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Gastrointestinal Emergency Pregnancy: §4.6: limited data (fewer than 300 pregnancy outcomes); congenital anomalies were reported in about 4% of pregnancy cases with a known outcome, with no causal relationship to octreotide suspected. As a precautionary measure it is preferable to avoid the use of octreotide during pregnancy. It is unknown whether octreotide is excreted in human breast milk (it is excreted in animal milk); patients should not breast-feed during treatment.

Octreotide

Brand names: Sandostatin

Used in: Gastrointestinal Bleeding

Octreotide is a somatostatin analogue used in emergencies to reduce splanchnic blood flow in variceal and other gastrointestinal bleeding, and longer term in certain neuroendocrine and secretory conditions. In acute bleeding it is given by intravenous infusion.

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: Bleeding gastro-oesophageal varices: 25 micrograms/hour for 5 days by continuous intravenous (i.v.) infusion.
Route: Continuous intravenous infusion (after dilution; octreotide can be used in dilution with physiological saline)
Frequency: Continuous infusion, for 5 days
Max: 50 micrograms/hour — §4.4: 'The maximum dose of 50 microgram/hour should therefore not be exceeded.' Atrioventricular blocks (including complete atrioventricular block) were reported in patients receiving high doses of continuous infusion (100 micrograms/hour) and in patients receiving bolus octreotide intravenously (50 micrograms bolus followed by 50 micrograms/hour continuous infusion). Patients who receive high doses of intravenous octreotide should be kept under appropriate cardiac monitoring.
UK SPC for Octreotide 100 microgram/ml solution for injection/infusion (immediate-release). This id is the emergency-medicine entry and therefore leads with the acute indication in §4.2, bleeding gastro-oesophageal varices; the bundle's name field carries only the generic 'Octreotide'. The dose above is an HOURLY INFUSION RATE in micrograms/hour — it is not a bolus and not a subcutaneous dose. CIRRHOTIC PATIENTS: 'In cirrhotic patients with bleeding gastro-oesophageal varices, Octreotide has been well tolerated at continuous i.v. doses of up to 50 micrograms/hour for 5 days' — the §4.4 ceiling of 50 micrograms/hour still applies. HEPATIC IMPAIRMENT (directly relevant here, as most patients treated for variceal bleeding are cirrhotic): in patients with liver cirrhosis the half-life of the drug may be increased, necessitating adjustment of the maintenance dosage. OTHER LICENSED INDICATIONS: §4.2 also covers acromegaly, gastro-entero-pancreatic endocrine tumours, complications following pancreatic surgery and TSH-secreting pituitary adenomas — all SUBCUTANEOUS regimens in micrograms per injection, on a different route and a different unit basis from the infusion rate above. Their figures are deliberately NOT reproduced on this emergency page to avoid a subcutaneous dose being read as an infusion rate; see the general octreotide entry. PAEDIATRIC: 'Experience with Octreotide in children is limited' — the SPC states no paediatric dose, so none is recorded here; verify any under-18 use against a children's formulary. MONITORING (§4.4): patients on high-dose intravenous octreotide need appropriate cardiac monitoring; octreotide may affect glucose regulation (both hyperglycaemia and hypoglycaemia are reported); thyroid and hepatic function should be monitored during prolonged treatment, and gallbladder ultrasound is recommended before and at about 6- to 12-month intervals during longer-term therapy.

Dose adjustments

Renal

§4.2: 'Impaired renal function did not affect the total exposure (AUC) to octreotide administered as s.c. injection, therefore no dose adjustment of Octreotide is necessary.'

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.

US labelling (FDA)

Reference — US labelling, may differ from UK

Octreotide Acetate injection may be administered subcutaneously or intravenously. ( 2.1 ) Acromegaly : Recommended initial Octreotide Acetate injection dosage is 50 mcg three times daily during the initial 2 weeks of therapy. Maintenance dose 100 mcg to 500 mcg three times daily. ( 2.2 ) Carcinoid Tumors : Recommended dosage range of 100 mcg to 600 mcg daily in two to four divided doses during the initial 2 weeks of therapy. ( 2.3 ) VIPomas : Recommended dosage range of 200 mcg to 300 mcg daily in two to four divided doses during the initial 2 weeks of therapy. ( 2.4 ) 2.1 Dosage and Administration Overview Octreotide Acetate injection may be administered subcutaneously or intravenously. …

Source: US FDA prescribing information (openFDA / DailyMed), label dated 2025-01-16. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.

Contraindications

  • Known hypersensitivity to the active substance or to any of the excipients (§4.3)

Side effects

  • Common — cardiac: bradycardia (uncommon: tachycardia); §4.4 additionally reports atrioventricular block, including complete AV block, with high-dose intravenous administration
  • Very common — gastrointestinal: diarrhoea, abdominal pain, nausea, constipation, flatulence
  • Very common — hyperglycaemia; common: hypoglycaemia and impaired glucose tolerance
  • Very common — cholelithiasis; common: cholecystitis, biliary sludge, hyperbilirubinaemia
  • Very common — headache and injection site reactions; common: dizziness and asthenia

Interactions

  • SOURCE NOTE: UK SPC §4.5 was not captured in this bundle. Except where marked, the entries below are from the US prescribing information §7 (Meitheal octreotide acetate injection) and must be verified against §4.5 of the UK SPC.
  • Bradycardia-inducing medicines — UK SPC §4.4: common cases of bradycardia have been reported and dose adjustment of medicinal products such as beta blockers, calcium channel blockers, or agents to control fluid and electrolyte balance may be necessary
  • Insulin and oral hypoglycaemic drugs — octreotide inhibits the secretion of insulin and glucagon; monitor blood glucose when treatment is initiated or the dose is altered and adjust anti-diabetic treatment accordingly (US §7.2)
  • Ciclosporin (cyclosporine) — concomitant administration may decrease blood levels of ciclosporin and result in transplant rejection (US §7.1)
  • Bromocriptine — concomitant administration increases the availability of bromocriptine (US §7.3)
  • Lutetium Lu 177 dotatate injection — discontinue octreotide at least 24 hours prior to each lutetium Lu 177 dotatate dose (US §7.6)

Clinical monograph

How it works

It mimics the action of somatostatin, inhibiting the release of several gut and pituitary hormones and reducing splanchnic and portal blood flow, which helps control variceal haemorrhage.

Prescribing in practice

  • It can disturb glucose control, causing either hyperglycaemia or hypoglycaemia, so blood glucose should be monitored, particularly in people with diabetes.
  • Long-term use predisposes to gallstones, so periodic gallbladder assessment is advised with prolonged therapy.
  • It can slow the heart and cause bradycardia, warranting caution in those with cardiac conduction problems.

Monitoring

During acute use monitor blood glucose, heart rate and the clinical response to bleeding; with long-term therapy add periodic gallbladder imaging and thyroid and other relevant endocrine assessment as indicated.

Counselling the patient

  • Report symptoms of high or low blood sugar, such as marked thirst, drowsiness, sweating or shakiness.
  • Report abdominal pain, which may indicate gallstones with longer-term treatment.
  • Report palpitations or feeling that the heart is beating slowly.

Evidence & guidelines

Used as an adjunct in the management of acute variceal bleeding and in selected neuroendocrine and secretory disorders.

Reference: BAVENO VII Consensus 2022; NEJM 1995; 333(9):555-560; BSG Variceal 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.

📚 MRCEM Revision

Featured in these MRCEM clinical pathways

Octreotide is a core drug in the following exam-focused workups on our sister siteReviseMRCEM.

MRCEM Primary / Intermediate / OSCE candidates: each pathway includes exam-style questions, RCEM/NICE citations, and FAQ summaries.