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NERVOUS SYSTEM › ANALGESICS › OPIOIDS › Natural opium alkaloids
morphine, combinations
N02AA51
Forms & Strengths
- Oral capsules, extended-release (morphine/naltrexone combinations)
- Oral tablets, extended-release
- Injectable solutions (morphine sulfate with various adjuvants)
Adult Dosing
- Pain, chronic severe: Titrated individually based on previous analgesic history, opioid tolerance, and patient response.
- Conversion from other opioids: Utilize standard equianalgesic conversion tables, reducing dose by 25-50% to account for incomplete cross-tolerance.
Pediatric Dosing
- Safety and efficacy in pediatric patients not established for combination formulations.
- Use restricted primarily to single-entity morphine formulations under specialist supervision in inpatient settings.
Indications
- Management of chronic, severe pain requiring continuous, around-the-clock opioid analgesia for an extended period.
- Pain unresponsive to lesser analgesic modalities.
Mechanism of Action
- Agonist at mu, kappa, and delta opioid receptors in the central nervous system and periphery, altering pain perception and response.
- Formulations with naltrexone or other antagonists are designed to deter misuse or abuse via the oral or intravenous route while maintaining analgesia.
Contraindications
- Significant respiratory depression
- Acute or severe bronchial asthma in an unmonitored setting or absence of resuscitative equipment
- Known or suspected gastrointestinal obstruction, including paralytic ileus
- Hypersensitivity to morphine or any component of the formulation
Adverse Reactions
- Respiratory depression and arrest
- Central nervous system depression (somnolence, dizziness, sedation)
- Constipation, nausea, vomiting
- Hypotension, orthostatic hypotension
- Physical dependence, tolerance, and opioid use disorder
Drug Interactions
- Central nervous system depressants (alcohol, benzodiazepines, general anesthetics): profound sedation, respiratory depression, coma, and death.
- CYP3A4 and UGT inhibitors/inducers may alter the metabolism of associated agents.
- Serotonergic drugs (SSRIs, SNRIs, MAOIs): increased risk of serotonin syndrome.
- Mixed agonist-antagonist/partial agonist opioid analgesics: may precipitate withdrawal symptoms or reduce analgesic effect.
Curated Content: Needs Vetting Before Put to Clinical Use