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Organic Nitrate (IV) Pregnancy: Developmental toxicity studies in rats and rabbits by various routes did not reveal any effect on the embryos, fetuses or young animals even at doses toxic to the dam. Breast-feeding: available evidence is inconclusive or inadequate for determining infant risk; nitrates are excreted in breast milk and may cause methaemoglobinaemia in infants, and a risk to the suckling child cannot be excluded — decide whether to discontinue breast-feeding or the infusion, weighing the benefit of each.

Glyceryl Trinitrate (IV)

Brand names: Nitrocine, Nitronal

Intravenous glyceryl trinitrate is a fast-acting, titratable nitrate vasodilator used in hospital for unstable angina, acute heart failure with pulmonary oedema, and controlled hypotension or hypertensive emergencies.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Recommended dosage range 10-200 micrograms/min by continuous intravenous infusion, adjusted to meet the individual needs of the patient; up to 400 micrograms/min may be necessary during some surgical procedures
Route: Intravenous infusion only — administer by micro-drip set infusion pump or similar device permitting a constant infusion rate. May be given undiluted by slow IV infusion using a syringe pump with a glass or rigid plastic syringe, or as an admixture in Sodium Chloride Injection B.P. or Dextrose Injection B.P. Must NOT be given by bolus injection (§4.4)
Frequency: Continuous infusion, titrated to the desired clinical response with close haemodynamic monitoring
Max: Up to 400 micrograms/min may be necessary during some surgical procedures (highest infusion rate stated in §4.2)
Indication-specific starting rates and titration from §4.2 — Use in surgery (control of hypertension, or to produce hypotension during surgery): start 25 micrograms/min, increase by increments of 25 micrograms/min at 5-minute intervals until blood pressure is stabilised; 10-200 micrograms/min are usually sufficient during surgery, although up to 400 micrograms/min has been required in some cases. Perioperative myocardial ischaemia: start 15-20 micrograms/min, with subsequent increments of 10-15 micrograms/min until the required effect is obtained. Unresponsive congestive heart failure: start 20-25 micrograms/min; may be decreased to 10 micrograms/min, or increased in steps of 20-25 micrograms/min every 15-30 minutes until the desired effect is obtained. Unstable angina: initial 10 micrograms/min with increments of 10 micrograms/min at approximately 30-minute intervals according to the needs of the patient. Admixture example given in the SPC: to obtain 100 micrograms/mL, add 50 mL of glyceryl trinitrate solution (containing 50 mg) to 450 mL of infusion vehicle for a final volume of 500 mL; a dosage of 100 micrograms/min is then obtained by giving 60 mL of the admixture per hour. In case of dilution the product must be mixed under aseptic conditions immediately after opening; vials are single use only. Giving sets made of polyvinyl chloride (PVC) or polyurethane (PU) cause loss of active substance by adsorption — if used, the dose must be adjusted; polyethylene, polypropylene and PTFE have proven suitable. Avoid reducing systolic blood pressure below 90 mmHg. The solution contains glucose — take into account in diabetes mellitus. Tolerance and cross-tolerance to other nitro compounds has been described. Methaemoglobinaemia has been reported; methylene blue treatment is contraindicated in glucose-6-phosphate or methaemoglobin-reductase deficiency. Elderly: no evidence that a posology adjustment is required. Paediatric: safety and efficacy has not yet been established in children. Source is the UK SPC for 'Glyceryl Trinitrate 1 mg/ml solution for infusion' (eMC product 6296); §4.5 was truncated at source fetch, so the interaction list is partial and is drawn from §4.3 and §4.4. NOTE: the US label fetched as cross-check is nitroglycerin SUBLINGUAL tablets — a different route and regimen entirely; it was not used.

Dose adjustments

Renal

Additional dose adjustments in patients with severe hepatic insufficiency or severe renal failure may be necessary and require additional monitoring (§4.2); caution should be exercised in patients with severe liver or renal disease (§4.4).

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to glyceryl trinitrate, other nitrates or any of the excipients
  • Acute circulatory failure (shock, collapse); cardiogenic shock unless a sufficient end-diastolic pressure is maintained by appropriate measures; uncorrected hypovolaemia and hypotensive shock
  • Severe anaemia; arterial hypoxaemia; toxic pulmonary oedema
  • Severe cerebral haemorrhage, head trauma, and conditions associated with increased intracranial pressure
  • Constrictive pericarditis; pericardial tamponade; myocardial insufficiency due to obstruction, aortic or mitral stenosis, or hypertrophic obstructive cardiomyopathy (including angina caused by it)
  • Concurrent phosphodiesterase type 5 inhibitors (e.g. sildenafil, vardenafil, tadalafil) or the soluble guanylate cyclase stimulator riociguat

Side effects

  • Headache (very common) — dose-dependent, due to cerebral vasodilation; often regresses after a few days
  • Dizziness including postural dizziness, somnolence, asthenia (common)
  • Tachycardia (common); enhanced angina pectoris symptoms (uncommon); palpitations and increased heart rate (not known)
  • Orthostatic hypotension (common); circulatory collapse sometimes with bradyarrhythmia and syncope (uncommon); flushing and hypotension (not known)
  • Nausea and vomiting (uncommon); allergic skin reactions such as rash and allergic contact dermatitis (uncommon); injection-site pruritus, burning, erythema and irritation (uncommon)

Interactions

  • Phosphodiesterase type 5 inhibitors (sildenafil, vardenafil, tadalafil) — must not be used during nitrate therapy; they amplify the vasodilatory effect and can cause severe hypotension. Glyceryl trinitrate must not be used in patients who have taken a PDE5 inhibitor in the intervening 24 hours (48 hours for tadalafil), and patients on infusion must be warned not to take them (§4.3, §4.4)
  • Riociguat (soluble guanylate cyclase stimulator) — must not be used during nitrate therapy (§4.3)
  • Alcohol — should be avoided during treatment as it may potentiate the hypotensive and vasodilating effect (§4.4)
  • Beta-blocker — combined treatment may be used if necessary to counter a slight reflex-induced increase in heart rate (§4.8)
  • Note: eMC §4.5 itself was truncated at source fetch — the interaction list above is drawn from §4.3, §4.4 and §4.8 and is incomplete

Clinical monograph

How it works

It is metabolised to nitric oxide, which raises vascular smooth-muscle cyclic GMP to cause venous (and at higher infusion rates arterial) dilatation, reducing preload, afterload and myocardial oxygen demand.

Prescribing in practice

  • Infuse via a controlled pump with close blood-pressure monitoring because abrupt, profound hypotension can occur and the rate must be titrated to response.
  • Contraindicated with phosphodiesterase-5 inhibitors such as sildenafil owing to the risk of severe hypotension, and avoid in marked hypotension or hypovolaemia.
  • Continuous infusion leads to nitrate tolerance, and standard PVC giving sets adsorb the drug so non-absorbent infusion sets should be used.

Monitoring

Continuous blood pressure and heart rate monitoring is essential during titration, watching for hypotension, reflex tachycardia and headache.

Counselling the patient

  • Headache and flushing are common as the medicine starts working.
  • Tell staff promptly if you feel faint, dizzy or light-headed.

Evidence & guidelines

Long-established standard therapy for acute coronary and heart-failure presentations, supported by extensive clinical experience and UK guidelines.

Reference: SPC Nitronal; 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.