Registered Zambia · ZAMRA

PARIN-E

Enoxaprin Sodium 60mg/0.6 ml mg/ml

ZAMRA-HM-26-162 Liquid 60mg/0.6 ml mg/ml

What it does

Enoxaparin is a medication that helps prevent and treat blood clots.

Commonly used for: prevention of blood clots after surgery, treatment of deep vein thrombosis (DVT), treatment of pulmonary embolism (PE), prevention of blood clots in patients with certain heart conditions

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Registration & product details

Registration no.
ZAMRA-HM-26-162
Registration date
2026-04-21
Expiry date
2031-04-20
Status
Registered/Compliant
Active ingredient
Enoxaprin Sodium 60mg/0.6 ml mg/ml
Dosage form
Liquid
Strength
60mg/0.6 ml mg/ml
Pack size
-
Therapeutic class
-
Manufacturer / MAH
Venus Remedies
Applicant / LTR
Venus Remedies Limited
Country of origin
India
Manufacturer location
Jharmajri EPIP, Phase- I, Extension Bhatoli Kalan, Barotiwala, Baddi, Himachal Pradesh 174103, India

Source: Zambia Medicines Regulatory Authority · fetched 2026-04-24 14:14:10 · updated 2026-09-24 03:38:59

Disclaimer: This information is sourced from Zambia Medicines Regulatory Authority (Zambia). Always consult a qualified healthcare professional before using any medication.

About this medicine

Enoxaparin is a medication that helps prevent and treat blood clots.

What it treats

  • prevention of blood clots after surgery
  • treatment of deep vein thrombosis (DVT)
  • treatment of pulmonary embolism (PE)
  • prevention of blood clots in patients with certain heart conditions

How it works

It works by thinning the blood, making it less likely to form clots.

Who it's for

This medication is for adults who need help preventing or treating blood clots.

Cautions

  • • Do not use if you have a history of severe allergic reactions to similar medications.
  • • Use with caution if you have bleeding disorders or severe kidney problems.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: enoxaprin

Enoxaparin is a low molecular weight heparin (LMWH) used primarily as an anticoagulant. It is derived from unfractionated heparin and is employed to prevent and treat thromboembolic disorders. Enoxaparin is commonly used in the management of conditions such as deep vein thrombosis (DVT), pulmonary embolism (PE), and in patients undergoing certain types of surgery to reduce the risk of venous thromboembolism.

Indications

  • Prophylaxis of deep vein thrombosis (DVT) in patients undergoing surgery
  • Treatment of DVT and pulmonary embolism (PE)
  • Prevention of thromboembolic complications in patients with unstable angina or non-ST elevation myocardial infarction (NSTEMI)
  • Management of acute ST elevation myocardial infarction (STEMI) in conjunction with percutaneous coronary intervention
  • Prevention of thrombus formation in patients with certain medical conditions

Dosage

Children: Refer to the BNF for Children for

Adults: Refer to the BNF for specific dosing guidelines based on the indication and patient factors.

Mechanism of action

Enoxaparin exerts its anticoagulant effect by inhibiting factor Xa and, to a lesser extent, factor IIa (thrombin) in the coagulation cascade. It enhances the activity of antithrombin III, which inhibits the conversion of prothrombin to thrombin and the conversion of fibrinogen to fibrin, thereby preventing clot formation.

Pharmacodynamics

The pharmacodynamic effects of enoxaparin include dose-dependent anticoagulation, which is monitored through anti-factor Xa levels. The drug has a predictable pharmacokinetic profile, allowing for fixed dosing without routine coagulation monitoring in most patients. Enoxaparin's effects are prolonged compared to unfractionated heparin, and it has a lower risk of inducing thrombocytopenia.

Pharmacokinetics

Enoxaparin is administered subcutaneously and is well absorbed, with peak plasma concentrations occurring approximately 3 to 5 hours after administration. It has a bioavailability of approximately 90%, and its elimination half-life is around 4 to 5 hours. The drug is primarily eliminated by renal excretion, necessitating dose adjustments in patients with renal impairment.

Contra-indications

  • Active major bleeding
  • Severe thrombocytopenia
  • Hypersensitivity to enoxaparin or any component of the formulation
  • History of heparin-induced thrombocytopenia
  • Active ulcer disease

Adverse effects

  • Bleeding
  • Thrombocytopenia
  • Injection site reactions
  • Allergic reactions
  • Liver enzyme elevation
  • Osteoporosis (with long-term use)
  • Anemia

Interactions

  • Other anticoagulants (may increase bleeding risk)
  • Non-steroidal anti-inflammatory drugs (NSAIDs) (may increase risk of gastrointestinal bleeding)
  • Antiplatelet agents (e.g., aspirin, clopidogrel) (increased risk of bleeding)
  • Certain herbal supplements (e.g., ginkgo biloba, garlic) (may increase bleeding risk)

Precautions

  • Use with caution in patients with renal impairment
  • Monitor patients with a history of bleeding disorders
  • Regular monitoring of platelet counts is recommended
  • Use during and after procedures that may increase bleeding risk

Pregnancy

Enoxaparin is classified as category B. It may be used in pregnancy if the benefits outweigh the risks, particularly in patients with a history of thromboembolic events.

Breast-feeding

Enoxaparin is excreted in breast milk in small amounts. Caution is advised, but it is generally considered compatible with breastfeeding.

Storage

Store at room temperature (15-30°C), protect from light. Do not freeze.

Formulations

  • Enoxaparin sodium injection (pre-filled syringes)
  • Enoxaparin sodium vial for injection

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.