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Buprenorphine
Opioid (partial µ agonist). No registration in force in Georgia. Forms: solution.
Doses
Each dose comes with its source. Check the label of the product you use.
| Dose | Species | Indication | Route | Frequency | Source |
|---|---|---|---|---|---|
| 10–20 mcg/kg | Dog |
Postoperative Pain Analgesia |
Intravenous / Intramuscular | every 3–4 hours at 10 micrograms/kg or every 5–6 hours at 20 micrograms/kg |
VMD SPC 2025
Official product label (SPC), VMD, UK Approved by the UK Veterinary Medicines Directorate (VMD) as part of the product's authorisation. It applies to that product as authorised there. UK Veterinary Medicines Directorate, 2025 VMD SPC 2025
Official product label (SPC), VMD, UK Approved by the UK Veterinary Medicines Directorate (VMD) as part of the product's authorisation. It applies to that product as authorised there. UK Veterinary Medicines Directorate, 2025 |
| 10–20 mcg/kg | Dog | Sedation | Intramuscular | once, as premedication |
VMD SPC 2025
Official product label (SPC), VMD, UK Approved by the UK Veterinary Medicines Directorate (VMD) as part of the product's authorisation. It applies to that product as authorised there. UK Veterinary Medicines Directorate, 2025 |
| 10–20 mcg/kg | Cat |
Postoperative Pain Analgesia |
Intravenous | as needed; repeat once after 1–2 hours |
VMD SPC 2025
Official product label (SPC), VMD, UK Approved by the UK Veterinary Medicines Directorate (VMD) as part of the product's authorisation. It applies to that product as authorised there. UK Veterinary Medicines Directorate, 2025 |
| 10–20 mcg/kg | Cat |
Postoperative Pain Analgesia |
Intramuscular | as needed; repeat once after 2 hours |
VMD SPC 2025
Official product label (SPC), VMD, UK Approved by the UK Veterinary Medicines Directorate (VMD) as part of the product's authorisation. It applies to that product as authorised there. UK Veterinary Medicines Directorate, 2025 |
Safety information
Known Contraindications
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Critical
Known hypersensitivity to buprenorphine or any excipient is a contraindication.
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Warning
Do not use buprenorphine before caesarean section because it can cause respiratory depression in the offspring around birth. Use cautiously during pregnancy and, if needed after surgery, monitor the dam and neonates closely.
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Warning
Buprenorphine is not recommended during lactation because concentrations in milk can equal or exceed plasma concentrations.
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Warning
Buprenorphine can cause respiratory depression. Use cautiously in animals with impaired respiratory function or in those receiving other drugs that depress respiration.
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Warning
Use buprenorphine cautiously in hepatic impairment, especially biliary-tract disease, because hepatic metabolism affects the intensity and duration of its action.
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Warning
Buprenorphine carries greater risk in renal, cardiac, or hepatic dysfunction and in shock. Use only after a careful benefit-risk assessment with appropriate monitoring.
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Warning
Use buprenorphine cautiously in cardiac dysfunction or shock because cardiovascular adverse effects, including bradycardia and occasionally hypertension or tachycardia, may occur.
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Caution
Do not administer buprenorphine intrathecally or epidurally. Opioid antagonists may not fully reverse its effects; naloxone can help with respiratory depression but repeated dosing or infusion may be required because buprenorphine is long acting.
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Caution
Safety of buprenorphine has not been established in animals younger than 7 weeks.
Known Drug Interactions
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Major warning
Methadone + Buprenorphine
Do not combine buprenorphine with morphine or other opioid analgesics, including fentanyl, pethidine, methadone, or butorphanol, because their analgesic effects may be unpredictable or antagonistic.Recommendation: Do not administer concurrently; buprenorphine may antagonize a mu-opioid agonist.
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Minor warning
Buprenorphine + Acepromazine
Centrally acting drugs, including tranquillisers, sedatives, and hypnotics, can increase buprenorphine-induced drowsiness. Combined use with sedatives can also increase depression of heart rate and respiration.Recommendation: Reduce the sedative dose during premedication; monitor heart rate and respiration.
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Minor warning
Buprenorphine + Dexmedetomidine
Centrally acting drugs, including tranquillisers, sedatives, and hypnotics, can increase buprenorphine-induced drowsiness. Combined use with sedatives can also increase depression of heart rate and respiration.Recommendation: Reduce the sedative dose during premedication; monitor heart rate and respiration.
All forms and registration1
Registration in Georgia and abroad: the register, number, validity and source are behind (i).
Professional reference for veterinary professionals. Not advertising and not a substitute for the product label/SPC.
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This reference is still growing. Missing a product? Let us know. · Report an error or request an addition · Updated: 23 Oct 2026