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POM-V Prescription Required Companion Animal

Hypertonic 72 mg/ml Solution for Infusion for Cattle, Cattle (Calves), Horses, Dogs and Cats

Active ingredient: Sodium Chloride

Form

Solution

Species

Cats Cattle Dogs Horses

Manufacturer

Dechra Regulatory B.V.

VMD MA No.

50406/5038

What it's used for

As an oral rehydration therapy for the treatment of diarrhoea in calves by reversing the process of dehydration, acidosis and loss of electrolytes associat...

Full indications, dosage and side effects ↓
View official SPC (PDF)

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Paying less for Sodium Chloride

  1. 1

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  2. 2

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Prescription required

Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.

Clinical information

Hypertonic 72 mg/ml Solution for Infusion for Cattle, Cattle (Calves), Horses, Dogs and Cats — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

As an oral rehydration therapy for the treatment of diarrhoea in calves by reversing the
process of dehydration, acidosis and loss of electrolytes associated with diarrhoea,
whether caused by bacteria, viruses, cryptosporidia or inappropriate nutrition.
The infusion should ideally be warmed to approximately 37 °C prior to administration.
Recommended doses are in the range 4 -8 ml/kg, and an infusion rate of
1 ml/kg/minute should not be exceeded.
The veterinary medicinal product should be used in conjunction with conventional
fluid therapy. The administration of the veterinary medicinal product is usually
followed by the intravenous administration of an isotonic intravenous fluid (e.g. an
intravenous 0.9 % sodium chloride solution).
Fluid output, plasma sodium concentration and blood pressure should be monitored.
Adequate access to drinking water should also be provided.
Strict observation of the patient is necessary to safeguard the maintenance of correct
diuresis.
Do not use in animals with:




AN: 02591/2024, 02593/2024, 03220/2024, 03566/2024, 04026/2024 and 04027/2024




Cattle, cattle (calves), horses, dogs and cats:
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Death
a
Undetermined frequency
(cannot be estimated from the
available data)
Hypokalaemia
b
, Haemolysis
c
, Haemoglobinuria
c
Oedema
c, d
Hypotension
c
, Arrhythmia
c
Pulmonary oedema
c,d
, Respiratory tract
disorder
c,e
, Hyperventilation
c
Polyuria
f

Thrombosis
Injection site pain
g
a
Due to erroneous administration of sodium to dehydrated animals which may
increase the existing extracellular hypertonia, with aggravation of existing disorders.
b
May be induced by an excess of sodium and may be aggravated by the existence of
continued loss of potassium and hyperchloraemia.
c
After rapid administration.
d
Especially in cases of concurrent cardiac or renal insufficiency.
e
Bronchoconstriction.
f
With formation of hypertonic urine.
g
Administration into small peripheral veins may cause signs of pain.
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to
either the marketing authorisation holder or its local representative or the national
competent authority via the national reporting system. See the package leaflet for
respective contact details.
AN: 02591/2024, 02593/2024, 03220/2024, 03566/2024, 04026/2024 and 04027/2024
None.

Special precautions for safe use in the target species:
Do not use unless the solution is clear, free from visible particles, and the container is
undamaged.
Maintain aseptic precautions.
Administration of the solution must be accompanied by an opportunity for the animal
to drink ad libitum.
This veterinary medicinal product should ideally be warmed to approximately 37 °C
prior to the administration of large volumes, or if the administration rate is high, in
order to avoid hypothermia.
Any existing haemorrhage should be stopped or controlled before treatment.
Hypertonic solutions must be administered solely by the intravenous route.
Animals treated with this veterinary medicinal product should be closely observed for
possible deterioration of the clinical condition as a consequence of treatment.
Repeated infusion should only be performed after checking sodium concentration
and acid-base status.
Rapid infusion of hypertonic NaCl can lead to myelinolysis in the brain in animals with
chronic hyponatraemia.
Do not use the veterinary medicinal product as a vehicle for the administration of
other veterinary medicinal products.
Care should be taken to avoid the use of excessive doses (>8 ml/kg) and excessive
dose rates (>1 ml/kg/minute).
Excessive administration of chloride may, due to the electrolytes’ interaction with the
body’s bicarbonate buffer system exert an acidifying effect. Therefore, in clinical
AN: 02591/2024, 02593/2024, 03220/2024, 03566/2024, 04026/2024 and 04027/2024
instances accompanied by acidosis and hyperchloremia, special care has to be taken
if this veterinary medicinal product is to be infused.
Sodium chloride administration may aggravate a pre-existing hypokalaemia.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
None.
Special precautions for the protection of the environment:
Not applicable.
Administer with care to animals that have had prolonged treatment with
corticosteroids having a mineralocorticoid action.
Do not store above 25 °C.
Do not freeze.
Meat and offal: Zero days;
Milk: Zero hours.
4.

This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.

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