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It is well absorbed IM, and SQ, and is metabolized in the liver.
In rats, the drug concentrates in the liver, brain, gastrointestinal tract and placenta. It is then excreted in urine, and via breast milk.
It’s duration of action may last from 8 to 12 hours.
There is no evidence at this time of teratogenicity.
Compatible drugs are acepromazine, atropine, diphenhydramine, droperidol, glycopyrolate, hydroxyzine, scopolamine, and xylazine.
If used with other central nervous system depressants such as anesthetic agents, Antihistamines, phenothiazines, barbiturates and tranquilizers, may increase central nervous system, and respiratory depression.
Recommended not to use with MAO inhibitors.
Use with caution in respiratory compromise, and impaired liver or renal function.
CV: bradycardia
Respiratory: decreased respiratory rate GI: constipation
GU: urinary retention
Skin: itching
Other: In the event of signs of overdose, such as cardiac and respiratory depression, administer naloxone 0.01 to 0.10 mg/kg SC, IP (narcotic reversal) (1), fluids, O2, and vasopressors.
or
0.05 mg/kg to 0.1 mg/kg , SQ , q6hrs to q12hrs 2
See also Rat Analgesics,
by:Frank J Golder BVSc BPhil
Diplomate American College of Veterinary Anesthesiologists
Department of Physiological Sciences
College of Veterinary Medicine
Posted on June 23, 2003, 14:44,
Last updated on March 17, 2008, 16:18
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