Druggist Menu
Post Highlights

New Warfarin Alternatives: Everything You Need To Know

New Warfarin Alternatives

Warfarin is the most used anticoagulant in the UK, with a history going back to the 1950s when it was approved for human use in 1954. Over 60 years later and the popularity of warfarin is indisputable. Two factors contributing to the wide use of warfarin are the effectiveness and low cost of the drug.

However, as you are about to learn from this post, the prescribing of warfarin is in decline in place of warfarin alternatives, a new group of novel anticoagulant drugs known as Non-Vitamin K antagonist oral anticoagulants (NOAC).

What Are Anticoagulants Used For?

Anticoagulants are drugs that prevent the formation of blood clots in the body. The formation of a blood clot can lead to serious health emergencies such as stroke and heart attack. Anticoagulants can be used in the treatment and/or prevention of clot formation in the following conditions:

  • Venous thromboembolism (VTE):
  • deep vein thrombosis (DVT): formation of a blood clot in the vein located in the leg
  • pulmonary embolism: blood clot travels in the blood and blocks to blood vessels located in the lungs
  • Atrial fibrillation (irregular heartbeat): Patients with atrial fibrillation are at risk of having a stroke as a consequence of clot formation.
  • Patients who had transient ischaemic attacks “mini-stroke.”

Quick FAQ

What is the most effective blood thinner with the least amount of side effects?
Apixaban, for example, was linked to the lowest risk of serious bleeding.
Warfarin alternative drugs can be used in DVT treatment
Deep Vein Thrombosis (DVT): a blood clot formation in the vein of the leg
Alternative drugs to warfarin can be used in PE treatment
Pulmonary embolism is caused by a blood clot that travels to the vein in the lungs

What Is Warfarin?

Warfarin: Treatment Indications

Warfarin is an anticoagulant drug that prevents the formation of clots in the blood.

Commonly known as a blood thinner, warfarin is used in:

  • Treatment and prevention of deep vein thrombosis (DVT)
  • Treatment and prevention of pulmonary embolism
  • Prevention of clot formation in patients with atrial fibrillation.
  • Prevention of clot formation in patients with prosthetic heart valve
  • Patients who had transient ischaemic attacks (“mini-stroke”)

Warfarin: Mechanism Of Action

Warfarin stops the production of Vitamin K, which is needed to produce a blood clot.

Warfarin is taken daily, at the same time of the day, according to the dose set by blood tests (coagulation tests), which tells how much time it takes for blood to clot. This parameter is known as the International Normalised Ratio (INR).

Each patient has an INR target, usually set at 2.5 with an acceptable range between 2-3; however, the INR target can differ, depending on the indicated use. It is very common for INR to change. If this happens, patients need to adjust their dose by increasing or decreasing the number of tablets they take.

Warfarin comes in three different tablet strengths:

  • Warfarin 0.5mg
  • Warfarin 1mg
  • Warfarin 3mg

Advantages of warfarin treatment

  • Effective
  • A long history of use
  • Cheap
  • In an emergency, the actions of warfarin can be reversed, for example, with Vitamin K.

Disadvantages of warfarin treatment

  • It takes a few days to work (slow onset of action)
  • Frequent monitoring (blood test to check INR) and dose adjustments are needed
  • Narrow therapeutic window: small changes in the drug concentration (how much drug is in the body) for example, due to interaction with another drug or major dietary changes can cause significant side effects (thrombosis: clotting of the blood if INR below 2 or risk of bleeding if INR above 3)
  • Interacts with many drugs, including over-the-counter drugs (OTC).
  • Dietary restrictions and interaction with food containing Vitamin K

Warfarin Alternatives: Non-Vitamin K Antagonist Oral Anticoagulants (NOAC)

medicine tablets

Novel anticoagulants, Non-Vitamin K Antagonist Oral Anticoagulants (NOAC), work differently to warfarin.

In simple terms, this group of alternative warfarin drugs stops the production of chemicals (enzymes) needed in the production of fibrin

a compound (protein) that plays a role in the clotting of the blood.

Currently, four NOACs are licensed in the UK:

  • Rivaroxaban (brand name: Xarelto)
  • Dabigatran (brand name: Pradaxa)
  • Apixaban (brand name: Eliquis)
  • Edoxaban (brand name: Savaysa)

Main advantages over warfarin alternatives

  • Fast onset of action (the time it takes to work), for example, rivaroxaban and dabigatran, start to work within 30 mins after oral administration (Brighton, 2010)
  • Fewer drug interactions than warfarin
  • Fewer interactions with food
  • More predictable actions of the drug
  • Monitoring (blood tests) not required
  • Simple dosing as compared with warfarin
  • Lower incidence of major bleeding

Warfarin alternative drugs: main disadvantages

  • Currently, a significantly higher cost of each drug as compared with warfarin.
  • In an emergency, for example, trauma or surgery, NOACs have no antidote (to decrease the risk of bleeding), apart from dabigatran. Some NOAC ‘antidote’ drugs are in different stages of development (Levy et al. 2018)

Warfarin Vs. Warfarin Alternatives: Prescribing Statistics In The UK

The graph below represents the number of items prescribed for each anticoagulant in the UK between 2015 and 2018. Data from 2019 was excluded as prescribing information is not provided yet for the whole of 2019.

Although warfarin is still the most prescribed oral anticoagulant in the UK, you can easily see that the number of prescriptions issued for this drug has decreased each year.

Newer anticoagulants such as apixaban and rivaroxaban have been gaining popularity quickly at the expense of warfarin. Looking at the current growth trend, one would expect to see apixaban and rivaroxaban becoming more prescribed drugs than warfarin in the next few years.

1. Dabigatran (Brand Name: Pradaxa) As An Alternative To Warfarin

Dabigatran was the first approved ‘novel’ anticoagulant. Dabigatran is licensed in the prevention of blood clot formation in patients who had total hip or knee replacement surgery. Patients who had one of these surgeries are at higher risk of blood clot formation in the vein located in a leg (DVT).

dabigatran 110mg tablets

Dabigatran is also licensed for stroke prevention in patients with nonvalvular atrial fibrillation, who also have an additional risk factor, for example, hypertension, diabetes, heart failure, previous stroke, or ‘mini’ stroke or patients who are 75 years of age or older.

Additional indications for dabigatran include:

  • Treatment of deep vein thrombosis (DVT)
  • Treatment of pulmonary embolism (PE), and
  • Prevention of recurrent DVT and PE

Pradaxa capsules come in three different strengths:

  • 75mg capsule
  • 110mg capsule
  • 150mg capsule

How to take dabigatran?

The dose depends on the condition being treated and the timing of the treatment; for example, the initial dose may differ from the usual maintenance dose. Follow your prescriber’s directions on Pradaxa dosing.

Dabigatran can be taken with or without food. Capsules should not be open, as this may increase the risk of bleeding (eMC, 2019).

Dabigatran side effects

Dabigatran use is associated with a number of possible side effects. The likelihood of some side effects depends on the condition being treated.

Possible, common side effects experienced by up to 1 in 10 patients taking dabigatran relate to the risk of bleeding, for example, nose bleeds, bleeding from penis/vagina, rectum, or gums.

Other common side effects include:

  • Indigestion
  • Feeling sick
  • Stomach ache
  • Loose bowel movements

Rarely dabigatran may cause serious bleeding, which may lead to disability or become life-threatening or may lead to death.

Please refer to the patient information leaflet (PIL) for more details on possible side effects and how to recognize serious side effects. A link for PIL is included at the end of this post.

2. Warfarin Alternatives: Rivaroxaban (Brand Name: Xarelto)

Rivaroxaban is licensed to prevent venous thromboembolism, such as DVT in patients who had hip or knee replacement surgery.

Additionally, rivaroxaban is licensed in treating DVT and PE and preventing both conditions from happening again. The treatment duration and dose depend on the condition being treated or prevented.

The usual dose of rivaroxaban can range from 10mg to 20mg taken daily or twice daily. Follow the directions of your prescriber for dosing instructions.

How to take rivaroxaban?

Rivaroxaban is taken with or after food. Xarelto tablets can be crushed and mixed with water in patients with swallowing difficulties.

The patient information leaflet states that rivaroxaban can be taken with or without food. In July 2019, The Medicines and Healthcare products Regulatory Agency (MHRA) issued a drug safety update recommending that rivaroxaban 15mg and 20mg (only) should be taken with food as decreased effectiveness was observed when 15mg or 20mg tablets were taken on an empty stomach (Gov.uk, 2019).

Rivaroxaban: what are the most common side effects?

The most common side effects (1 in 10 patients) associated with the use of rivaroxaban were bleedings:

  • Nose bleeds
  • Gastrointestinal bleeding (in the stomach)
  • Bleeding from gums
  • Heavy menstrual periods
  • Bleeding into eye
  • Bleeding under or from the skin

Other common side effects:

  • Rash, itchy skin
  • Indigestion, stomachache, constipation, diarrhea
  • Felling or being sick
  • Weakness, tiredness
  • A decrease in blood pressure
  • Fever
  • Change in liver or kidney
  • Change in liver enzymes and kidney functions

Rarely rivaroxaban can cause severe skin reactions. Refer to the product information leaflet for details about more serious, rare side effects and how to recognize them. Link is given at the end of the post.

3. Apixaban (Brand Name: Eliquis) As An Alternative To Warfarin

Apixaban is licensed for:

  • Prevention of blood clot formation in patients who had hip or knee replacement
  • Prevention of blood clot formation in the heart due to the irregular heartbeat (atrial fibrillation)
  • To treat blood clots associated with DVT and PE and to prevent re-occurrence of blood clots in both conditions.

How to take apixaban?

Apixaban is usually taken twice a day. Recommended dosage may vary depending on the condition being treated and timing; for example, starting dose may be different from the maintenance (usual) dose. Apixaban (Eliquis) comes as 2.5 and 5mg tablets.

Apixaban can be taken with or without food at the same time every day.

Apixaban common side effects

As with other anticoagulants, common side effects for apixaban relate to the risk of bleeding, which very rarely can be life-threatening (bleeding in the brain).

The possibility of common side effects vary and depend on the condition treated. See the product information leaflet for more details on side effects and their frequency (eMC, 2019).

Common side-effects associated with apixaban use include:

  • Hemorrhage (bleeding from the nose, gums, urine, in the stomach, mouth, or the vagina)
  • Bruising ad swelling
  • Contusion
  • Epistaxis (nose bleeds)
  • Hematoma (bruising)
  • Anemia (can cause tiredness)
  • Feeling sick
  • Skin rash

I contrasted apixaban vs warfarin in more detail in another post.

Quick FAQ

Is warfarin Safer Than eliquis?
Eliquis was proven to be more effective than warfarin at reducing stroke and systemic embolism risk.

4. Edoxaban (Brand Name: Lixiana) As Warfarin Alternative

Edoxaban is used for the prevention of strokes in patients with atrial fibrillation, and prevention of blood clot formation in other parts of the body, in patients who have an additional risk such as hypertension, diabetes, heart failure, previous stroke, or ‘mini’ stroke or patients who are 75 years of age or older.

Additionally, edoxaban is licensed to treat and prevent blood clots in the veins of the leg (DVT) and the blood vessels in the lungs (PE).

Edoxaban comes in the form of:

  • 15mg tablets
  • 30mg tablets and
  • 60mg tablets

How to take edoxaban?

Dose, duration of treatment depends on the condition treated. Edoxaban can be taken with or without food. Follow the directions of your doctor on how to take edoxaban.

Edoxaban: common side effects

Similar to all other anticoagulants, edoxaban can cause bleeding, which can be life-threatening in rare cases. Common side-effects associated with edoxaban include:

  • Anemia (can cause tiredness)
  • Headaches
  • Dizziness
  • Nose bleeds
  • GI side effects (lower and upper gastrointestinal hemorrhage/bleeding, abdominal pain, oral bleeding or bleeding of pharynx, nausea)
  • Hepatic disorders, foR example, an increase of bilirubin
  • Skin related side effects (rashes, itching, bleeding in the soft tissue)
  • Vaginal bleeding (for women under 50 years of age)

Refer to the product information leaflet for more information on side effects. The link is located at the end of this post.

Are Warfarin Alternatives Better Than Warfarin?

There are definite advantages of warfarin alternatives when anticoagulants are needed in treatment. Two important factors that need addressing are the safety and effectiveness of NOAC compared to warfarin. Below is the summary of conclusions taken from the main clinical trials comparing each individual NOAC with warfarin.

Dabigatran Vs. Warfarin: Effectiveness And Safety

A large trial (RE-LY) involving 18,113 patients compared the effectiveness of dabigatran and warfarin in stroke and clot prevention in patients with Nonvalvular Atrial Fibrillation (NVAF).

This study concluded that dabigatran is non-inferior (equivalent) to warfarin in the prevention of strokes or systemic clot formation (dose of dabigatran: 110mg). With this dose, dabigatran was associated with lower rates of major hemorrhage.

Lower rates of strokes and clot formation were observed when dabigatran was used at a dose of 150mg; however, similar rates for major bleeding were observed (Connolly et al., 2009).

Rivaroxaban Vs. Warfarin: Effectiveness And Safety

A ROCKET AF study compared the effectiveness of rivaroxaban and warfarin in stroke and systemic (in the body) clot prevention in patients with atrial fibrillation. It was concluded that rivaroxaban was non-inferior (equivalent) to warfarin in the prevention of strokes and systemic clots.

There was also no significant difference in the risk of major bleeding; however, treatment with rivaroxaban was associated with a lower incidence of bleeding in the skull (intracranial bleeding) and lower incidence of fatal bleeding (Patel et al. 2011).

The effectiveness of rivaroxaban was also compared in the treatment of an acute episode of deep vein thrombosis (DVT). Trail (EINSTEIN-DVT) involving 3449 patients with acute DVT. Patients were given either rivaroxaban or subcutaneous enoxaparin followed by a vitamin K antagonist (including warfarin).

Rivaroxaban was found to be non-inferior (equivalent) as ‘short-term’ and continued treatment of venous thrombosis, offering a straightforward, single-drug solution (EINSTEIN Investigators, 2010).

Apixaban Vs. Warfarin: Effectiveness And Safety

A study (ARISTOTLE) of 18,201 patients with atrial fibrillation who had an additional risk factor for a stroke compared the effectiveness of apixaban and warfarin in the prevention of ischemic (blood vessel in the brain blocked by a clot) and hemorrhagic strokes (rupture of blood vessel in the brain and consequent leak of blood in the brain). This trial also looked at major bleeds and deaths rates for any reason during the trial.

Main results from the trial (Granger et al. 2011):

  • Apixaban was found to be superior (better) to warfarin in stroke prevention/clots formation in patients with atrial fibrillation
  • Apixaban was associated with less bleeding
  • Lower deaths were recorded in the group treated with apixaban

Quick FAQ

What foods should I avoid when taking apixaban?
Avoid foods high in Vitamin K, e.g. big amounts of leafy green vegetables and some vegetable oils

Edoxaban Vs. Warfarin: Effectiveness And Safety

The main clinical trial involving edoxaban and warfarin compared the effectiveness of both drugs in the treatment of venous thromboembolism (for example, DVT – clot formation in a deep vein of the leg).

4921 patients who took part in this study received initial treatment with heparin (an injectable blood thinner) followed by either edoxaban or warfarin treatment.

Conclusions from the study (Hokusai-VTE Investigators, 2013):

  • Edoxaban was found non-inferior (equivalent) to standard treatment
  • Edoxaban was associated with (significantly) less bleeding in patients with venous thromboembolism

Switching From Warfarin To Warfarin Alternatives (NHS)

Switching treatment from warfarin to NOAC (apixaban, dabigatran, rivaroxaban, or edoxaban) is possible; however, it will depend on personal circumstances.

Generally, switching from warfarin involves (NICE, 2019):

  • Stopping the treatment with warfarin
  • Measurement of INR with ideal target INR to be less than 2
  • Treatment initiation with NOAC when INR is below 2
  • If INR is between 2 and 2.5 treatment commerce the next day
  • If INR is above 2.5, the start of a new treatment is delayed until INR drop below

Conclusion

Newer anticoagulants offer more advantages than disadvantages as compared to warfarin treatment. Well-designed and studied clinical trials confined all ‘newer’ anticoagulants are equivalently effective as warfarin, and in some cases, superior (better) to warfarin.

Patients who wish to switch their treatment from warfarin to an alternative anticoagulant should speak to their doctor in the first instance.

Warfarin And Warfarin Alternatives: Drugs Leaflets

  • Warfarin leaflet
  • Dabigatran: Pradaxa leaflet
  • Rivaroxaban: Xarelto leaflet
  • Apixaban: Eliquis leaflet
  • Edoxaban: Lixiana leaflet
References
  • Connolly SJ, Ezekowitz MD, Yusuf S, et al. Dabigatran versus warfarin in patients with atrial fibrillation. N Engl J Med. 2009;361(12):1139–1151. Available at: https://doi.org/10.1056/NEJMoa0905561 Accessed on 22/01/2020
  • Brighton Timothy (2010). New oral anticoagulant drugs - mechanisms of action. Available at: http://dx.doi.org/10.18773/austprescr.2010.017 Accessed on 19/12/2019
  • Bouhajib, M. and Tayab, Z., 2020. A Pharmacokinetic Evaluation of Dabigatran Etexilate, Total Dabigatran, and Unconjugated Dabigatran Following the Administration of Dabigatran Etexilate Mesylate Capsules in Healthy Male and Female Subjects. Drug research70(01), pp.33-40. Available at: https://www.thieme-connect.com/products/ejournals/html/10.1055/a-1025-0119 Accessed on 24/01/2020
  • EINSTEIN Investigators, Bauersachs R, Berkowitz SD, et al. Oral rivaroxaban for symptomatic venous thromboembolism. N Engl J Med. 2010;363(26):2499–2510. doi:10.1056/NEJMoa1007903 Available at: https://doi.org/10.1056/nejmoa1007903 Accessed on 22/02/2020
  • Stern, G.M., Pitlick, J.M., Stacy, Z.A. and Crannage, A.J., 2016. Conception of a personalized medication adherence discharge kit for rivaroxaban. Hospital Pharmacy51(1), pp.60-67. Available at: https://journals.sagepub.com/doi/abs/10.1310/hpj5101-60. Accessed on 24/02/2020
  • Granger CB, Alexander JH, McMurray JJ, et al. Apixaban versus warfarin in patients with atrial fibrillation. N Engl J Med. 2011;365(11):981–992. doi:10.1056/NEJMoa1107039 Available at: https://doi.org/10.1056/nejmoa1107039 Accessed on 22/02/2020
  • Hokusai-VTE Investigators, Büller HR, Décousus H, et al. Edoxaban versus warfarin for the treatment of symptomatic venous thromboembolism [published correction appears in N Engl J Med. 2014 Jan 23;370(4):390]. N Engl J Med. 2013;369(15):1406–1415. doi:10.1056/NEJMoa1306638 Available at: https://doi.org/10.1056/nejmoa1306638 Accessed on 22/02/2020
  • Levy, J., Douketis, J. & Weitz, J. (2018). Reversal agents for non-vitamin K antagonist oral anticoagulants. Nat Rev Cardiol 15, 273–281 (2018) doi:10.1038/nrcardio.2017.223 Available at: https://doi.org/10.1038/nrcardio.2017.223 Accessed on 19/12/2019
  • Patel MR, Mahaffey KW, Garg J, et al. Rivaroxaban versus warfarin in nonvalvular atrial fibrillation. N Engl J Med. 2011;365(10):883–891. doi:10.1056/NEJMoa1009638 Available at: https://doi.org/10.1056/nejmoa1009638 Accessed on 22/01/2020