manfactured by:LABORATORIOS ALFA S.R.L.,Santo Domingo, Dominican RepublicRevised March 2019

* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.