Registered Kenya · PPB

SANDOSTATIN® LAR 20MG INJ

OCTREOTID

H2016/CTD1761/565 20MG NEW/INNOVATOR

What it does

Octreotide is a medication used to treat certain hormone-related conditions.

Commonly used for: Acromegaly, Carcinoid syndrome, VIPoma

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
H2016/CTD1761/565
Registration date
-
Expiry date
-
Status
Registered
Active ingredient
OCTREOTID
Dosage form
20MG
Strength
-
Pack size
1 VIAL
Therapeutic class
NEW/INNOVATOR
Manufacturer / MAH
Nvs Kenya
Applicant / LTR
NOVARTIS PHARMA
Country of origin
FOREIGN
Manufacturer location
Mogadishu Road, off Lunga Lunga Road, Industrial Area, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-01-28 20:31:31 · updated 2026-07-26 11:22:12

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.

About this medicine

Octreotide is a medication used to treat certain hormone-related conditions.

What it treats

  • Acromegaly
  • Carcinoid syndrome
  • VIPoma

How it works

Octreotide works by mimicking a natural hormone that helps to regulate various functions in the body, particularly the release of other hormones.

Who it's for

This medication is for adults and children with specific hormone disorders.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: octreotid

Octreotide is a synthetic analogue of somatostatin, a peptide hormone that inhibits the secretion of various other hormones and substances in the body. It is primarily used in the management of acromegaly, certain types of neuroendocrine tumors, and to control symptoms associated with vasoactive intestinal peptide secreting tumors (VIPomas). It acts by mimicking the action of somatostatin and is administered via subcutaneous or intravenous routes.

Indications

  • Acromegaly
  • Neuroendocrine tumors
  • VIPomas
  • Symptomatic treatment of carcinoid syndrome
  • Prevention of complications after pancreatic surgery

Dosage

Children: Dosing in children should be determined on an individual basis by a specialist, and it is important to refer to the BNF for Children for specific dosing guidelines.

Adults: The initial dose for acromegaly is typically 50 micrograms subcutaneously three times daily, which may be adjusted based on response and tolerability. For other indications, dosing may vary and should be guided by clinical judgment and BNF recommendations.

Mechanism of action

Octreotide exerts its effects by binding to somatostatin receptors, primarily subtype 2 (SSTR2), located in various tissues. This binding inhibits the secretion of growth hormone, insulin, glucagon, and other hormones. Additionally, octreotide reduces gastrointestinal motility and decreases splanchnic blood flow, which can help manage conditions associated with excessive hormone secretion.

Pharmacodynamics

The pharmacodynamic effects of octreotide include the suppression of growth hormone release, inhibition of insulin and glucagon secretion, and a reduction in gastrointestinal secretions and motility. These effects help in treating conditions characterized by hormone overproduction and provide symptomatic relief in certain gastrointestinal disorders.

Pharmacokinetics

Octreotide has a half-life of approximately 1.5 to 2 hours. It is primarily metabolized by the liver and excreted in urine. The bioavailability of subcutaneously administered octreotide is about 60% and is affected by the site of injection. Steady-state concentrations are typically achieved within 24 hours of administration.

Adverse effects

  • Gastrointestinal disturbances (nausea, vomiting, diarrhea)
  • Abdominal pain
  • Fatigue
  • Injection site reactions
  • Gallbladder abnormalities
  • Hyperglycemia

Interactions

  • octreotide+oral ciclosporin: Unknown (decreases absorption)
  • octreotide+telotristat ethyl: Unknown (decreases exposure)

Precautions

  • Caution in patients with diabetes mellitus due to potential hyperglycemia.
  • Monitor thyroid function as octreotide can affect thyroid hormone levels.
  • Use with caution in patients with gallbladder disease.

Pregnancy

Octreotide is classified as pregnancy category B. Animal studies have not shown any adverse effects, but there are no adequate and well-controlled studies in pregnant women.

Breast-feeding

Octreotide is excreted in breast milk. Caution is advised when administering to nursing mothers.

Storage

Store in a refrigerator (2°C to 8°C). Do not freeze. Protect from light.

Formulations

  • Injectable solution (subcutaneous or intramuscular)
  • Long-acting release formulation

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.