Product image of Nocdurna (Desmopressin) supplied by GNH India

Nocdurna

Active Ingredient:
Desmopressin
Origin:
EU

Nocdurna (Desmopressin)

Desmopressin, the active ingredient in Nocdurna, is a vasopressin (antidiuretic hormone) analog presented as a sublingual tablet for sublingual use. It selectively stimulates renal V2 receptors to reduce urine output and also raises plasma factor VIII and von Willebrand factor, making it useful for treating nocturnal enuresis in children and adolescents, central diabetes insipidus, and for hemostatic control in hemophilia A and von Willebrand disease.

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

Manufacturer / TM Owner

Ferring Hellas Mepe

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Indications & Clinical Uses

  • Desmopressin acts on the antidiuretic hormone pathway and is indicated for the following conditions:
  • Nocturnal enuresis: Reduces nighttime urine production, helping children and adolescents achieve dry nights.
  • Central diabetes insipidus: Increases water reabsorption in the kidneys to control polyuria and polydipsia.
  • Hemophilia A and von Willebrand disease (hemostatic use): Elevates plasma factor VIII and von Willebrand factor levels to improve clot formation during bleeding episodes or surgical procedures.

How It Works

  • Desmopressin is a synthetic analogue of vasopressin that binds selectively to V2 receptors located on the basolateral membrane of renal collecting‑duct cells. Activation of V2 receptors stimulates adenylate cyclase, raising intracellular cAMP, which promotes insertion of aquaporin‑2 water channels into the apical membrane, enhancing water reabsorption. In the vascular endothelium, the drug stimulates release of factor VIII and von Willebrand factor, contributing to its hemostatic effect.

Side Effects

Desmopressin may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Headache: mild to moderate pain often reported during treatment.
  • Nausea: occasional upset stomach or feeling of queasiness.
  • Nasal congestion: sensation of blocked nasal passages.
  • Dizziness: transient light‑headedness, especially after standing.

Serious or Rare Side Effects

  • Hyponatremia: severe low blood sodium that can lead to seizures or coma.
  • Water intoxication: excessive fluid retention causing swelling or pulmonary edema.
  • Thromboembolic events: rare clot formation in veins or arteries.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.

Precautions & Warnings

When prescribing Desmopressin, clinicians should consider several safety measures and monitoring requirements.

  • Assess fluid balance: monitor intake and output to avoid water overload.
  • Check serum sodium: evaluate baseline and periodic sodium levels, especially in at‑risk patients.
  • Caution in renal impairment: adjust use and monitor kidney function closely.
  • Avoid concomitant hyponatremia‑inducing drugs: limit use with diuretics or certain antidepressants.
  • Use with caution in pregnancy: limited data; weigh benefits against potential risks.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concomitant use of thiazide diuretics: may increase risk of hyponatremia.
  • Co‑administration with carbamazepine: can reduce Desmopressin’s antidiuretic effect.
  • Combined therapy with other antidiuretic agents (e.g., chlorpropamide): heightens water retention risk.

Moderate Interactions (Monitor Closely)

  • NSAIDs (e.g., ibuprofen): may impair renal water handling, requiring sodium monitoring.
  • Selective serotonin reuptake inhibitors (SSRIs): potential additive effect on serum sodium.
  • Anticoagulants (e.g., warfarin): may enhance hemostatic response, monitor clotting parameters.

Frequently Asked Questions

Nocdurna contains desmopressin and is prescribed to manage nocturnal enuresis in children and adolescents, to treat central diabetes insipidus by reducing excessive urine output, and to provide hemostatic support in patients with hemophilia A or von Willebrand disease during bleeding episodes or surgical procedures.

Desmopressin is a synthetic analogue of vasopressin that selectively activates V2 receptors in the renal collecting ducts. This activation raises intracellular cAMP, causing aquaporin‑2 water channels to move to the cell surface, which increases water reabsorption. In the bloodstream, it also stimulates release of factor VIII and von Willebrand factor, enhancing clot formation.

The dose of Nocdurna is individualized by the prescribing healthcare professional based on the patient’s age, weight, underlying condition, renal function, and response to therapy. No fixed regimen is provided here; clinicians adjust the amount to achieve the desired clinical effect while monitoring safety parameters.

Safety data for desmopressin during pregnancy and lactation are limited. The drug should only be used when the potential benefit justifies any possible risk to the fetus or infant. Healthcare providers should discuss individual circumstances and consider alternative therapies when appropriate.

To order Nocdurna, submit an enquiry on the product page at gnhindia.com with 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 any cold‑chain requirements) and the necessary import documentation.

The primary alternative to desmopressin is natural vasopressin (Pitressin) administered intravenously or intranasally. Desmopressin offers a longer half‑life, selective V2 receptor activity, and a convenient sublingual tablet form, which reduces the risk of cardiovascular side effects associated with vasopressin while providing comparable antidiuretic and hemostatic benefits.

Nocdurna tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original blister pack, protect from moisture and direct sunlight, and ensure the container is tightly closed to maintain tablet integrity throughout its shelf life.

Nocdurna is taken as a sublingual tablet. The tablet is placed under the tongue and allowed to dissolve completely without chewing or swallowing whole. Patients should avoid eating or drinking for a few minutes after administration to ensure optimal absorption.

The most serious risks include severe hyponatremia, which can lead to seizures, coma, or death, and water intoxication causing pulmonary edema. Patients should be monitored for sudden changes in weight, headache, nausea, or confusion, and fluid intake should be carefully managed.

Nocdurna is contraindicated in patients with known hypersensitivity to desmopressin, uncontrolled hyponatremia, severe renal impairment, or active pulmonary edema. Caution is also advised for individuals with a history of hyponatremic seizures or those taking medications that significantly affect sodium balance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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