Vetofol 1.0% w/v Emulsion for Injection
Active ingredient: Propofol
Form
Injection
Species
Manufacturer
Norbrook Laboratories Limited
VMD MA No.
02000/4244
What it's used for
Vetofol Injection is indicated for use in dogs and cats as a short-acting, intravenous general anaesthetic for procedures of short duration, lasting up to...
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Vetofol 1.0% w/v Emulsion for Injection — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
general anaesthetic for procedures of short duration, lasting up to 5 minutes; for the
induction and maintenance of general anaesthesia using incremental doses to
effect; for the induction of general anaesthesia where maintenance is provided by
inhalation anaesthetics. The product is particularly suitable for cases where a short
recovery period is desired.
should be shaken thoroughly before opening.
Induction: The induction dose is calculated according to bodyweight and may be
administered to effect over a period of 10 to 40 seconds. Alternatively, the
calculated dose may be given in full as a single bolus. The induction dose is
reduced by the use of premedicants.
The following dose rates are for guidance and in practice the dose rate should be
based on response.
The average induction dose for dogs and cats, either unpremedicated or when
premedicated with a tranquilliser such as acepromazine, is as follows:
Dose rate (mg/kg
bodyweight)
Dose volume (ml/kg
bodyweight)
DogsUnpremedicated6.56.5 ml/10 kgPremedicated4.04.0 ml/10 kgCatsUnpremedicated8.02.0 ml/2.5 kgPremedicated6.01.5 ml/2.5 kg
Maintenance: Where anaesthesia is maintained by incremental injections, the dose
rate will vary between animals. Incremental doses should be given to effect. Doses
of around 1 ml per 4.0 – 8.0 kg bodyweight sustain anaesthesia for periods of up to
5 minutes.
Maintenance by inhalation agents: Where inhalation agents are used to maintain
general anaesthesia, clinical experience indicates that there may be a need to use
a higher initial concentration of inhalation agent than is normally the case following
induction with barbiturate agents such as thiopentone.
is generally smooth, minimal evidence of excitation has been observed in a small
proportion of animals.
In clinical trials in cats, transient apnoea during induction and paw/face licking
characteristics during recovery have been observed in a small proportion of
animals.
If panting is evident before induction, it may continue throughout the subsequent
periods of anaesthesia and recovery.
Revised: March 2011
AN: 01228/2009
Special precautions for use in animals
Shake the vial gently but thoroughly before opening. Do not use if evidence of
phase separation remains after gentle shaking.
During induction of anaesthesia, mild hypotension and transient apnoea, similar to
effects with other intravenous anaesthetic agents may occur.
When using the product, facilities for the maintenance of a patent airway, artificial
ventilation and oxygen enrichment should be available.
Inadvertent perivascular administration rarely causes local tissue reactions.
As with other intravenous anaesthetic agents, caution should be exercised in dogs
and cats with cardiac, respiratory, renal or hepatic impairment, or in hypovolaemic
or debilitated animals.
If the product is injected very slowly, an inadequate plane of anaesthesia can occur.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals
This is a potent drug: particular care should be taken to avoid accidental self-
administration. Preferably use a guarded needle until the moment of injection.
Wash off splashes from the skin and eyes immediately.
In the event of accidental self- administration, seek urgent medical attention and
show the label.
Advice to doctor: Do not leave the patient unattended. Maintain airways and give
symptomatic and supportive treatment.
atropine, acepromazine, diazepam; inhalational agents e.g. halothane, nitrous
oxide, enflurane and analgesic agents e.g. pethidine, buprenorphine. No
pharmacological incompatibility has been encountered.
Do not freeze.
Protect from light.
Withdrawn product should be used immediately. Product remaining in the container
should be discarded.
Avoid the introduction of contamination.
Revised: March 2011
AN: 01228/2009
Revised: March 2011
AN: 01228/2009
5.
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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Other Products Containing Propofol
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Inductofol 10 mg/ml Emulsion for Injection for Cats and Dogs
POM-VNorbrook Laboratories Limited
Norofol 10 mg/ml Emulsion for Injection for Cats and Dogs
POM-VNorbrook Laboratories Limited
Propodine 10 mg/ml Emulsion for Injection / Infusion for Dogs and Cats
POM-VDechra Regulatory BV
PropoFlo Plus, 10 mg/ml, Emulsion for Injection for Dogs and Cats
POM-VZoetis Belgium S.A.
PropoFlo Plus, 10 mg/ml, Emulsion for Injection for Dogs and Cats
POM-VZoetis UK Limited
Propofol-Lipuro Vet 10 mg/ml Emulsion for Injection
POM-VB. Braun Melsungen AG
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