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Somatostatin: Brands, Price & Uses in Bangladesh

Somatostatin is a synthetic cyclic peptide identical to the naturally occurring hormone somatostatin-14.

Forms:IV Injection

About Somatostatin

Indications of Somatostatin

Somatostatin is a synthetic cyclic peptide identical to the naturally occurring hormone somatostatin-14. It is administered as a continuous intravenous infusion under hospital supervision for the following indications, classified by strength of evidence:

Established, guideline-supported uses

  • Bleeding oesophageal and gastric varices - Somatostatin is used, together with endoscopic therapy, to control acute variceal bleeding in patients with portal hypertension (e.g., cirrhosis). This use is supported by international consensus guidelines on portal hypertension, and Somatostatin/its analogues are included in resource protocols for variceal haemorrhage.
  • Severe upper gastrointestinal bleeding (e.g., bleeding peptic ulcer) - used as an adjunct to endoscopic haemostasis to reduce gastric acid and splanchnic blood flow while definitive treatment is arranged.

Adjunctive / supportive uses

  • Pancreatic and enterocutaneous (intestinal) fistulas - Somatostatin reduces pancreatic exocrine and intestinal secretions, which can decrease fistula output and support closure, usually alongside nutritional support and surgical management.
  • Prevention of complications after pancreatic surgery - used peri-operatively in some centres to reduce pancreatic secretion and the risk of post-operative pancreatic fistula.

Off-label / less-established uses

  • Adjunct in acute pancreatitis to reduce pancreatic secretion, although evidence for a clear outcome benefit is limited and this is not a standard first-line indication.

Somatostatin is always used under close medical/hospital supervision as a continuous intravenous infusion; it is not intended for outpatient or self-administered use.

Dosage & Administration of Somatostatin

Somatostatin is given only by continuous intravenous infusion, in hospital, with cardiac and glucose monitoring. Typical adult dosing by indication is summarised below; the treating physician individualises the exact regimen.

IndicationTypical adult doseTypical duration
Bleeding oesophageal/gastric varicesInitial slow IV bolus of 250 micrograms over 3-5 minutes, followed by continuous IV infusion of 250 micrograms/hour (approximately 3.5 micrograms/kg/hour)Usually continued for 48-120 hours, or until bleeding is controlled for at least 24 hours, as directed by the physician
Severe upper GI bleeding (e.g., bleeding peptic ulcer)Same regimen as above (250 microgram bolus then 250 micrograms/hour infusion), used with endoscopic therapyUntil haemostasis is confirmed and the physician determines the infusion can be stopped
Pancreatic/intestinal fistulaContinuous IV infusion of 250 micrograms/hour (may be adjusted based on fistula output)Continued for days to a few weeks until fistula output decreases substantially, alongside nutritional and surgical management

Renal/hepatic impairment

There is no well-established, standardised dose-adjustment schedule for renal or hepatic impairment; Somatostatin should be used with caution and closer monitoring in these patients, as clearance may be reduced (see Precautions and Warnings).

Interrupted infusion

Because Somatostatin is given as a continuous hospital infusion, dosing is managed entirely by the treating medical team; there is no patient-administered "missed dose" scenario.

Side Effects of Somatostatin

Somatostatin is generally used for short periods under hospital monitoring; reported adverse effects include:

Common

  • Nausea, vomiting, abdominal cramping or bloating
  • Flushing of the face
  • Dizziness or headache
  • Hyperglycaemia or hypoglycaemia (see Precautions and Warnings)
  • Injection/infusion site reactions

Less common/serious

  • Bradycardia and other cardiac rhythm disturbances
  • Gallstone formation or biliary sludge with prolonged use
  • Rare hypersensitivity reactions

Patients should be monitored for these effects throughout the infusion, and any severe or persistent symptoms should be reported to the treating physician immediately.

Contraindications of Somatostatin

Somatostatin is contraindicated in patients with known hypersensitivity to Somatostatin or any component of the formulation. There are no other well-established absolute contraindications; conditions such as pregnancy, diabetes, or cardiac disease require caution and closer monitoring rather than being absolute contraindications (see Precautions and Warnings, and Pregnancy and Lactation).

Frequently Asked Questions about Somatostatin

What is Somatostatin used for?

Somatostatin is used mainly in hospital to control severe gastrointestinal bleeding, such as bleeding from oesophageal/gastric varices or peptic ulcers, and to reduce secretions in certain pancreatic or intestinal fistulas. It is given only as a continuous intravenous infusion under close medical supervision.

How is Somatostatin given?

Somatostatin is given by a doctor or nurse as an intravenous infusion, usually starting with a slow bolus injection followed by a continuous infusion using an infusion pump. It is not taken by mouth and is not for home use.

What are the common side effects of Somatostatin?

Common side effects include nausea, vomiting, abdominal cramping, flushing, dizziness, and changes in blood sugar (either high or low). Your care team will monitor you closely for these effects during treatment.

Can Somatostatin be used during pregnancy?

Data on Somatostatin use in pregnancy are limited, and it may reduce blood flow to the placenta, so it should be used in pregnancy only if the potential benefit clearly outweighs the potential risk, and only under close specialist supervision.

Who should not receive Somatostatin?

Somatostatin should not be given to anyone with a known hypersensitivity (allergy) to Somatostatin or any component of the injection. Patients with diabetes or heart problems can still receive it but need closer monitoring rather than avoiding it altogether.

What happens if too much Somatostatin is given?

An overdose could worsen effects such as low or high blood sugar, a slow heart rate, flushing, nausea, or vomiting. Because Somatostatin is only given in hospital with continuous monitoring, the infusion would be stopped or adjusted immediately and supportive treatment given; if overdose is suspected outside such a setting, emergency medical help or a poison control centre should be contacted right away.

Disclaimer

The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.

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