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Octreotide

Somatostatin analogue · Antidiarrheal

Also known as Sandostatin, Sandostatin LAR, Octreotide acetate

START
IR 50 mcg SC 1–2×/day, titrate; variceal bleed 50 mcg IV bolus + 50 mcg/h
TYPICAL MAX
~1500 mcg/day SC; LAR 40 mg q4 weeks
STOP IF
Symptomatic bradyarrhythmia, biliary obstruction, severe glycaemic instability
WATCH
Glucose, gallbladder US (chronic), thyroid, heart rate
CDSCO approvedSchedule HATC H01CB02
Dose laddermg/d
0.05start0.3titrate1.5max40ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLUsual dosing30REDUCEReduce LAR starting dose (reduced cl…90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
6minONSET24minPEAK1.7h8hDURATION
ONSET
6min · absorption onset
PEAK
24min · SC Cmax
1.7h · SC t½
DURATION
8h · IR effect
EXCRETION
~32% renal unchanged; hepatic + faecal
route + CYP
INTERACTIONS
6 major
SEVERE in our sources
PREGNANCY
Use only if clearly needed — limited human data
FDA category + note
Top interactionssee all 9
  • BexaroteneSevereDatabaseDDInter
  • LonafarnibSevereDatabaseDDInter
  • CiclosporinSevereDatabaseKimi deep-research + Cla
  • InsulinSevereDatabaseKimi deep-research + Cla
Available in India

56 branded formulations. Look up specific brands in the Drugs workspace.

Mechanism

Long-acting somatostatin analogue; binds somatostatin receptors (mainly SSTR2/5) to suppress GH/IGF-1, glucagon, insulin, gastrin, VIP, serotonin and splanchnic blood flow.

Indications

AcromegalyCarcinoid syndrome and VIPoma symptom controlVariceal/GI bleeding (acute, off-label widely used)Refractory diarrhoea (e.g. chemotherapy, AIDS); pancreatic fistula

Dosing

Adult
Immediate-release: 50 mcg SC 1–2×/day, titrate to 100–600 mcg/day divided (max ~1500 mcg/day). Acromegaly LAR: 20 mg IM q4 weeks. Variceal bleed: 50 mcg IV bolus then 50 mcg/h infusion 2–5 days.
Pediatric
1–10 mcg/kg/day SC (e.g. hyperinsulinaemic hypoglycaemia); specialist.
Renal adjustment
Reduce LAR starting dose in severe renal impairment/dialysis (clearance reduced).
Hepatic adjustment
Cirrhosis: clearance reduced — adjust maintenance dose.
Geriatric
May need dose adjustment (reduced clearance).
Max dose
~1500 mcg/day SC (symptom control); LAR 40 mg q4 weeks

Pharmacokinetics

Onset
SC ~30 min
Peak effect
SC ~0.4 h; LAR plateau ~2–3 weeks
Duration
SC ~6–12 h; LAR ~4 weeks
Half-life
SC ~1.7 h; LAR apparent ~weeks
Bioavailability
SC ~100%
Protein binding
~65% (lipoprotein)
Metabolism
Hepatic; some renal
Excretion
~32% renal unchanged; faecal

Contraindications

  • Hypersensitivity to octreotide

Side effects

Common
Injection-site painGI: diarrhoea, abdominal cramps, flatulence, steatorrhoeaNauseaHyper- or hypoglycaemia
Serious
  • Gallstones/biliary sludge with chronic use
  • Symptomatic bradycardia/arrhythmia
  • Severe hypo/hyperglycaemia
  • Hypothyroidism (chronic); pancreatitis

Pregnancy & lactation

Pregnancy

Use only if clearly needed — limited human data

Lactation

Unknown excretion; avoid or monitor infant

Drug interactions

Bexarotene
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Lonafarnib
Severe
Database

Clinical effect not specified

Source: DDInter

Ciclosporin
Severe
Database

Reduced ciclosporin absorption → graft rejection risk

Monitor ciclosporin levels, adjust dose

Source: Kimi deep-research + Cla

Insulin
Severe
Database

Altered glucose counter-regulation → hypo- or hyperglycaemia

Monitor glucose closely; adjust antidiabetic dose

Source: Kimi deep-research + Cla

Pexidartinib
Severe
Database

Clinical effect not specified

Source: DDInter

Telotristat Ethyl
Severe
Database

Clinical effect not specified

Source: DDInter

Bromocriptine
Moderate
Database

Increased bromocriptine availability

Monitor for dopaminergic adverse effects

Source: Kimi deep-research + Cla

Oral Drugs
Moderate
Database

Altered GI motility/absorption

Monitor efficacy of narrow-index oral drugs

Source: Kimi deep-research + Cla

Qt Prolonging Drugs
Moderate
Database

Bradycardia/QT effects additive

ECG monitoring with class III antiarrhythmics etc.

Source: Kimi deep-research + Cla

3 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Ask House about Octreotide

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19