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 is used to manage central diabetes insipidus, nocturnal enuresis, and certain bleeding disorders in appropriate patients.

GNH India supplies Nocdurna as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory‑compliant shipments to global healthcare providers.

Manufacturer / TM Owner

Ferring Lægemidler A/S

1
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Indications & Clinical Uses

Desmopressin is employed in conditions that involve impaired water balance or coagulation deficits.

  • Central diabetes insipidus: reduces excessive urine output by increasing renal water reabsorption.
  • Nocturnal enuresis: decreases nighttime bedwetting episodes through antidiuretic action.
  • Bleeding disorders (e.g., hemophilia A, von Willebrand disease): raises plasma levels of clotting factor VIII and von Willebrand factor to improve hemostasis.

How It Works

  • Desmopressin is a synthetic analogue of vasopressin that selectively activates V2 receptors on the basolateral membrane of renal collecting‑duct cells. V2‑receptor stimulation triggers cyclic AMP formation, promoting insertion of aquaporin‑2 water channels into the apical membrane, thereby enhancing water reabsorption and concentrating urine. In haemostatic indications, it stimulates release of stored factor VIII and von Willebrand factor from endothelial cells.

Side Effects

Desmopressin may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Nausea: occasional, transient.
  • Abdominal cramps: mild discomfort.
  • Facial flushing: transient reddening of skin.

Serious or Rare Side Effects

  • Severe hyponatremia: potentially life‑threatening low sodium levels.
  • Seizures: secondary to profound hyponatremia.
  • Thrombotic events: rare clot formation, especially in predisposed patients.
  • Allergic reactions (anaphylaxis): rare but may be severe.

Precautions & Warnings

When prescribing or dispensing Nocdurna, consider the following safety measures.

  • Monitor serum sodium: check electrolytes regularly, especially in at‑risk patients.
  • Limit fluid intake: advise patients to avoid excessive water consumption to reduce hyponatremia risk.
  • Assess renal function: adjust use in patients with impaired kidney function.
  • Avoid use in uncontrolled hypertension: monitor blood pressure during therapy.
  • Store at ambient temperature: keep in original container, protect from moisture and heat.

Avoid Interactions

Desmopressin can interact with several medicines; awareness of the interaction level helps guide clinical decisions.

Major Interactions (Avoid)

  • Concomitant antidiuretic agents (e.g., oxytocin): risk of severe hyponatremia.
  • Carbamazepine: may reduce desmopressin efficacy.
  • NSAIDs: may potentiate antidiuretic effect and increase hyponatremia risk.

Moderate Interactions (Monitor Closely)

  • Warfarin: may increase bleeding risk in haemophilia patients.
  • Diuretics: may alter fluid and electrolyte balance.
  • CYP‑modulating drugs: limited data, monitor clinical response.

Frequently Asked Questions

Nocdurna contains desmopressin and is prescribed for central diabetes insipidus, nocturnal enuresis in children and adults, and for certain bleeding disorders such as hemophilia A and von Willebrand disease to improve clotting factor levels.

Desmopressin mimics the natural hormone vasopressin and selectively activates V2 receptors in the kidney, leading to increased water reabsorption and urine concentration. In haemostatic use, it triggers release of factor VIII and von Willebrand factor from endothelial stores.

The appropriate dose of Nocdurna is determined by the prescribing clinician based on the individual’s condition, age, renal function and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for desmopressin 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 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 (including any cold‑chain requirements) and necessary import documentation.

Nocdurna (desmopressin) is a synthetic vasopressin analogue with selective V2‑receptor activity, offering a longer half‑life and reduced vasoconstrictive (V1) effects compared with natural vasopressin. This profile provides effective antidiuretic action with a lower risk of blood‑pressure elevation.

Store Nocdurna at ambient temperature, below 25 °C, in its original packaging. Protect the tablets from moisture, direct sunlight and excessive heat to maintain potency.

Nocdurna is administered sublingually. The tablet is placed under the tongue and allowed to dissolve completely without chewing or swallowing whole, ensuring rapid absorption into the bloodstream.

The most serious risks include severe hyponatremia, which can lead to seizures or coma, and rare thrombotic events. Patients should be monitored for sudden changes in weight, headache, nausea, or neurological symptoms that may indicate low sodium levels.

Nocdurna is contraindicated in patients with known hypersensitivity to desmopressin, uncontrolled hypertension, severe renal impairment, or those at high risk for hyponatremia such as individuals with excessive fluid intake or certain endocrine disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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