Analgesic properties are based mostly on its selective agonism to the μ-opioid receptor (MOR) which is crucial for transmission of information about pain throughout the central nervous system. These receptors are located mostly in brainstem and thalamus.
Agonism to δ-opioid receptor (DOR) in nucleus accumbens mediates activation of the “reward pathway”.
Indications and dose
Pharmacokinetics
Onset of action:
Oral: 20–40 minutes
IV: 1–2 minutes
Duration of action:
Oral: 3–6 hours
IV: 3–4 hours
Half-life of elimination: 2–3 hours
Metabolism: Hepatic, partly renal glucuronidation
Elimination: Kidneys (90 %), liver (10 %)
Directions for administration
Lowest effective dose for shortest time possible is recommended.
Intravenous injections should be given over 2-3 minutes.
The oral drops should be diluted in water before administration.
he dose should be divided by 3 when patients are transferred from an oral morphine form to an intravenous form, and halved when transferred to a subcutaneous form.