
Stilamin3 mg/ampou
Janata Traders
Somatostatin is a synthetic cyclic peptide identical to the naturally occurring hormone somatostatin-14.
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:
Somatostatin is always used under close medical/hospital supervision as a continuous intravenous infusion; it is not intended for outpatient or self-administered use.
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.
| Indication | Typical adult dose | Typical duration |
|---|---|---|
| Bleeding oesophageal/gastric varices | Initial 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 therapy | Until haemostasis is confirmed and the physician determines the infusion can be stopped |
| Pancreatic/intestinal fistula | Continuous 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 |
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).
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.
Somatostatin is generally used for short periods under hospital monitoring; reported adverse effects include:
Patients should be monitored for these effects throughout the infusion, and any severe or persistent symptoms should be reported to the treating physician immediately.
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).
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