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Anticoagulant — VTE Prophylaxis (UFH) Pregnancy: Heparin does not cross the placenta and can be used during all trimesters if clinically needed, after risk/benefit evaluation; anticoagulant treatment of pregnant women requires specialist involvement. Reduced bone density reported with prolonged use in pregnancy. This formulation contains benzyl alcohol, which may cross the placenta and cause accumulation and toxicity (metabolic acidosis), so use of this formulation should be avoided in pregnancy. Heparin is not excreted in human milk and can be used during breast-feeding.

Heparin Unfractionated (Prophylaxis)

Brand names: Heparin Sodium (generic)

Unfractionated heparin is a parenteral anticoagulant used for venous thromboembolism prophylaxis and treatment in the surgical setting.

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: 5,000 IU
Route: Subcutaneous injection (prophylactic administration is by subcutaneous injection). Heparin must NOT be given by intramuscular injection due to the risk of haematoma.
Frequency: Patients undergoing major elective surgery: 5,000 IU 2 hours pre-operatively, then every 8-12 hours post-operatively for 10-14 days or until the patient is ambulant, whichever is the longer.
Regimen taken verbatim from the SPC (Heparin (Mucous) Injection BP 1,000 IU, section 4.2, Prophylactic Dosage): 'Patients undergoing major elective surgery: 5,000 IU should be given 2 hours pre-operatively and then every 8-12 hours post-operatively for 10-14 days or until the patient is ambulant, whichever is the longer.' Other prophylactic regimens in the same SPC: following myocardial infarction 5,000 IU twice daily for 10 days or until the patient is mobile; other patients 5,000 IU every 8-12 hours. These standard prophylactic regimens do not require routine control. TREATMENT (non-prophylaxis) doses in the same SPC: intravenous 5,000-10,000 IU every 4 hours, or 500 IU/kg bodyweight daily as a continuous infusion in sodium chloride or dextrose injection; subcutaneous initial dose 250 IU/kg bodyweight then every 12 hours - individually adjusted to maintain thrombin clotting time, whole blood clotting time or APTT 1.5 to 2 times control on blood withdrawn 4-6 hours after the first injection or start of infusion. Haemodialysis: initial bolus 1,000-5,000 IU then continuous IV infusion 1,000-2,000 IU per hour adjusted to maintain clotting time greater than 40 minutes. Pregnancy prophylaxis (this formulation contains benzyl alcohol and should be avoided in pregnancy): suggested dosage 5,000 IU every 12 hours in early pregnancy increasing to 10,000 IU every 12 hours in the last trimester, reduced during labour, with plasma heparin kept below 0.4 IU/ml by anti-Xa assay. Elderly: no dosage alteration necessary for prophylaxis. Neuraxial block timing (section 4.4): for prophylactic doses (15,000 IU/day or less) placement or removal of a peridural or spinal catheter should not be allowed until 4-6 hours after the last heparin administration and the subsequent dose not before at least 1 hour post-procedure; for treatment doses (over 15,000 IU/day) 4-6 hours after the last intravenous dose or 8-12 hours after the last subcutaneous dose. Platelet count should be measured before starting and periodically thereafter because of the risk of immune-mediated heparin-induced thrombocytopenia (type II). Children: the SPC gives only treatment guidance ('standard treatment dosages should be given initially', then individually adjusted by coagulation tests) and no paediatric weight-based prophylaxis dose - see paedDose. NOTE: the fetched SPC sections 4.4 and 4.8 were truncated at the source-fetch limit; section 4.5 was not fetched.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to the active substance or to any of the excipients
  • Current or history of immune-mediated heparin-induced thrombocytopenia (type II)
  • Active major haemorrhage and risk factors for major haemorrhage
  • Generalised or local haemorrhagic tendency, including uncontrolled severe hypertension, severe liver insufficiency, active peptic ulcer, intracranial haemorrhage or injuries and operations on the central nervous system, eyes and ears, and in women with abortus imminens (list not exhaustive)
  • Septic endocarditis
  • In patients receiving heparin for TREATMENT rather than prophylaxis: locoregional anaesthesia in elective surgical procedures, and insertion of an epidural catheter, are contraindicated (risk of epidural or spinal haematoma)
  • Contains 10 mg/ml benzyl alcohol - must not be given to premature babies or neonates due to the risk of gasping syndrome

Side effects

  • Haemorrhage (common) - may occur in any organ and at any degree of severity; haematoma (common)
  • Immune-mediated heparin-induced thrombocytopenia type II (uncommon), usually within 5-14 days of the first dose, may be associated with arterial and venous thrombosis - heparin must be discontinued in all cases; non-immune thrombocytopenia type I (uncommon)
  • Erythema (common); injection site reaction, rash, urticaria, pruritus and skin necrosis (uncommon)
  • Hyperkalaemia due to hypoaldosteronism (uncommon; rare per section 4.8 narrative) - risk in diabetes mellitus or renal impairment
  • Transaminases increased (common); APTT prolonged beyond therapeutic range (uncommon)
  • Osteoporosis with long-term treatment; anaphylactic reaction and hypersensitivity (uncommon); priapism (uncommon)

Interactions

  • Medicinal products affecting platelet function or the coagulation system - combination should be avoided or carefully monitored (SPC section 4.4; section 4.5 was not fetched)
  • Drugs affecting haemostasis (NSAIDs, platelet inhibitors, anticoagulants) increase the risk of epidural or spinal haematoma when a peridural or spinal catheter is used (SPC section 4.4)

Clinical monograph

How it works

It potentiates antithrombin, accelerating inactivation of thrombin (factor IIa) and factor Xa, thereby inhibiting clot formation.

Prescribing in practice

  • Bleeding is the main risk; assess bleeding risk against thrombotic risk and remember protamine is available for reversal.
  • Heparin-induced thrombocytopenia is an important immune-mediated complication; monitor platelets and stop if suspected.
  • It has a short half-life, making it useful where rapid offset or reversibility is desirable, such as around surgery.

Monitoring

Monitor for bleeding and platelet count, with APTT monitoring used when given at treatment (rather than prophylactic) intensity.

Counselling the patient

  • Report unusual bruising, bleeding or black stools promptly.
  • Tell the team about any history of low platelets or reaction to heparin.

Evidence & guidelines

NICE guidance on venous thromboembolism (NG89) supports pharmacological prophylaxis in surgical patients after individual risk assessment.

Reference: ASRA Guidelines; NICE NG89; BCSH Heparin Guidelines; 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.