Veterinary: Torbutrol, Torbugesic
- Torbutrol tablets: 1 mg, 5 mg, 10 mg
- Suspension: variety of strengths can be obtained from compounding pharmacies, online, through prescription from veterinarian (e.g., Wedgewood Pharmacy, based in New Jersey: https://www.wedgewoodpharmacy.com/items/pimobendan-oral-suspension.html).
- Torbutrol injectable: 0.5 mg/mL in 10 mL vials
- Torbugesic injectable: 10 mg/mL in 50 mL vials
- Stadol injectable: 1 mg/mL, 2 mg/mL
Butorphanol is a synthetic partial opiate agonist that is structurally related to Morphine. It is a more potent analgesic than Morphine, but unlike Morphine it possess less cardiovascular effects, and respiratory center sensitivity.
It’s actions are similar to that of other partial agonists such as, pentazocine or nalbuphine. The agonist activity of butorphanol is believed to be exerted at the kappa and sigma receptors.
Butorphanol binds to opiate receptors at sites in the central nervous system and alters perception and response to pain. It also has the ability to act as an antitussive.
Duration of action following dose appears to be 4 hours.
It is absorbed in the gut with its highest distribution levels being in the kidney, liver, and intestine. Levels throughout other tissues are found to be higher than plasma. The drug is metabolized in the liver, crosses placental barrier, and distributed into breast milk. It is excreted in urine and bile, and eliminated in the feces.
Safety in pregnant and very young animals has not been determined.
Used as an analgesic and a sedative.
Drug Interactions or Contraindications
- Incompatible mixed with dimenhydrinate and pentobaritol sodium.
- Use cautiously in hypothyroidism, severe renal insufficiency, or severely debilitated.
- Butorphanol, if used with other central nervous system depressants may increase the CNS or respiratory depression of those drugs. It is recommended to decrease butorphanol’s dosage if used in conjunction with those particular drugs.
CNS: sedation, confusion, lethargy, agitation.
Resp: decreased respiratory rate
GU: urinary retention
In the event there are signs of overdose such as cardiac and respiratory depression administer the following:
0.5 mg/kg to 2 mg/kg , SQ , q6hr 2
0.2 mg/kg to 2 mg/kg , q2hr to q4hr 35, 41
1 mg/kg to 5 mg/kg , SQ , q2hr to q4hr 1 (Sedation)
1 mg/kg to 5 mg/kg , SQ , q4hr 42 (Sedation), 41
0.18 mg/lb to 10 mg/lb SQ , or 1 mg/lb , PO , q4hr to q6hr 3, 12
0.25 mg/lb to 1 mg/lb , SQ (effective for pain) 3, 12
When combined with diazepam: 0.25 mg/lb butorphanol and 1 mg/lb diazepam. 3, 12
- Note to veterinarians: the chance of rats developing pica following the use of butorphanol may be less than it is with buprenorphine due to butorphanol’s short duration of action.
However, it is advised to instruct pet owners to monitor for this behavior if an opioid medication is given, and to contact vet immediately. Also have the pet owner remove the rat from any bedding source that might be chewed and ingested until medication has passed through the system.
It is also important to be aware that pica may be observed, in rats, where pain has not been adequately addressed.
- Store drug at room temperature away from light.
- Anesthesia and Analgesia in Laboratory Animals at UCSF. (2018, April ). Retrieved September 5, 2020, from https://larc.ucsf.edu/veterinary-information.
- Takeda, N., Hasegawa, S., Morita, M., & Matsunaga, T. (1993). Pica in rats is analogous to emesis: an animal model in emesis research. Pharmacology, biochemistry, and behavior, 45(4), 817–821. https://doi.org/10.1016/0091-3057(93)90126-e