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POM-V Prescription Required Companion Animal

Vetergesic 0.3 mg/ml Solution for Injection for Dogs and Cats

Active ingredient: Buprenorphine

Form

Injection

Species

Cats Dogs

Manufacturer

Ceva Sante Animale

VMD MA No.

14966/3027

What it's used for

Post-operative analgesia and sedation in the dog. Post-operative analgesia in the cat.

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

The prescription itself has a price. See what practices near you charge for a consultation and the written prescription fee.

Paying less for Buprenorphine

  1. 1

    Ask your vet for a written prescription

    They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.

  2. 2

    Fill it at a registered online retailer

    The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.

Prescription required

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

Clinical information

Vetergesic 0.3 mg/ml Solution for Injection for Dogs and Cats — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.

Post-operative analgesia and sedation in the dog. Post-operative analgesia in
the cat.
Vetergesic should be injected intramuscularly.
SpeciesPost-Operative AnalgesiaSedation
Dog
10 – 20 microgram per kg
(0.3 – 0.6mL per 10kg)
repeated if necessary after
3 – 4 hours with 10
microgram or 5 – 6 hours
with 20 microgram doses.
10 – 20 microgram per kg
(0.3 – 0.6mL per 10kg).
Cat
10 – 20 microgram per kg
(0.3 – 0.6mL per 10kg),
repeated if necessary,
once, after 2 hours.
To ensure that analgesia is present immediately on recovery, the product can
be administered preoperatively. If additional analgesia is subsequently
required, this may be achieved by administration of a further dose of Vetergesic
or concomitant use of a suitable injectable NSAID.
An appropriately graduated syringe must be used to allow accurate dosing.
When administered pre-operatively in conjunction with other premedicants, it
may be possible to reduce the amount of premedicant, such as acepromazine
or medetomidine, and also the amount of inhalational anaesthetic used.

Revised: September 2025
AN: 01877/2025
None known.
Salivation, bradycardia, hypothermia, agitation, dehydration and meiosis can
occur in the dog, and rarely hypertension and tachycardia.
Mydriasis and signs of euphoria (excessive purring, pacing, rubbing) commonly
occur in cats and will usually resolve within 24 hours.
Animals administered opioids possessing sedative and analgesic properties
may show variable responses. Therefore, the responses of individual animals
should be monitored and subsequent doses should be adjusted accordingly. In
some cases repeat doses may fail to provide additional analgesia. In these
cases, consideration should be given to use of an analgesic from an alternative
class.

the person administering the medicinal product to the animal
i) Special Precautions for use in animals
Buprenorphine may occasionally cause significant respiratory depression
and, as with other opioid drugs, care should be taken when treating

Revised: September 2025
AN: 01877/2025
animals with impaired respiratory function or animals that are receiving
drugs that can cause respiratory depression. Volunteer studies in man
have indicated that opiate antagonists may not fully reverse the effects of
buprenorphine. Naloxone may be of benefit in reversing reduced
respiratory rate and respiratory stimulants such as Doxapram are also
effective in man. Because of the prolonged duration of effect of
buprenorphine in comparison to such drugs, they may need to be
administered repeatedly or by continuous infusion.
Buprenorphine may cause some drowsiness, which may be potentiated by
other centrally-acting agents, including tranquillisers, sedatives and
hypnotics. The product should not be used in conjunction with morphine
or other opioid-type analgesics (e.g. etorphine, fentanyl, pethidine,
methadone, papaveretum and butorphanol).
As buprenorphine is metabolised by the liver, its intensity and duration of
action may be affected in animals with impaired liver function.
Safety has not been fully evaluated in clinically compromised cats e.g.
those suffering from renal or hepatic dysfunction, cardiovascular disease
or shock. Use in such cases should be based on the risk-benefit
assessment of the veterinarian.
Repeated administration earlier than the recommended repeat interval
suggested in Section 4.9 is not recommended.
ii) Special precautions to be taken by the person administering the medicinal
product to the animals.
Wash hands/affected area thoroughly after any accidental spillage
Care should be taken to avoid accidental self-injection.
Following accidental self-injection or ingestion, seek medical advice taking
the product literature with you.
Following eye contamination or skin contact, wash thoroughly with cold
running water. Seek medical advice if irritation persists.
Buprenorphine may cause some drowsiness, which may be potentiated by
other centrally acting agents, including tranquillisers, sedatives and hypnotics.
Although there is evidence in humans to indicate that therapeutic doses of
buprenorphine do not reduce the analgesic efficacy of standard doses of an
opioid agonist and that when buprenorphine is employed within the normal
therapeutic range, standard doses of opioid agonist may be administered before
the effects of the former have ended without compromising analgesia, it is
recommended that buprenorphine is not used in conjunction with morphine or
other opioid-type analgesics, e.g. etorphine, fentanyl, pethidine, methadone,
papaveretum or butorphanol.
Vetergesic has been used successfully with a wide range of premedicant and
anaesthetic agents including acepromazine, alphaxalone/alphadalone, atropine,
halothane, isoflurane, ketamine, medetomidine, propofol, sevoflurane,
thiopentone and xylazine without any observed adverse effects.
This veterinary medicinal product does not require any special temperature
storage conditions.
Protect from light.
This product does not contain an antimicrobial preservative. Any solution
remaining in an ampoule following withdrawal of the required dose should be
discarded.
Not applicable.
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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