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 analog presented as a sublingual tablet for sublingual use. It mimics antidiuretic hormone activity to reduce excessive urine production, and is indicated for central diabetes insipidus and nocturnal enuresis in children and adolescents.

GNH India supplies Nocdurna as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing EU‑origin quality for global distribution and ensuring regulatory compliance and reliable supply chains.

Manufacturer / TM Owner

Ferring Lääkkeet Oy

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Indications & Clinical Uses

Desmopressin acts on the antidiuretic hormone pathway to manage conditions characterized by excessive urine output.

  • Central diabetes insipidus: reduces polyuria by enhancing water reabsorption in the kidneys.
  • Nocturnal enuresis (bedwetting) in children and adolescents: decreases nighttime urine volume, helping achieve dry nights.
  • Mild hemophilia A or von Willebrand disease: raises plasma factor VIII and von Willebrand factor levels to improve clotting.

How It Works

  • Desmopressin is a synthetic analogue of vasopressin that selectively binds to V2 receptors on the basolateral membrane of renal collecting‑duct cells. Receptor activation stimulates adenylate cyclase, increasing intracellular cAMP, which promotes insertion of aquaporin‑2 water channels into the apical membrane, thereby enhancing water reabsorption and concentrating urine.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain in the head.
  • Nausea: feeling of queasiness.
  • Nasal congestion: sensation of a blocked nose.

Serious or Rare Side Effects

  • Severe hyponatremia: marked sodium depletion that can cause seizures or coma.
  • Water intoxication: excessive water retention leading to cerebral edema.
  • Allergic reaction: rash, itching, swelling, or anaphylaxis.

Precautions & Warnings

When prescribing Desmopressin, several safety considerations should be observed.

  • Dose titration: start with the lowest effective dose and adjust based on clinical response.
  • Fluid restriction: limit excessive fluid intake to reduce risk of hyponatremia.
  • Monitor electrolytes: regularly check serum sodium and osmolality during therapy.
  • Renal function: assess kidney function before initiating and during treatment.
  • Concomitant ADH‑active drugs: avoid simultaneous use of other antidiuretic agents without supervision.
  • Store at ambient temperature: keep below 25°C in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Desmopressin can interact with several medication classes, requiring careful management.

Major Interactions (Avoid)

  • Other antidiuretic agents (e.g., carbamazepine, chlorpropamide): may cause profound hyponatremia.
  • NSAIDs (e.g., ibuprofen, naproxen): can potentiate water retention and hyponatremia.
  • Certain antidepressants (e.g., SSRIs, SNRIs): increase risk of hyponatremia.

Moderate Interactions (Monitor Closely)

  • Diuretics (especially thiazides): may exacerbate electrolyte disturbances.
  • Opioids (e.g., morphine): can enhance antidiuretic effect.
  • CYP2C9 substrates: desmopressin is minimally metabolised but monitor for altered levels.

Frequently Asked Questions

Nocdurna is prescribed for central diabetes insipidus, a disorder causing excessive urine output, and for nocturnal enuresis (bedwetting) in children and adolescents. It may also be used in mild hemophilia A or von Willebrand disease to improve clotting factor levels.

Desmopressin mimics the natural antidiuretic hormone vasopressin. It binds selectively to V2 receptors in the kidney’s collecting ducts, triggering a cascade that inserts aquaporin‑2 water channels into the cell surface, allowing more water to be reabsorbed and reducing urine volume.

The appropriate dose of Nocdurna is individualized by the prescribing clinician based on the patient’s age, weight, severity of the condition, and response to therapy. No standard dosing regimen is provided here; the prescriber sets the regimen.

Safety data for Nocdurna in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits against possible risks and discuss use with a qualified professional before prescribing to pregnant or nursing individuals.

To request Nocdurna, 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 and any necessary import documentation.

Nocdurna (desmopressin) is a synthetic vasopressin analogue that offers a more selective V2‑receptor profile than older antidiuretic agents, resulting in fewer cardiovascular effects. It is available as a convenient sublingual tablet, whereas some alternatives require nasal spray or injectable forms.

Nocdurna should be stored at ambient temperature, below 25 °C, in its original blister pack. Keep the tablets away from moisture, direct sunlight, and excessive heat to maintain potency throughout the 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, ensuring rapid absorption through the oral mucosa.

The most serious adverse events involve severe hyponatremia and water intoxication, which can lead to seizures, coma, or cerebral edema. Prompt monitoring of serum sodium and fluid intake is essential to mitigate these risks.

Nocdurna is contraindicated in patients with known hypersensitivity to desmopressin, uncontrolled hyponatremia, or conditions predisposing to water retention such as severe heart failure, uncontrolled hypertension, or active pulmonary edema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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