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OsmoSol-R 7.4

This page contains information on OsmoSol-R 7.4 for veterinary use.
The information provided typically includes the following:
  • OsmoSol-R 7.4 Indications
  • Warnings and cautions for OsmoSol-R 7.4
  • Direction and dosage information for OsmoSol-R 7.4

OsmoSol-R 7.4

This treatment applies to the following species:
Company: VetOne

Multiple Electrolytes Injection Type, 1 USP

STERILE NONPYROGENIC SOLUTION

For Animal Use Only

Description

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) is a sterile, non-pyrogenic isotonic solution intended for fluid and electrolyte replenishment in single dose containers. May be administered intravenously using aseptic technique. It contains no antimicrobial agents. Discard any unused portion. The pH is adjusted with Sodium Hydroxide. Composition, osmolarity, pH and ionic concentration and caloric content are shown in Table 1.

Table 1

Composition (g/L)

Sodium Chloride

5.26

Sodium Gluconate

5.02

Sodium Acetate Trihydrate

3.68

Potassium Chloride

0.37

Magnesium Chloride

0.30

Ionic Concentration (mEq/L)

Sodium

140

Potassium

5

Magnesium

3

Chloride

98

Acetate

27

Gluconate

23

Osmolarity (mOsmol/L) (calc): 294 mOsmol per litre

pH: 7.4 (limit 6.5 to 8.0)

Caloric Content (kcal/L): 21

The container is free of PVC and phthalates. The container meets the requirements of USP and is registered with US FDA.

Clinical Pharmacology

A multiple electrolyte intravenous solution is intended to restore the electrolyte balance and water for hydration. It is capable of inducing diuresis depending on the clinical condition of the patient and produces a metabolic alkalinizing effect. Acetate and gluconate ions are metabolized ultimately to carbon dioxide and water, which requires the consumption of hydrogen cations.

OsmoSol-R 7.4 Indications

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) is indicated as a source of water and electrolytes for all species. It is also used as an alkalinizing agent.

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, 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 priming solution), added to or infused concurrently with blood components, or used as a diluent in the transfusion of packed erythrocytes.

Contraindications

None known

Warnings

The introduction of additives to any solution, regardless of type of container, requires special attention to ensure that no incompatibilities result. While some incompatibilities are readily absorbed, one must be aware that subtle physical, chemical and pharmacological incompatibilities can occur. The medical literature, the package insert and other available sources of information should be reviewed for thorough understanding of possible incompatibilities.

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema and sodium retention.

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) should be used with great care, if at all, in patients with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) should be used with great care in patients with metabolic or respiratory alkalosis. The administration of acetate or gluconate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.

The intravenous administration of VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, over-hydration, congested states, or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentrations of the injection. The risk of solute overloading causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections.

In patients with diminished renal function, administration of VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) may result in sodium or potassium retention.

Adverse Reactions

Adverse reactions may occur due to the solution or the technique of administration including febrile response, infection at the site of injection or allergic reactions. Prolonged intravenous infusion of this type of product may cause venous thrombosis or phlebitis extending from the site of injection, extravasation, and hypervolemia.

If an adverse reaction does occur, discontinue the infusion and evaluate the patient, institute appropriate therapeutic countermeasures, and save the remainder of the fluid for examination if deemed necessary.

Precautions

This is a single dose unit. It contains no preservatives. Use entire contents when first opened.

Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations, and acid base balance during prolonged therapy or whenever the condition of the patient warrants such evaluation.

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) should be used with caution. Excess administration may result in metabolic alkalosis.

Caution must be exercised in the administration of VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) to patients receiving corticosteroids or corticotropin.

Do not administer unless solution is clear and both seal and container are intact.

Solution must be warmed to body temperature prior to administration and administered at a slow rate. Use solution promptly following initial entry.

Reactions which may occur because of the solution or the technique of administration, include febrile response, infection at the site of injection, extravasation, and hypervolemia.

If an adverse reaction does occur, discontinue the infusion and evaluate the patient, institute appropriate therapeutic countermeasures, and save the remainder of the fluid for examination if deemed necessary.

Dosage and Administration

To be used as directed by a licensed veterinarian. The dosage of the VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) is dependent upon the age, weight and clinical conditions of the patient as well as laboratory determinations. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration.

For use in one patient on one occasion only. Discard any unused portion. Care should be taken with administration technique to avoid administration site reactions and infection.

Additives may be incompatible. Complete information is not available. Those additives known to be incompatible should not be used. Consult with Pharmacist, if available. If, in the informed judgement 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.

Over-dosage

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

Packs Supplied

VetOne OsmoSol-R 7.4 (Multiple Electrolyte Injection, Type 1, USP) in plastic container is available as follows:

Size (mL)

Item Code

NDC

1000

501205

13985-932-01

5000

501206

13985-932-05

Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. It is recommended the product be stored at room temperature (86°F/30°C). Protect from freezing.

Storage

Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. It is recommended the product be stored at room temperature (86°F/30°C). Protect from freezing.

Directions for use of plastic container

To Open

Tear overwrap 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 solution container firmly. If leaks are found, discard solution as sterility may be impaired. If supplemental medication is desired, follow directions below:

Preparation for Administration

1. Suspend container from eyelet support.

2. Remove plastic protector from inlet/outlet port at bottom of container.

3. Attach administration set.

To Add Medication

WARNING: Additives may be incompatible.

To add medication before solution administration

1. Prepare medication site.

2. Using syringe with 0.63mm to 0.80mm needle, puncture medication port and inject.

3. Mix solution and medication thoroughly. For high density medication such as potassium chloride, squeeze ports while ports are upright and mix thoroughly.

To add medication during solution administration

1. Close the clamp on the administration set.

2. Prepare medication site.

3. Using syringe with 0.63mm to 0.80mm needle, puncture medication port and inject.

4. Remove container from IV pole and/or turn to an upright position.

5. Evacuate both ports by squeezing them while container is in the upright position.

6. Mix solution and medication thoroughly.

7. Return container to in use position and continue administration.

KEEP OUT OF REACH OF CHILDREN.

OsmoSol-R 7.4 Caution

FEDERAL LAW RESTRICTS THIS DRUG TO USE BY OR ON THE ORDER OF A LICENSED VETERINARIAN.

Made in Australia

Manufactured by: Sypharma Pty Ltd, 27 Healey Road Dandenong, Victoria 3175 Australia

Distributed by: MWI, Boise, ID 83705

www.VetOne.net

Iss. 04/18

1000 mL (33.81 fl. oz.)

Iss. 08/18

5000 mL (169.07 fl. oz.)

Iss. 08/18

CPN: 1315264.0

VET ONE
Distributed by MWI Animal Health

3041 W. PASADENA DR., BOISE, ID, 83705
Customer Service:   888-694-8381
Toll-Free:   800-824-3703
Website:   www.mwianimalhealth.com
    www.vetone.net
Every effort has been made to ensure the accuracy of the OsmoSol-R 7.4 information published above. However, it remains the responsibility of the readers to familiarize themselves with the product information contained on the US product label or package insert.

Copyright © 2019 Animalytix LLC. Updated: 2019-09-30

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