Product image of Mitaclau (Desmopressin) supplied by GNH India

Mitaclau

Active Ingredient:
Desmopressin
Origin:
EU

Mitaclau (Desmopressin)

Desmopressin, the active ingredient in Mitaclau, is a vasopressin analog (antidiuretic hormone) presented as a sublingual formulation for sublingual use. It is employed to manage central diabetes insipidus, nocturnal enuresis, and certain bleeding disorders by enhancing water reabsorption and promoting clotting factor release.

GNH India supplies Mitaclau as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Norameda Uab

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Indications & Clinical Uses

Mitaclau acts on the vasopressin V2 receptor pathway to control water balance and support haemostasis.

  • Central diabetes insipidus: reduces excessive urine output and stabilises plasma osmolality.
  • Nocturnal enuresis: decreases nighttime urinary frequency in children and adults.
  • Hemophilia A: raises factor VIII levels to improve clot formation.
  • Von Willebrand disease: enhances von Willebrand factor release, aiding platelet adhesion and clot stability.

How It Works

  • Desmopressin selectively stimulates vasopressin V2 receptors in the renal collecting ducts, promoting insertion of aquaporin‑2 water channels and increasing water reabsorption. In the vascular endothelium, it triggers release of stored factor VIII and von Willebrand factor, thereby augmenting the coagulation cascade and improving haemostatic function.

Side Effects

Desmopressin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Nasal congestion or irritation (if administered intranasally).
  • Nausea or abdominal discomfort.
  • Mild hyponatraemia: low sodium levels without severe symptoms.
  • Flushing or warmth sensation.
  • Dizziness or light‑headedness.

Serious or Rare Side Effects

  • Severe hyponatraemia: can lead to seizures, coma, or cerebral oedema.
  • Water intoxication: excessive fluid retention causing rapid weight gain.
  • Allergic reactions: rash, itching, or anaphylaxis.
  • Thrombotic events: rare clot formation in predisposed individuals.
  • Cardiac arrhythmias: associated with electrolyte disturbances.
  • Hypertension: sudden increase in blood pressure.

Precautions & Warnings

Before using Mitaclau, consider the following safety measures.

  • Assess fluid balance: monitor intake and output to avoid water overload.
  • Check serum sodium: baseline and periodic testing are recommended, especially in the elderly.
  • Review concomitant medications: avoid drugs that may exacerbate hyponatraemia, such as thiazide diuretics.
  • Caution in renal impairment: dose adjustments may be required.
  • Pregnancy and lactation: discuss potential risks with a healthcare professional.
  • Store below 25°C: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Desmopressin can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Concomitant use with vasopressin antagonists (e.g., conivaptan) may negate therapeutic effect.
  • Co‑administration with carbamazepine or phenytoin can markedly reduce plasma levels.

Moderate Interactions (Monitor Closely)

  • NSAIDs (e.g., ibuprofen) may increase risk of hyponatraemia.
  • Loop or thiazide diuretics can potentiate water‑electrolyte disturbances.
  • Antihypertensives (e.g., ACE inhibitors) may enhance hypotensive effects.
  • Antidepressants (e.g., SSRIs) may contribute to electrolyte imbalance.

Frequently Asked Questions

Mitaclau is prescribed for central diabetes insipidus to control excessive urination, nocturnal enuresis to reduce nighttime bedwetting, hemophilia A to raise factor VIII levels, and von Willebrand disease to increase von Willebrand factor and improve clotting.

Desmopressin acts as a selective agonist at vasopressin V2 receptors in the kidneys, promoting insertion of aquaporin‑2 channels and enhancing water reabsorption. It also stimulates endothelial cells to release factor VIII and von Willebrand factor, supporting haemostasis.

The appropriate dose of Mitaclau is determined by the prescribing clinician based on the specific indication, patient age, weight, renal function, and response to therapy. Dosage regimens are individualized and should follow the prescriber’s instructions.

Safety data for Mitaclau in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits against possible risks and discuss any concerns with the patient before initiating therapy.

To place an order, submit an enquiry on the Mitaclau 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 and any necessary import documentation.

Mitaclau (desmopressin) is a synthetic analogue of vasopressin with a longer half‑life and greater selectivity for V2 receptors, offering more predictable water‑retaining effects and fewer vasoconstrictive actions compared with natural vasopressin. It is generally preferred for chronic management of diabetes insipidus and bleeding disorders.

Mitaclau should be stored below 25 °C in its original packaging, protected from moisture and direct sunlight. Do not refrigerate or freeze the product, and keep it out of reach of children.

Mitaclau is administered sublingually. The tablet is placed under the tongue and allowed to dissolve completely without swallowing, ensuring rapid absorption through the oral mucosa.

The most critical safety concerns are severe hyponatraemia and water intoxication, which can lead to seizures, cerebral oedema, or coma. Patients should be monitored for rapid weight gain, low sodium levels, and neurological symptoms, especially when fluid intake is high.

Mitaclau is contraindicated in patients with known hypersensitivity to desmopressin, uncontrolled hyponatraemia, severe renal impairment, or active uncontrolled hypertension. Caution is also advised for individuals taking medications that predispose to electrolyte disturbances.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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