Ambrisentan
What is ambrisentan?
Ambrisentan (brand name: Volibris, Viatris, Cipla, Pulmoris) is a medicine used to treat a condition called pulmonary arterial hypertension (PAH). This is a condition where there is increased pressure in the arteries that carry blood from the heart to the lungs.
PAH can occur in a number of rheumatological diseases such as scleroderma. These diseases can cause thickening of the blood vessel walls. Symptoms include shortness of breath during routine activity (such as climbing stairs), tiredness and chest pain.
How does it work?
Ambrisentan helps lower blood pressure in the lungs by opening up the lung blood vessels. This helps your heart pump blood through the blood vessels in the lungs more efficiently.
What benefit can you expect from your treatment and how is it monitored?
Ambrisentancan reduce the symptoms of PAH and in some cases prolong life expectancy. It may take up to 2 months or more before your symptoms start to improve.
Before ambrisentan can be prescribed, a specialist will assess you. This may be a rheumatologist, immunologist, cardiologist (heart) or a respiratory (lung) physician who has experience in managing PAH.
You will be asked to have the following tests:
• an ultrasound scan of your heart (echocardiogram)
• a right heart catheter – this is a test to measure the blood pressure in your heart and lungs. It involves inserting a tube into your heart from an artery in your neck, armor groin.
• a six minute walk test (6MWT) to measure how far you can walk in six minutes.
Every six months you will be asked to have the echocardiogram and the 6MWT to check that ambrisentan is still helping your condition.
How is ambrisentan taken?
Ambrisentan is a tablet. It comes in two strengths (5mg and 10mg).
What is the dosage and when should it be taken?
The normal starting dose is 5mg once a day. In some cases the dose may be increased by your doctor to 10mg once a day.
Ambrisentan should be taken at the same time each day. It is usually taken in the morning or at night. If you forget to take a tablet you can take it later in the day. If it is the next day, take the normal dose (do not take a double dose). It does not have to be taken with food.
Can other medicines be taken with ambrisentan?
Ambrisentan may be taken in combination with other medicines, including:
• steroid medicines such as prednisolone
• anti-inflammatory medicines (NSAIDs) such as naproxen (Naprosyn) or ibuprofen (Brufen/Nurofen) provided your kidney and heart function are normal
• pain-relieving medicines such as paracetamol and combined medicines such as Panadeine and Panadeine Forte
• calcium channel blockers (for Raynaud’s disease)
• diuretics (fluid tablets)
• warfarin (blood-thinning medicine) see Precautions
• other treatments for PAH.
There are a number of medicines that should not be taken when you are taking ambrisentan.
How long is the treatment continued?
Ambrisentan may be given on a long-term basis provided it does not cause problems and continues to help your condition. It is usually given for as long as the 6-monthly tests (echocardiogram and 6MWT) show that it is of benefit.
Do not stop taking ambrisentan without first talking to your doctor. If your doctor decides to stop the treatment, you may need to reduce the dose gradually before you stop the medicine completely.
Are there any side effects?
Most people who take ambrisentan do not experience side effects. Tell your doctor if you are worried about possible side effects. Having a lower dose may reduce side effects so that you can continue taking ambrisentan.
Most common possible side effects
• The most common side effects include stomach upset, nausea, diarrhea and headache.
• Other side effects include inflamed throat,irritated nose passages or skin rash.
• Dizziness due to low blood pressure, flushing, ankle and/or leg swelling can occur.
• Irregular heartbeats or tiredness have been reported.
Less common or rare possible side effects
• Ambrisentan can cause severe liver problems. Symptoms include nausea, stomach pain, low-grade fever, loss of appetite, dark urine, clay-coloured stools and jaundice (yellowing of the skin or eyes). Call your doctor at once if you have any of these symptoms.
• Low haemoglobin (anaemia) can be detected on blood tests but rarely causes symptoms.
• There are also a number of other rare side effects.
What precautions are necessary?
Blood tests
- Your liver function and blood counts for haemoglobin will need to be tested before you start taking ambrisentan, and again each month during your treatment.
Use with other medicines
- Ambrisentan can interact with other medicines. You should tell your doctor (including your GP, rheumatologist and other health professionals) about all medicines you are taking or plan to take. This includes over-the-counter or herbal/naturopathic medicines.
• The following medicines may interfere with ambrisentan. Some should not be taken with ambrisentan. For others, the dose may need to be adjusted.
− cyclosporin (Cicloral, Neoral, Sandimmune)
− cholesterol lowering medicines
− anti-fungal medicines
− HIV/AIDS medicines lopinavir or ritonavir (Kaletra, Norvir)
− tacrolimus (used to prevent rejection of liver or kidney transplants)
− rifampicin (used for tuberculosis). - Ambrisentan does not increase the risk of side effects from low-dose aspirin (taken for prevention of heart attack and strokes).
Vaccines
- Most vaccines can be given safely with ambrisentan. Pneumovax and yearly flu vaccinations are safe and recommended to reduce your risk of those infections. Talk with your rheumatologist before receiving any vaccines.
Use during pregnancy and breastfeeding
- Ambrisentan should not be taken during pregnancy or when breastfeeding.
- If you are a woman of child bearing age you should use effective contraception while taking ambrisentan.
- If you are planning a family or you become pregnant during your treatment, you should discuss this with your doctor as soon as possible.
How to store ambrisentan
- Store ambrisentan at room temperature, away from heat, moisture and light (e.g. not in the bathroom).
- Keep all medicines out of reach of children.
Important things to remember:
- While taking ambrisentan you should see your treating specialist regularly to make sure the treatment is working, and to minimise any possible side effects.
- Ambrisentan should be taken at the same time each day.
- You should not stop your treatment unless your doctor tells you to.
- You should not increase or reduce the dose of ambrisentan unless your doctor tells you to.
- Contact your doctor at once if you experience symptoms such as nausea, stomach pain, fever, loss of appetite, dark urine, clay-coloured stools or jaundice (yellowing of the skin or eyes).
- Ambrisentan interacts with many other drugs.
Discuss with your doctor whether you need to change the doses of these drugs or avoid using them together with ambrisentan.
For more information see the Ambrisentan – printable information sheet.
This Information Sheet has been prepared using materials obtained from various sources which have been reviewed by the Australian Rheumatology Association (ARA). It contains general information only and does not contain a complete or definitive statement of all possible uses, actions, precautions, side effects or interactions of the medicines referenced. This information is not intended as medical advice for individual conditions nor for making an individual assessment of the risks and benefits of taking a particular medicine. Decisions regarding the assessment and treatment of patients are the sole responsibility of the treating medical professional, exercising their own clinical judgment and taking into account all of the circumstances and the medical history of the individual patient. ARA has used all reasonable endeavours to ensure the information on which this Information Sheet is based is accurate and up to date. However, the ARA accepts no responsibility or liability for the accuracy, currency, reliability and/or completeness of the information contained in this Information Sheet. To the maximum extent permitted by law, the ARA expressly disclaims any liability for any injury, loss, harm or damage arising from or in connection with use of and reliance on the information contained in this Information Sheet. This information sheet is copyright and may be reproduced in its entirety but may not be altered without prior written permission from the ARA.Page updated October 2024Discover more...
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