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Opioid Analgesic — Strong Pregnancy: Regular use during pregnancy may cause drug dependence in the foetus, leading to withdrawal symptoms in the neonate; if opioid use is required for a prolonged period, advise the patient of the risk of neonatal opioid withdrawal syndrome and ensure appropriate treatment will be available. Administration during labour may depress neonatal respiration and an antidote for the child should be readily available. Breast-feeding: administration to nursing women is not recommended — morphine may be secreted in breast milk and cause infant respiratory depression. Long-term opioid use can cause hypogonadism and adrenal insufficiency in both sexes.

Morphine (Orthopaedic Acute Pain)

Brand names: Oramorph, MST Continus, Sevredol, Morphgesic

Morphine is a strong opioid analgesic used for moderate-to-severe acute orthopaedic pain such as fractures and post-injury pain, given by oral or parenteral routes.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 10–20 mg (5–10 ml of 10 mg/5 ml oral solution)
Route: Oral
Frequency: Every 4 hours
Max: 120 mg per day
ROUTE CAVEAT: the fetched UK SPC is Morphine 10 mg/5 ml Oral Solution, so this source gives ORAL dosing only. It contains NO intravenous, subcutaneous or intramuscular morphine regimen — the parenteral doses commonly used for acute orthopaedic and post-operative pain are not covered by this bundle and must be sourced separately. The SPC notes that when the oral solution is used in place of parenteral morphine, a 50% to 100% increase in dosage is usually required to achieve the same level of analgesia. Dosage can be increased under medical supervision according to the severity of the pain and the patient's previous history of analgesic requirements. Reductions in dosage may be appropriate in the elderly and in patients with chronic hepatic disease, renal impairment, severe hypothyroidism, adrenocortical insufficiency, prostatic hypertrophy, shock, or where sedation is undesirable. Before initiating, agree a treatment strategy including duration, goals and a plan for ending treatment; maintain frequent physician–patient contact; taper gradually when therapy is no longer required to prevent withdrawal. Should not be used longer than necessary. In the absence of adequate pain control, consider hyperalgesia, tolerance and progression of the underlying disease. When transferring from other morphine preparations, dosage titration may be appropriate. PAEDIATRIC: the SPC gives age-banded oral regimens for 13–18 years, 6–12 years and 1–5 years, and states morphine oral solution is not recommended in children under 1 year. Verify any paediatric dose against a children's formulary. Source quote (§4.2): 'Adults: Recommended dose: 10-20 mg (5-10 ml) every 4 hours. Maximum daily dose: 120 mg per day'.

Dose adjustments

Renal

The SPC states only that reductions in dosage may be appropriate in patients with renal impairment (§4.2 special populations); no numeric renal dose adjustment is given.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Known hypersensitivity to the active substance or to any of the excipients; known morphine sensitivity
  • Respiratory depression; obstructive airways disease; acute asthma exacerbations
  • Acute hepatic disease; acute alcoholism
  • Head injuries; coma; increased intracranial pressure; convulsive disorders
  • Paralytic ileus
  • Concurrent administration with monoamine oxidase inhibitors, or within two weeks of discontinuing them
  • Phaeochromocytoma (morphine and some other opioids can induce endogenous histamine release and thereby stimulate catecholamine release)

Side effects

  • Respiratory depression — the most serious adverse reaction; central sleep apnoea syndrome also reported
  • Nausea and vomiting
  • Constipation (may require appropriate laxatives)
  • Drowsiness/somnolence and confusional state
  • Miosis, hypotension, bradycardia or tachycardia, dry mouth, urinary difficulty (dysuria, ureteric spasm, oliguria)
  • Drug dependence, drug tolerance and drug withdrawal syndrome; allodynia and hyperalgesia

Interactions

  • Monoamine oxidase inhibitors — concurrent use, or use within two weeks of stopping an MAOI, is contraindicated (UK SPC §4.3)
  • Benzodiazepines and other CNS depressants (sedatives/hypnotics, anxiolytics, tranquillisers, muscle relaxants, general anaesthetics, antipsychotics, other opioids, alcohol) — additive effect increases the risk of hypotension, respiratory depression, profound sedation, coma and death; limit dose and duration if concomitant use is warranted (US label §7)
  • Serotonergic drugs — concomitant use with opioids carries a risk of serotonin syndrome (US label §7)

Clinical monograph

How it works

It is an agonist at mu-opioid receptors in the central nervous system, reducing the perception of and emotional response to pain.

Prescribing in practice

  • Titrate carefully and observe for respiratory depression and sedation, particularly with parenteral dosing, in the elderly, and alongside other sedatives.
  • Reduce dose and frequency in renal impairment, as the active metabolite morphine-6-glucuronide accumulates and prolongs effect.
  • Co-prescribe laxatives and antiemetic cover, and plan a step-down analgesic strategy to limit opioid duration.

Monitoring

Monitor pain scores, sedation and respiratory rate after dosing, with naloxone available for over-sedation.

Counselling the patient

  • May cause drowsiness; do not drive or operate machinery if affected.
  • Constipation is common, so take any prescribed laxative regularly.
  • Do not drink alcohol while taking this medicine.

Evidence & guidelines

Strong opioids are recommended for short-term severe acute pain in UK guidance, with emphasis on minimising duration and arranging review.

Reference: NICE NG124 (Hip Fracture); MHRA Drug Safety Update 2017 (Gabapentinoids + Opioids); ERAS Society Guidelines; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.