Clexane Duo

Quick links to important sections

Medically reviewed

Laura Arias

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Clexane Duo

Clexane Duo is a prescription-only pharmaceutical preparation that serves as an anticoagulant, commonly referred to as a blood thinner. Its primary function is to prevent the formation of inappropriate blood clots within the body, a process known as antithrombotic prophylaxis.


Quick Facts

Property Description
Active ingredient Enoxaparin Sodium
Form Sterile solution for injection (pre-filled syringe)
Pharmacological class Low Molecular Weight Heparin (LMWH), Antithrombotic agent
Common use Prevention and management of blood clots (thromboembolism)
Origin Semi-synthetic, derived from porcine intestinal mucosa
Manufacturer (Originator) Sanofi Winthrop Industrie (France)

Identity and Pharmacological Classification

Clexane Duo contains the active ingredient Enoxaparin Sodium, which is classified within the Low Molecular Weight Heparin (LMWH) group of anticoagulants. As an LMWH, it exhibits a selective action profile, primarily targeting a specific enzyme in the clotting process, Factor Xa. This agent belongs to the Heparin group (ATC B01AB05), confirming its role in managing blood coagulation. Clexane Duo is the brand name for this formulation, originally developed by Sanofi Winthrop Industrie, a factor that establishes its originator status for the Enoxaparin molecule.

Composition, Form, and Biological Origin

The active substance, Enoxaparin Sodium, is a complex semi-synthetic derivative of natural Heparin. Its origins are biological, as it is chemically derived from porcine intestinal mucosa and further processed to yield smaller molecular fragments. This medicine is supplied as a sterile solution for injection, typically packaged in a pre-filled syringe with Water for Injection as the aqueous base. Its concentration is standardized and measured in anti-Xa International Units (anti-Xa IU), reflecting its specific functional potency against Factor Xa.

General Purpose of this Anticoagulant Type

The general protective purpose of this medication is to provide antithrombotic prophylaxis, maintaining the fluidity of blood flow to prevent thrombi (blood clots). Enoxaparin is an effective form of prophylaxis for thromboembolic disease in patients deemed to be at moderate to high risk. This indicates that the medicine is instrumental in providing a critical safeguard against dangerous clot formation, such as in typical use scenarios like prolonged immobility following surgery.

Regulatory References

  1. European Medicines Agency (EMA) on Enoxaparin
  2. Inhixa (Enoxaparin Sodium) EPAR
  3. Enoxaparin - StatPearls (NIH Bookshelf)

What side effects are possible with Clexane Duo?

Possible Side Effects and Safety Information

This section describes the officially documented adverse reactions and safety characteristics of Enoxaparin Sodium (Clexane Duo), as defined by government regulatory documents, focusing strictly on safety data and frequency classifications.


Frequency-Classified Adverse Reactions

The primary safety characteristic is the risk of Hemorrhage (Bleeding), which is formally classified as a Very Common event (affecting 1 in 10 patients) in official prescribing information. Other commonly documented effects include:

  • Common (1 in 100 to <1 in 10): Thrombocytopenia (low platelet count), increases in serum aminotransferases (liver enzymes), and injection site reactions (e.g., pain, bruising).
  • Uncommon and Rare: Less frequent documented reactions include urticaria (hives) and, rarely, severe systemic reactions like anaphylaxis.

System-Organ Class and Serious Reactions

Adverse effects are categorized by the physiological systems they affect. Regulatory documents note risks within the Blood and Lymphatic System Disorders (e.g., hemorrhage, thrombocytopenia) and the Hepatobiliary Disorders (enzyme elevations).

Serious Adverse Reactions specifically highlighted in official labeling include Major Hemorrhage (such as intracranial bleeding) and the potential for a Spinal or Epidural Hematoma following neuraxial procedures (a rare but serious risk of neurological injury).


Population and Exposure-Related Safety

Official documents outline specific safety considerations for certain patient groups. An increased risk of bleeding is noted for older adults (especially those over 80 years) and individuals with severe renal impairment, due to altered drug clearance. Furthermore, Osteoporosis is documented as an adverse effect associated only with long-term therapy. Use is formally restricted by official contraindications, including the presence of active major bleeding or a history of Heparin-Induced Thrombocytopenia (HIT).

Overdose and Emergency Response

Overdose and When to Seek Help

Official regulatory information for Clexane Duo (Enoxaparin Sodium) focuses on the manifestation of an exaggerated anticoagulant effect and the required emergency response actions.

Documented Overdose Manifestations

The principal outcome of an overdose is excessive bleeding or severe hemorrhage. Documented signs of heightened anticoagulant effect include black or tarry stools, nosebleeds, bleeding gums, and easy bruising. In severe cases, the effect can impact the neurological system, presenting a risk of spinal or epidural hematomas.

Emergency Actions and Support

Element Official Guidance
When to Seek Help Seek immediate emergency medical attention or call the Poison Help line upon suspecting an overdose or observing signs of severe bleeding.
Antidote Protamine sulfate is documented for the partial reversal of the anticoagulant activity, neutralizing approximately 60% of the anti-Factor Xa effect.
Support Management requires symptomatic and supportive treatment alongside close clinical and laboratory monitoring.

Population-Specific Overdose Considerations

Patients with severe renal impairment (kidney problems) are specifically noted in regulatory documentation as being at increased risk for drug accumulation, which can lead to overdose manifestations.

Therapeutic Uses of Clexane Duo

What Clexane Duo Treats: Main Uses and Benefits

Clexane Duo is relevant for easing symptoms related to systemic imbalance and is commonly used across conditions presenting with acute episodes related to blood clot formation. It is applied across domains where additional symptomatic support is needed.

Core Therapeutic Domains

This medication is relevant in clinical settings marked by increased discomfort or tension to address symptom clusters that may become intense or disruptive. The medication is commonly used across conditions presenting with acute episodes, including situations involving systemic discomfort. It supports patients during difficult episodes by easing distress and contributes to easing the overall symptom load.

The treatment is relevant for easing symptoms when supportive symptom management is appropriate. It is considered relevant in contexts involving heightened systemic burden. This benefit is relevant during challenging symptomatic phases, such as recovery after major procedures or periods of increased physiological stress. It may assist with maintaining functional stability and supports patients during episodes of heightened discomfort.

Providing Supportive Relief

Clexane Duo is generally used when short-term symptomatic assistance is needed in situations involving certain distressing symptoms. It is applied in scenarios where additional management of discomfort is required in high-risk settings.


Quick Fact: Supports management of symptoms that create noticeable physiological strain

Regulatory References

  1. NIH DailyMed official label for Enoxaparin Sodium Injection

Eligibility and Restrictions for Use

Clexane Duo (Enoxaparin Sodium) eligibility is strictly defined by regulatory authorities based on a patient's clinical status and specific physiological characteristics. Its use is contraindicated in patients experiencing active major bleeding, those with a history of Heparin-Induced Thrombocytopenia (HIT), or with a known hypersensitivity to enoxaparin, heparin, or pork products.

Population Status Regulatory Rule
Contraindicated Conditions Active major bleeding, Hemorrhagic stroke, Active gastric or duodenal ulceration.
Severe Restriction Severe Renal Impairment (CrCl < 30 mL/min) requires dose adjustment due to drug accumulation.
Use Not Established Pediatric population (children and adolescents).
Conditional Use Older adults (ge 75 years) and low-weight patients must be monitored for increased bleeding risk.
Pregnancy Generally permitted, but is specifically not recommended for pregnant women with mechanical prosthetic heart valves due to increased risk of thrombosis.

The medicine is permitted for use in the general adult population for all labeled indications. Use in the multi-dose formulation is contraindicated in premature neonates due to the presence of benzyl alcohol.

What should I know about interactions with other medicines?

Clexane Duo's interaction profile is primarily defined by the risk of additive hemorrhage and strict procedural timing constraints, according to regulatory documentation.

Documented Interaction Classes

Classification Interacting Agents or Conditions
Pharmacodynamic Risk Antiplatelet agents (e.g., Aspirin, Clopidogrel), Non-Steroidal Anti-Inflammatory Drugs (NSAIDs), Oral Anticoagulants, and Thrombolytic agents.
Exposure Modification Severe Renal Impairment (CrCl < 30 mL/min), which leads to increased systemic exposure.
Contraindicated Exchange Unfractionated Heparin and other Low Molecular Weight Heparins (LMWHs).

Official Interaction Constraints

Regulatory authorities mandate specific restrictions for use with other products. Co-administration with other blood thinners or antiplatelet agents may cause a pharmacodynamic interaction that increases the risk of bleeding. Alcohol consumption is also associated with an increased risk of hemorrhagic complications.

Furthermore, strict timing-based interaction rules apply to neuraxial procedures (spinal/epidural anesthesia or puncture). The drug must be separated from needle or catheter placement/removal by at least 12 hours for lower doses or 24 hours for higher doses. Subsequent post-procedure doses must be administered no sooner than 4 hours after catheter removal.

The official profile also notes that Severe Renal Impairment is a factor that significantly alters exposure, necessitating a dedicated approach due to reduced clearance.

Mechanism of Action

Targeted Acceleration of Antithrombin Activity

Clexane Duo (Enoxaparin Sodium) initiates its mechanism by binding to Antithrombin (AT), a naturally occurring plasma protein. This binding acts as a catalytic cofactor, accelerating the rate at which Antithrombin performs its inhibitory activity. This molecular interaction fundamentally promotes the systemic modulation of the coagulation cascade by increasing the speed of inhibition, which restricts the window of opportunity for pro-clotting enzymes to propagate.


Selective Inhibition of Factor Xa (FXa)

The direct consequence of the Antithrombin-drug complex formation is the significant, selective inhibition of Coagulation Factor Xa. By blocking this critical enzyme at the start of the common pathway, the drug prevents the efficient conversion of Prothrombin into Thrombin (Factor IIa). This suppression of Thrombin generation is the key physiological action that results in an overall antithrombotic state.


Mechanism Selectivity and Constraint

As a Low Molecular Weight Heparin (LMWH), the drug's physical size constrains its ability to inhibit Factor IIa (Thrombin) directly, favoring FXa inhibition by a ratio of approximately 3:1 or 4:1. This selectivity defines its mechanism, which primarily acts by rate-limiting the upstream cascade.

Dosage and Administration Information

Official Administration Principles

Clexane Duo (Enoxaparin Sodium) is administered primarily by deep subcutaneous (SC) injection for most treatment and prophylactic regimens. A specific administration protocol is required: the injection must be given into the anterolateral or posterolateral abdominal wall, with the site alternated between the left and right sides. During SC administration, the air bubble present in the pre-filled syringe is intentionally not expelled to avoid the loss of medication. The use of an intravenous (IV) bolus is officially restricted to the initial phase of treatment for acute ST-segment Elevation Myocardial Infarction (STEMI).

Standard Dosing and Frequency

Established protocols define dosing based on the clinical context. For prophylaxis (prevention), a common regimen is a fixed dose of 40 mg SC once daily. For the treatment of conditions like deep vein thrombosis, dosing is weight-based, such as 1 mg/kg SC every 12 hours. Prophylactic courses are typically of a short duration, lasting seven to ten days, though extended prophylaxis for up to three weeks is specified following certain orthopedic procedures. When a once-daily dose is missed, standard practice involves skipping the missed dose and resuming the normal schedule on the next day, rather than doubling the dose.

Population-Specific Use Constraints

Dosage modification is required for certain patient groups. For patients with severe renal impairment (creatinine clearance 15–30 mL/min), a reduction in dose and/or frequency is necessary for both prophylaxis and treatment. Similarly, in the acute STEMI setting, patients over 75 years of age do not receive the initial IV bolus, and the subsequent SC maintenance dose is reduced to 0.75 mg/kg every 12 hours.

Recent Clinical Evidence

Research evidence / Overview of studies for Clexane Duo

Research Evidence for Preventing Blood Clots After Major Procedures

Research has been conducted in the form of large Randomized Controlled Trials (RCTs) and cohort studies to explore the use of this medicine in studies examining outcomes related to blood clot formation, known as venous thromboembolism (VTE), following certain surgical procedures. Studies specifically explored the patterns observed in patients evaluated with the medicine after major orthopedic operations, such as hip or knee replacement, as well as following general abdominal or pelvic surgery, including procedures for cancer. These trials focused on outcomes related to physical discomfort and systemic or functional imbalance by measuring the incidence of blood clots (DVT or PE) that were confirmed through medical imaging, and also monitored rates of major hemorrhage.

Research Evidence for Managing Acute Illness and Restricted Mobility

This block outlines the design of the pivotal Randomized Controlled Trials that was evaluated in adult medical patients who had severely restricted mobility during an acute illness. These studies explored whether the use of the medicine was observed in some studies to have different rates of VTE events and monitored survival outcomes over defined time intervals. A key limitation is that research focusing on dosing strategies reported that findings were mixed in certain high-risk subgroups, particularly in critically ill patients, where research suggests measured anti-Xa levels were highly variable. Therefore, the certainty remains low regarding outcomes related to the generalized use of standard dosing, and data are still emerging to address these issues.

Research Evidence for Treating Existing Clots and Acute Heart Conditions

Research describes that the medicine was evaluated in studies for the treatment of acute, existing blood clots (DVT and PE), and was evaluated in patients presenting with acute coronary syndromes, such as unstable angina and Non-ST-Elevation Myocardial Infarction (NSTEMI). For the treatment of existing clots, meta-analyses and trials compared this medicine to older standard treatments, with research examining outcomes related to clot recurrence and monitoring physiological strain related to bleeding. Studies also explored outcomes related to the use of this medicine alongside specific combination therapies.

Key Studies & References

  1. Enoxaparin is superior to unfractionated heparin for preventing clinical events at 1-year follow-up of TIMI 11B and ESSENCE (Acute Coronary Syndrome Meta-Analysis)
  2. Low-Molecular-Weight Heparin (LMWH) - StatPearls - NCBI Bookshelf (Review of PK/PD and dosing in special populations)

Frequently Asked Questions (FAQ)

Common questions about Clexane Duo (FAQ)


Q: What is the main difference between Clexane Duo and regular Clexane (enoxaparin)?

Both products contain the same active ingredient, enoxaparin sodium. Official documentation states that different brands or devices may have variations in the injection technique and delivery system.

Official documents often note that different enoxaparin brands may have non-interchangeable injection devices, which is a key consideration when switching products.


Q: Does Clexane Duo thin the blood, and how is it different from aspirin?

Yes, Clexane Duo is classified as an anticoagulant, meaning it is a blood thinner. It works by targeting specific proteins in the clotting cascade, such as Factor Xa.

Aspirin is a different type of medicine called an antiplatelet agent, which affects how blood cells called platelets stick together. Because they affect the blood in different ways, regulatory sources indicate that their combined use may lead to an increased risk of bleeding complications.


Q: Why do people who are traveling long distances sometimes need Clexane Duo?

Official information indicates this medicine is used for the prevention of blood clots (VTE) in patients with significantly restricted mobility.

Periods of prolonged sitting or inactivity, such as during long travel, are recognized as a risk factor for forming blood clots in the legs. For high-risk individuals, prophylaxis is a recognized strategy to address the risk associated with such reduced movement.


Q: Can Clexane Duo be taken with common over-the-counter pain relievers?

Regulatory documents warn that using this medication with Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) may increase the risk of bleeding.

Many common over-the-counter pain relievers, such as ibuprofen and naproxen, belong to the NSAID class. Regulatory documents strongly suggest reviewing the product label for all concurrent medications to understand the potential risk of interaction.


Q: How quickly does Clexane Duo start to work after the first injection?

After a subcutaneous injection (under the skin), the medicine's anti-clotting activity in the blood is typically at its highest level within three to five hours.

This peak anti-Factor Xa activity serves as a measure of when the medicine’s maximum effect is reached.


Q: Does Clexane Duo stay in your system for a long time?

No, it is considered a short-acting anticoagulant. Official pharmacokinetic data indicates that the medicine has an elimination half-life of about four hours after a single dose, which may extend to about seven hours with repeated use.

Due to this short duration, the anti-clotting effect is cleared from the body relatively quickly.


Q: Are there any major food or drink restrictions while using Clexane Duo?

Regulatory documents specifically warn that alcohol consumption is associated with an increased risk of hemorrhagic complications.

The official prescribing information generally does not list major food restrictions.


Q: Why does Clexane Duo need to be injected and not taken as a pill?

The medicine must be given by injection because its molecular structure means it has very low oral bioavailability.

This is a term meaning the active ingredient is not effectively absorbed when taken by mouth. The medicine is administered by injection because the active ingredient is not effectively absorbed when taken orally.


Q: Is Clexane Duo considered a high-risk medication during pregnancy?

Regulatory guidance states that the drug is generally permitted for use during pregnancy when the clinical benefit to the mother outweighs the potential risks.

However, it is specifically not recommended for pregnant women who have mechanical prosthetic heart valves due to concerns about thrombosis.


Q: Can older adults or elderly people use Clexane Duo safely?

Use in older adults is permitted, but official prescribing information notes an increased risk of bleeding, particularly in individuals over 80 years of age.

For some indications, a dose adjustment may be necessary for patients aged 75 and older. Official guidelines state that this population may be subject to additional monitoring.


Q: Is Clexane Duo the same drug as Lovenox?

Yes, the active ingredient in Clexane Duo is enoxaparin sodium, which is also the active ingredient found in the major brand Lovenox in other regions.

Despite having the same medicine, regulatory documents often caution that the specific injection devices for different brands may not be interchangeable.


Q: Can Clexane Duo cause fatigue or dizziness?

Official adverse effect profiles mention that dizziness and headache are reported effects. Fatigue is not typically listed as a common side effect.

If unexpected or severe symptoms occur, the product label advises contacting a health professional.


Q: What blood tests are usually monitored while a person is using Clexane Duo?

Routine general coagulation tests (like PT or INR) are usually not necessary while using this medicine.

Regulatory information, however, recommends monitoring the Complete Blood Count (CBC), which includes the platelet count, and regular checks of renal (kidney) function. Anti-Factor Xa activity levels may be monitored in high-risk patients.


Q: What are the signs of a serious or rare side effect from Clexane Duo?

Official documents highlight the risk of serious side effects like Major Hemorrhage (severe bleeding) and rare reactions like Anaphylaxis (a severe allergic reaction).

Signs of major bleeding may include unusual bruising, persistent nosebleeds, or blood in stool or urine. Patients are generally informed about these documented risks.


Q: What is the purpose of the second active ingredient in Clexane Duo?

Official regulatory sources consistently confirm that Enoxaparin Sodium is the sole active ingredient in this medication.

This suggests the name 'Duo' is likely related to regional marketing or the device design, and does not imply a second active medicine.


Q: Can people with liver or kidney issues use Clexane Duo?

Kidney issues: Yes, but official guidelines require dose adjustment for patients with severe renal impairment (poor kidney function).

Liver issues: Caution is required with severe liver impairment, as regulatory documents note that the impact on drug exposure has not been fully investigated.


Q: What should be done if the injection site becomes painful or swollen?

Injection site reactions, including pain and bruising, are listed as common side effects. Administration guidelines note that you should not rub the injection site after injection to help minimize bruising.

If the area develops persistent swelling or severe pain, official guidance advises seeking follow-up with a healthcare provider.


Q: Is Clexane Duo used to treat stroke or prevent a second one?

The medicine is contraindicated (must not be used) in patients who have recently had a Hemorrhagic Stroke (bleeding in the brain).

While it is indicated for the treatment of certain acute heart conditions, it is not generally indicated for routine stroke prevention.


Q: Does the efficacy of Clexane Duo change if I gain or lose a lot of weight?

Yes, body weight is an important factor. Official guidelines state that dosing for the treatment of existing clots is often weight-based (calculated per kilogram of body weight).

Furthermore, patients who are at low weight or who are obese may require additional monitoring due to altered drug exposure.


Q: How does Clexane Duo compare to warfarin in terms of mechanism or use?

Mechanism: This medicine primarily inhibits the clotting enzyme Factor Xa, while warfarin works differently by blocking the production of several clotting factors that depend on Vitamin K.

Use: Due to its rapid onset and short half-life, it is often used for shorter-term needs, such as during the period when a patient temporarily stops taking an oral medicine like warfarin before a procedure.


Q: What is the definition of the 'contraindications' listed for Clexane Duo?

Contraindications is the term used in official regulatory documents to describe conditions or factors where a medical treatment must not be used because of the potential for harm.

The official label lists specific medical conditions where this drug is strictly prohibited.


Q: Does Clexane Duo have an effect on cholesterol levels?

Clinical research reviewed in regulatory-linked documents has indicated that the medicine is not associated with significant changes in serum lipids, which include cholesterol and triglyceride levels, during the course of treatment.


Q: Are there different strengths or types of Clexane Duo injections?

Yes, the medicine is available in multiple different strengths (measured in milligrams or International Units) in pre-filled syringes.

Different strengths are used by health professionals depending on the patient's weight, the condition being treated, and whether the medicine is for treatment or prevention.


Q: Can Clexane Duo be taken if I have a known allergy to other anticoagulant drugs?

The official label states that the drug is contraindicated if you have a known allergy (hypersensitivity) to enoxaparin, other heparins, or pork products.

The risk of cross-reactivity with blood thinners that are not in the heparin family is not specifically addressed in the regulatory documents.


Q: How does Clexane Duo function to break down existing clots?

Official information clarifies that this medicine's main function is to prevent new blood clots from forming or existing clots from growing larger by inhibiting a protein called Factor Xa.

It does not break down existing clots; this is the role of a different class of medicines called thrombolytics.


Q: What official studies address the safety of Clexane Duo in breastfeeding mothers?

Regulatory-linked information suggests the medicine has a high molecular weight and is not expected to be excreted into breast milk in significant amounts or absorbed by the infant.

For this reason, official safety information often concludes that no special precautions are generally required during breastfeeding.


Q: Does the combination of ingredients in Clexane Duo offer a unique benefit?

Official regulatory sources, such as the FDA, confirm that Enoxaparin Sodium is the sole active ingredient of this medication.

The name 'Duo' is related to regional branding or the injection device and does not imply a unique benefit from a combination of active drug substances.


Q: Can Clexane Duo cause a severe allergic reaction, and what are the symptoms?

Severe allergic reactions (anaphylaxis) are documented in official safety information as a rare, but serious, adverse event.

Signs of a severe reaction can include difficulty breathing, swelling of the face or throat, or collapse. The product label advises seeking immediate medical attention if signs of a severe reaction occur.


Q: Is it okay to store Clexane Duo in the refrigerator?

Official storage guidelines specify storing the medicine at Controlled Room Temperature (generally below 25 C) and explicitly state that it must not be frozen.

It is recommended to keep the product within the temperature range specified on the packaging to maintain its stability.


Q: What happens if Clexane Duo is accidentally injected into a muscle instead of under the skin?

This medicine is specifically intended for subcutaneous injection (under the skin), and regulatory information advises that intramuscular administration (into the muscle) is generally avoided.

Using the wrong route may increase the risk of localized bleeding, such as a hematoma, and could impact how well the medicine is absorbed.


Q: Are there public documents available detailing the clinical trial results for Clexane Duo?

Yes. While full trial details can be complex, results from the main clinical studies are reviewed and summarized in public-facing documents.

These include FDA Review Documents and various analyses accessible through government health databases.


Q: What is the recommended approach if a person needs emergency surgery while on Clexane Duo?

The approach is highly individualized, but official guidelines cover the management of this medicine when a patient requires a procedure with a high risk of bleeding.

The rules often mandate stopping the medication for a specified period, typically at least 12 to 24 hours, before major surgery. The decision to restart treatment after surgery is also carefully managed based on the bleeding risk.


Q: Does Clexane Duo have a generic version available?

Yes. The active ingredient, enoxaparin sodium, is available in generic or biosimilar products.

However, official regulatory documents emphasize that the specific pre-filled syringe devices can differ between brands and they may not be considered interchangeable from a technical standpoint.

How should Clexane Duo be stored and disposed of?

Storage and Disposal of Clexane Duo (Enoxaparin Sodium)

The official storage and disposal requirements for Clexane Duo (enoxaparin sodium) are mandated by regulatory agencies to ensure product stability and safety.


Storage Requirements

Clexane Duo must be stored at Controlled Room Temperature, which is generally below 25 C (77 F). It is a mandatory instruction to not freeze the syringes and to protect them from moisture and direct heat. Keep the pre-filled syringes in their original carton until the time of use and out of the sight and reach of children.


Disposal Instructions

Clexane Duo syringes are for single use only. All used syringes and needles are considered sharps and must be placed immediately into a dedicated, puncture-resistant sharps container. Do not dispose of used sharps in household trash. Final disposal of the full sharps container must strictly follow local authority guidelines for pharmaceutical waste.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

Available in countries:

Equivalent of Clexane Duo found in:

A-Z Index: