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Haemostasis Pregnancy: NOT AVAILABLE FROM THE UK SPC — the eMC bundle for Octim Injection contains no §4.6, so no UK pregnancy or lactation wording could be sourced. CROSS-CHECK, US PROVENANCE ONLY (oral tablet label for diabetes insipidus/nocturnal enuresis, a different product and route): 'Pregnancy Category B... There are, however, no adequate and well-controlled studies in pregnant women. Because animal studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. Several publications where desmopressin acetate was used in the management of diabetes insipidus during pregnancy are available; these include a few anecdotal reports of congenital anomalies and low birth weight babies. However, no causal connection between these events and desmopressin acetate has been established. A fifteen year Swedish epidemiologic study of the use of desmopressin acetate in pregnant women with diabetes insipidus found the rate of birth defects to be no greater than that in the general population; however, the statistical power of this study is low. As opposed to preparations containing natural hormones, desmopressin acetate in antidiuretic doses has no uterotonic action and the physician will have to weigh the possible therapeutic advantages against the possible risks in each case.' No breastfeeding statement was fetched from either label.

Desmopressin

Brand names: DDAVP, Octim, Stimate

Desmopressin is a synthetic analogue of vasopressin (antidiuretic hormone) used for cranial diabetes insipidus and nocturnal enuresis, and to transiently raise factor VIII and von Willebrand factor in mild haemophilia A and von Willebrand disease.

Adult dose

Dose: 0.3 micrograms per kilogram body weight
Route: By subcutaneous injection or intravenous infusion. §4.2, verbatim: 'For intravenous infusion, the dose should be diluted in 50ml of 0.9% sodium chloride for injection and given over 20 minutes.'
Frequency: Given immediately prior to surgery or following trauma. §4.2, verbatim: 'Further doses may be administered at 12 hourly intervals so long as cover is required.'
SCOPE: this covers the page's primary indication and primary route — haemostatic cover, given SC or IV. The INTRANASAL route the page also lists is NOT covered: the product fetched is Octim Injection, and no nasal-spray posology appears anywhere in this bundle, so the page's intranasal figures have not been re-sourced. || §4.2 MILD TO MODERATE HAEMOPHILIA AND VON WILLEBRAND'S DISEASE, verbatim: 'By subcutaneous or intravenous administration. The dose for adults, children and infants is 0.3 micrograms per kilogram body weight, administered by subcutaneous injection or intravenous infusion. Further doses may be administered at 12 hourly intervals so long as cover is required. As some patients have shown a diminishing response to successive doses, it is recommended that monitoring of Factor VIII levels should continue. For intravenous infusion, the dose should be diluted in 50ml of 0.9% sodium chloride for injection and given over 20 minutes. This dose should be given immediately prior to surgery or following trauma.' || EXPECTED RESPONSE, §4.2: 'Increase of Factor VIII levels are dependent on basal levels and are normally between 2 and 5 times the pre-treatment levels. If results from a previous administration of desmopressin are not available then blood should be taken pre-dose and 20 minutes post-dose for assay of Factor VIII levels in order to monitor response.' || SURGERY, §4.2: 'Unless contraindicated, when surgery is undertaken tranexamic acid may be given orally at the recommended dose from 24 hours beforehand until healing is complete.' || A SECOND, DIFFERENT USE IN THE SAME §4.2 — FIBRINOLYTIC RESPONSE TESTING (a diagnostic test, not haemostatic cover): 'The dose for adults and children is 0.3 micrograms per kilogram body weight, administered by subcutaneous injection or intravenous infusion... A sample of venous blood should be taken 20 minutes after the administration. In patients with a normal response the sample should show fibrinolytic activity of euglobulin clot precipitate on fibrin plates of at least 240mm2.' Note §4.3 bars this test in hypertension, heart disease, cardiac insufficiency and conditions requiring diuretics. || NO MAXIMUM DOSE IS STATED ANYWHERE IN THIS SPC, so maxDose is empty. || ADMINISTRATION EFFECT, §4.2: 'During administration of intravenous desmopressin, vasodilation may occur resulting in decreased blood pressure and tachycardia with facial flushing in some patients.' §4.8 adds this 'is normally avoided by infusing the product over 20 minutes'.

Paediatric dose

Dose: 0.3 micrograms/kg
Route: By subcutaneous injection or intravenous infusion; for intravenous infusion, diluted in 50 ml of 0.9% sodium chloride for injection and given over 20 minutes
Frequency: Given immediately prior to surgery or following trauma; further doses may be administered at 12 hourly intervals so long as cover is required
THE SAME PER-DOSE FIGURE APPLIES ACROSS THE WHOLE PAEDIATRIC RANGE — §4.2, verbatim: 'The dose for adults, children and infants is 0.3 micrograms per kilogram body weight, administered by subcutaneous injection or intravenous infusion.' The SPC states one weight-based per-dose figure for adults, children and infants alike, with no age band, no weight band and no separate paediatric ceiling, which is why dosePerKg carries it. || NO MAXIMUM DOSE IS STATED, so maxDose is empty and the calculator applies no cap. || NO LOWER AGE OR WEIGHT CUT-OFF APPEARS IN ANY FETCHED SECTION of this SPC — the absence of one here is not evidence that none exists. || CONCENTRATION IS NULL: the strength of Octim Injection is not stated in any fetched section, so no mg/mL figure could be sourced and no volume can be derived here — read the strength off the ampoule. || FLUID RESTRICTION IS MANDATORY AROUND THE DOSE, §4.4 verbatim: 'When repeated doses are used to control bleeding in haemophilia or von Willebrand's disease, care should be taken to prevent fluid overload. Fluid should not be forced, orally or parenterally, and patients should only take as much fluid as they require to satisfy thirst. Intravenous infusions should not be left up as a routine after surgery.' || §4.8 records a paediatric-specific signal: 'Very rare cases of emotional disorders including aggression in children have been reported.' || Verify all under-18 dosing against a children's formulary before prescribing.

Dose adjustments

Renal

No numeric renal dose adjustment is stated in the UK SPC. §4.4, verbatim: 'Care should be taken with patients who have reduced renal function and/or cardiovascular disease.' CROSS-CHECK, US PROVENANCE — the US oral tablet label goes further and makes renal impairment an outright bar: 'Desmopressin acetate tablets are contraindicated in patients with moderate to severe renal impairment (defined as a creatinine clearance below 50mL/min).' That statement belongs to a different product, route and indication (oral tablets for diabetes insipidus/nocturnal enuresis) and is recorded here as a flag, not as a rule for the parenteral haemostatic dose above.

Hepatic

No hepatic impairment dose adjustment, and no hepatic caution of any kind, is stated in any fetched section of this SPC or of the US label.

Dose independently re-sourced from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — clinician-reviewed. Always confirm against the product SmPC and your local formulary before prescribing.

Paediatric weight-based calculator

THE SAME PER-DOSE FIGURE APPLIES ACROSS THE WHOLE PAEDIATRIC RANGE — §4.2, verbatim: 'The dose for adults, children and infants is 0.3 micrograms per kilogram body weight, administered by subcutaneous injection or intravenous infusion.' The SPC states one weight-based per-dose figure for adults, children and infants alike, with no age band, no weight band and no separate paediatric ceiling, which is why dosePerKg carries it. || NO MAXIMUM DOSE IS STATED, so maxDose is empty and the calculator applies no cap. || NO LOWER AGE OR WEIGHT CUT-OFF APPEARS IN ANY FETCHED SECTION of this SPC — the absence of one here is not evidence that none exists. || CONCENTRATION IS NULL: the strength of Octim Injection is not stated in any fetched section, so no mg/mL figure could be sourced and no volume can be derived here — read the strength off the ampoule. || FLUID RESTRICTION IS MANDATORY AROUND THE DOSE, §4.4 verbatim: 'When repeated doses are used to control bleeding in haemophilia or von Willebrand's disease, care should be taken to prevent fluid overload. Fluid should not be forced, orally or parenterally, and patients should only take as much fluid as they require to satisfy thirst. Intravenous infusions should not be left up as a routine after surgery.' || §4.8 records a paediatric-specific signal: 'Very rare cases of emotional disorders including aggression in children have been reported.' || Verify all under-18 dosing against a children's formulary before prescribing.

Verify in a children's formulary

US labelling (FDA)

Reference — US labelling, may differ from UK

DOSAGE AND ADMINISTRATION Central Diabetes Insipidus The dosage of desmopressin acetate tablets must be determined for each individual patient and adjusted according to the diurnal pattern of response. Response should be estimated by two parameters: adequate duration of sleep and adequate, not excessive, water turnover. Patients previously on intranasal desmopressin acetate therapy should begin tablet therapy twelve hours after the last intranasal dose. During the initial dose titration period, patients should be observed closely and appropriate safety parameters measured to assure adequate response. Patients should be monitored at regular intervals during the course of desmopressin acetate …

Source: US FDA prescribing information (openFDA / DailyMed), label dated 2025-11-13. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.

Contraindications

  • §4.3, verbatim — 'OCTIM Injection is contraindicated in cases of: habitual and psychogenic polydipsia'
  • Unstable angina pectoris (§4.3)
  • Decompensated cardiac insufficiency (§4.3)
  • von Willebrand's Disease Type IIB — §4.3, verbatim: 'where the administration of desmopressin may result in pseudothrombocytopenia due to the release of abnormal clotting factors which cause platelet aggregation'
  • Applies to the diagnostic use only — §4.3, verbatim: 'Fibrinolytic Response Testing should not be carried out in patients with hypertension, heart disease, cardiac insufficiency and other conditions requiring treatment with diuretic agents.'
  • NOT a contraindication but a §4.4 precaution — measures to prevent fluid overload must be taken in 'conditions characterised by fluid and/or electrolyte imbalance', in 'patients at risk for increased intracranial pressure', and in 'patients with conditions requiring treatment with diuretic agents'
  • NOT a contraindication but a §4.4 limitation of effect — 'OCTIM Injection does not reduce prolonged bleeding time in thrombocytopenia.'
  • CROSS-CHECK, US PROVENANCE (oral tablet label, different route and indication) — contraindicated in known hypersensitivity to desmopressin acetate or any component, in moderate to severe renal impairment (creatinine clearance below 50 mL/min), and 'in patients with hyponatremia or a history of hyponatremia'

Side effects

  • §4.8, verbatim: 'Side-effects include headache, stomach pain and nausea.'
  • §4.8: 'Isolated cases of allergic skin reactions and more severe general allergic reactions have been reported.'
  • §4.8: 'Very rare cases of emotional disorders including aggression in children have been reported.'
  • Water retention / hyponatraemia — the dose-limiting harm; §4.8, verbatim: 'Treatment with desmopressin without concomitant reduction of fluid intake may lead to water retention/hyponatraemia with accompanying symptoms of headache, nausea, vomiting, weight gain, decreased serum sodium and in serious cases, convulsions.'
  • §4.8: 'During intravenous infusion of OCTIM Injection, vasodilation may occur, resulting in decreased blood pressure and tachycardia with facial flushing. This side effect is normally avoided by infusing the product over 20 minutes.'
  • CROSS-CHECK, US PROVENANCE (oral/intranasal label): large doses of the intranasal formulations 'have produced transient headache, nausea, flushing and mild abdominal cramps... These symptoms have disappeared with reduction in dosage'; transient increases in AST no higher than 1.5 times the upper limit of normal in long-term diabetes insipidus use; and 'rare reports of hyponatremic convulsions associated with concomitant use with the following medications: oxybutinin and imipramine'

Monitoring

  • Factor VIII levels — §4.2: 'As some patients have shown a diminishing response to successive doses, it is recommended that monitoring of Factor VIII levels should continue.' If no prior response data exist, 'blood should be taken pre-dose and 20 minutes post-dose for assay of Factor VIII levels in order to monitor response'; expect a rise to 2-5 times pre-treatment levels
  • Fluid balance and thirst-limited intake — §4.4: fluid must not be forced orally or parenterally, and IV infusions 'should not be left up as a routine after surgery'
  • Body weight, plasma sodium and plasma osmolality — §4.4: 'Fluid accumulation can be readily monitored by weighing the patient or by determining plasma sodium or osmolality.'
  • STOP RULE, §4.4 verbatim: 'If there is a gradual increase of the body weight, decrease of serum sodium to below 130mmol/l or plasma osmolality to below 270mOsm/kg, the fluid intake must be reduced drastically and the administration of OCTIM Injection interrupted.'
  • Blood pressure — §4.4: 'During administration of OCTIM Injection, it is recommended that the patient's blood pressure is monitored continuously'; watch also for tachycardia and facial flushing from vasodilation (§4.2/§4.8)
  • Review co-prescriptions that add antidiuretic effect — §4.5: tricyclic antidepressants, SSRIs, chlorpromazine and carbamazepine 'may cause an additive antidiuretic effect leading to an increased risk of water retention and/or hyponatraemia', and 'NSAIDs may induce water retention and/or hyponatraemia'
  • For the diagnostic use, take the venous sample 20 minutes after administration (§4.2)

Clinical monograph

How it works

It acts on renal vasopressin (V2) receptors to promote water reabsorption, and stimulates release of factor VIII and von Willebrand factor from endothelial stores, briefly improving haemostasis.

Prescribing in practice

  • Hyponatraemia from water retention is the key hazard and can cause seizures, so fluid restriction and sodium monitoring around dosing are essential.
  • Use with caution where fluid overload is a concern, including cardiac or renal impairment, and in older people who are more susceptible to water intoxication.
  • Effectiveness in raising clotting factors diminishes with repeated doses (tachyphylaxis), limiting its use over consecutive days for haemostatic indications.

Monitoring

Monitor serum sodium and fluid balance, especially at initiation and when the indication carries a high water-retention risk; for haemostatic use assess factor VIII or von Willebrand factor response and clinical bleeding.

Counselling the patient

  • Follow the fluid-restriction advice given, and report headache, nausea, drowsiness or confusion, which may signal low sodium.
  • Seek urgent help if a seizure or marked drowsiness occurs.
  • For bedwetting, avoid drinking large amounts of fluid in the evening as advised.

Evidence & guidelines

A standard treatment for cranial diabetes insipidus and a recognised option in nocturnal enuresis and in mild haemophilia A and von Willebrand disease.

Reference: UKHCDO Guidelines for vWD; MHRA DSU 2017 (hyponatraemia); BSH Guidelines on haemophilia; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.

📚 MRCEM Revision

Featured in these MRCEM clinical pathways

Desmopressin is a core drug in the following exam-focused workups on our sister siteReviseMRCEM.

MRCEM Primary / Intermediate / OSCE candidates: each pathway includes exam-style questions, RCEM/NICE citations, and FAQ summaries.