Product image of Olatuton (Octreotide Acetate) supplied by GNH India

Olatuton

Active Ingredient:
Octreotide Acetate
Origin:
EU

Olatuton (Octreotide Acetate)

Octreotide Acetate, the active ingredient in Olatuton, is a somatostatin analog presented as a strength/form for intramuscular use. It treats hormone‑secreting tumors and related endocrine disorders in adults. GNH India supplies Olatuton as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and oncology centres worldwide.

GNH India supplies Olatuton as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and oncology centres worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Olatuton is a somatostatin analog that modulates hormone‑secretion pathways in several endocrine conditions.

  • Acromegaly: reduces excess growth‑hormone production and helps control disease activity.
  • Neuroendocrine tumours: controls tumour‑related hormone secretion and alleviates flushing and diarrhoea.
  • Carcinoid syndrome: diminishes flushing, wheezing and diarrhoea associated with serotonin excess.
  • VIPoma: lowers vasoactive intestinal peptide levels and reduces severe watery diarrhoea.
  • Post‑operative pancreatic fistula prevention: decreases pancreatic secretions after major abdominal surgery.

How It Works

  • Octreotide acetate binds with high affinity to somatostatin receptors (mainly sst2 and sst5) on endocrine cells, inhibiting cyclic AMP formation and calcium influx. This receptor activation suppresses the release of several hormones—including growth hormone, insulin, glucagon, gastrin and vasoactive intestinal peptide—thereby reducing hormone‑driven clinical effects.

Side Effects

Adverse reactions to Olatuton are generally related to its hormonal inhibition and injection‑site tolerability.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Abdominal pain: cramp‑like discomfort.
  • Diarrhoea or constipation: altered bowel habits.
  • Injection‑site reactions: redness, swelling or bruising.
  • Headache: transient head discomfort.
  • Hyperglycaemia: elevated blood‑sugar levels.

Serious or Rare Side Effects

  • Gallbladder disease: sludge or stones leading to biliary colic.
  • Pancreatitis: inflammation of the pancreas.
  • Severe hypoglycaemia: dangerously low blood‑sugar, especially in diabetic patients.
  • Cardiac arrhythmias: irregular heart rhythm.
  • Anaphylaxis: acute allergic reaction requiring immediate medical care.

Precautions & Warnings

When using Olatuton, clinicians should assess patient‑specific factors and monitor for known risks.

  • Cardiovascular assessment: evaluate for existing heart disease before initiating therapy.
  • Glycaemic monitoring: check blood‑glucose levels in diabetic or pre‑diabetic patients.
  • Gallbladder evaluation: consider ultrasound screening for patients with a history of gallstones.
  • Pregnancy and lactation: avoid unless the potential benefit outweighs risk.
  • Renal or hepatic impairment: adjust monitoring frequency as organ function may affect drug clearance.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Octreotide may interact with several medicines that influence hormone levels or gastrointestinal motility.

Major Interactions (Avoid)

  • Insulin or oral hypoglycaics: may potentiate hypoglycaemia.
  • Cytochrome P450 3A4 inducers: can reduce octreotide exposure.

Moderate Interactions (Monitor Closely)

  • Somatostatin analogues other than Olatuton: additive hormonal suppression.
  • Proton‑pump inhibitors: may alter gastric pH and affect absorption of concomitant oral agents.
  • Antiplatelet or anticoagulant drugs: increased risk of injection‑site bleeding.

Frequently Asked Questions

Olatuton contains octreotide acetate, a somatostatin analogue that is prescribed to control hormone‑secreting tumours such as acromegaly, neuroendocrine tumours, carcinoid syndrome and VIP‑related diarrhoea, and to reduce pancreatic secretions after major abdominal surgery.

Octreotide acetate binds to somatostatin receptors (mainly sst2 and sst5) on endocrine cells, blocking cyclic AMP formation and calcium influx, which suppresses the release of growth hormone, insulin, glucagon, gastrin and vasoactive intestinal peptide.

The dose of Olatuton is individualized by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and treatment response. Exact dosing regimens are not provided here.

Octreotide acetate is classified as pregnancy‑category B in the EU, indicating no proven risk in animal studies but limited human data. It should only be used if the potential benefit justifies the potential risk to the fetus, and breastfeeding is generally not recommended while on therapy.

To order Olatuton, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Olatuton (octreotide acetate) is chemically similar to other octreotide formulations and to lanreotide, another long‑acting somatostatin analogue. All share the same receptor profile, but differences exist in dosing frequency, formulation (short‑acting vs. long‑acting depot) and injection site, which can influence convenience and patient preference.

Olatuton should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.

Olatuton is supplied for parenteral use and is administered by subcutaneous or intramuscular injection, typically by a healthcare professional. The injection site should be rotated and aseptic technique observed.

Serious adverse events include gallbladder disease (sludge or stones), pancreatitis, severe hypoglycaemia, cardiac arrhythmias and anaphylactic reactions. Patients should be monitored regularly for these conditions, especially if they have pre‑existing risk factors.

Olatuton is contraindicated in patients with known hypersensitivity to octreotide or any excipients in the formulation, and it should be used with caution in individuals with uncontrolled diabetes, severe cardiac disease, or active gallbladder pathology.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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