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Last reviewed: November 2020
Currently under review
If you’ve been prescribed adalimumab, or are considering it as an option, you’re not alone. Adalimumab is a common treatment for people with Crohn’s Disease and Ulcerative Colitis.
Our information can help you decide if this treatment is right for you. It looks at:
This is about adalimumab in general and should not replace advice from your health professional. For more information, talk to your IBD team or read the leaflet that comes with your medicine. You can also check the website: medicines.org.uk
We need your help to improve our information to better support people with Crohn’s and Colitis. Fill in our short survey to let us know what we're doing well and how we can better meet your needs.
Adalimumab is also known by the brand names Amgevita, Hulio, Humira, Hyrimoz, Idacio, Imraldi and Yuflyma. It will be prescribed by brand name.
Humira was the first brand of adalimumab. Amgevita, Hulio, Hyrimoz, Idacio, Imraldi and Yuflyma are ‘biosimilars’ of Humira but work in the same way. They are very similar to Humira with the same treatment effects. But there are some slight differences, such as how the injection device works. They also may contain different ingredients to prolong shelf-life. For more about biosimilars see our information on biologic medicines.
Adalimumab is a man-made antibody. The antibody is made from living cells, so it’s known as a biological medicine.
Adalimumab targets a protein in the body called tumour necrosis factor-alpha (TNF-alpha). TNF-alpha is naturally produced by your body. It plays an important role in helping your immune system fight infections. But too much TNF-alpha can damage the cells lining the gut. This is thought to partly cause the gut inflammation of people with Crohn’s or Colitis. Adalimumab binds to TNF-alpha, blocking its harmful effects and reducing inflammation. This helps to relieve symptoms.
You may also hear adalimumab called an ‘anti-TNF’ medicine. Other anti-TNF medicines are:
Adalimumab is used to treat:
It may be given to you if other treatments (such as steroids or immunosuppressants, like azathioprine, mercaptopurine or methotrexate):
You are being offered adalimumab to try to get your Crohn’s or Colitis into remission. Keeping your Crohn’s or Colitis under control is good for your long-term health. It reduces your risk of complications and of needing surgery.
Adalimumab may also:
Adalimumab is also to treat rheumatoid arthritis, ankylosing spondylitis, psoriasis, hidradenitis suppurativa and uveitis.
There are lots of things to think about when you start a new treatment. Your IBD team will discuss your options with you. When thinking about a new treatment you might want to consider the potential benefits, possible risks and the goals of your treatment. Some things to think about include:
Our Appointment guide has a list of questions you might want to ask. It can help you focus on what matters most to you. You might find our information about other medicines and surgery for Colitis helpful.
Use this tool to understand more about potential treatment options that suit your needs. The tool is designed to help you:
Adalimumab can be effective at getting and keeping your Crohn’s or Colitis under control (in remission).
To see how effective a medicine is, we can look at data from clinical trials. Clinical trials are used to test a medicine. However, this data may not completely represent what happens when medicines are given to you by your IBD team. In clinical trials, people are often removed from the trial if they do not respond quickly to a medicine. This won’t happen when you start taking adalimumab. Your IBD team may advise you take it for a longer time to see if you respond. They’ll also make sure the dose is right for you before suggesting you stop taking it. This means adalimumab may be more effective than the data from clinical trials shows.
The best clinical trials include people who were not taking the medicine. This is known as a placebo or control group. This is important. It allows us to see how many people have got better because of the medicine, as well as people who may have got better anyway (without the medicine).
The table below shows data from clinical trials of adalimumab in adults with moderate to severely active Crohn’s Disease.
More than twice as many people had their Crohn’s under control (in remission) after taking adalimumab for one year compared with people who had not been taking adalimumab (placebo). But, not everyone responds to adalimumab.
The table below shows data from clinical trials of adalimumab in adults with moderate to severely active Ulcerative Colitis.
Twice as many people had their Colitis under control (in remission) after taking adalimumab for one year compared with people who had not been taking adalimumab (placebo). But, not everyone responds to adalimumab.
Everyone responds differently when taking a new medicine. You may feel better soon after starting treatment – but it may take up to 12 weeks if you have Crohn’s, or up to eight weeks if you have Colitis.
However, adalimumab doesn’t work for everyone. It’s important that you are checked by your IBD team to see how well it is working for you.
Adalimumab is given as an injection under the skin. Adalimumab cannot be taken by mouth as a tablet because it would be destroyed by your digestive system.
Your treatment will be supervised by your IBD team. The first dose is usually given in hospital, or by a trained nurse at home. You will then be trained to inject it yourself. If you prefer, it may be possible for someone else, such as a family member, to be trained to give you the injections.
Adalimumab for adults comes ready to use in either a pre-filled syringe or a pre-filled injection pen. You may not see the needle in the injection pen, as it’s inside. The syringes or pens come in a pack. The pack contains an alcohol pad to clean your skin before injecting.
Adalimumab for children may either come as a pre-filled syringe or pre-filled pen, or in a vial (small bottle). The vial is designed to fit onto a syringe using an adapter. Only the brand Idacio comes in a vial.
Adalimumab will usually be sent to your home by a special delivery company. Adalimumab can only be prescribed by a specialist in the hospital. It is not a medicine that your GP can prescribe for you to pick up from your local pharmacy. You won’t have to pay for your adalimumab prescription, as long as you’re entitled to NHS care.
Adalimumab should be kept in the fridge. But, if you are travelling, it can be stored at room temperature (25°C) out of sunlight for up to:
Always check the leaflet that comes with your medicine. If it’s not used within this time you will need to get rid of it. Do not put it back in the fridge. Unused medicines should be disposed of safely by your pharmacist. Find out more about travelling with medicines in our information on Travel.
Make sure that you know how your injection device works. Different brands of adalimumab use different methods. For some, you’ll need to pinch your skin before you inject, or you may need to press a button to inject the medicine.
Pain at the injection site is a common side effect. You may also get redness, itching and swelling. You should expect to feel some pain, but these tips can help to make it easier to manage:
If you still have problems with injecting, ask your IBD team for help.
You’ll have your first induction dose followed by another induction dose two weeks later. The induction doses are higher to give a fast response. In children this may be increased to give a quicker response. You’ll then have maintenance dosing every two weeks if you respond well.
If adalimumab doesn’t work for you, or it becomes less effective, your doctor may suggest that you try a higher dose or dosing every week. This will be based on your symptoms, blood test results and the levels of medicine in your blood. Speak to your IBD team if you think this treatment is not working as well as it should be. You must not make any dose changes unless your IBD team have told you to.
You may need more than one injection for your induction doses if your adalimumab contains 40mg of the medicine.
You are likely to have a planned course of treatment for up to a year if adalimumab is working well for you. After that, your treatment plan may be extended. You will be checked at least every 12 months to make sure adalimumab is still right for you.
There are a few reasons why you and your IBD team may think it’s right to stop or change your treatment:
You have a right to take part in decisions about your treatment. Tell your IBD team what matters most to you, so they can give you the information and support you need. Our Guide to Appointments can help you have these conversations. Do not stop taking your medicine unless your IBD team have said it’s ok. If you have to stop taking this medicine but you’re still unwell, you may be able to try a different biologic. See our information on biologic medicines.
You may take adalimumab with other medicines for your Crohn’s or Colitis, such as 5-ASAs (like mesalazine), thiopurines (azathioprine or mercaptopurine) or methotrexate. Taking more than one medicine is known as combination therapy. For more on this, see our information on taking medicines.
Taking a combination of adalimumab with azathioprine or methotrexate may be more effective. This can reduce the risk of adalimumab becoming less effective over time. Speak to your IBD team about the risk of extra side effects with combination therapy. You should decide together what the best treatment option is for you.
Checks before treatment – such as blood tests and imaging – are important to make sure that adalimumab is right for you.
To help your IBD team, tell them if you have a history of:
And tell your IBD team if:
You’ll need regular checks while taking adalimumab, including blood tests. This helps your IBD team fit your treatment to your needs. It can help make sure that any problems with treatment are avoided or caught at an early stage. Tell your IBD team if you notice any new symptoms or side effects.
Blood tests may be used to check the levels of adalimumab in your blood and to see if you’ve developed antibodies. This helps your IBD team to see if the treatment is working or if your dose needs changing.
It’s important that you attend your appointments and have blood checks to make sure this medicine is prescribed safely.
If you feel dizzy or tired after taking this medicine do not drive or use any tools or machines.
This medicine affects the way your immune system works. Your immune system is still able to fight off infections, just not quite as well as other people. You may find that infections affect you more than they used to, or it takes you longer to recover. Tell your IBD team if you develop signs of an infection, such as a sore throat, fever or any new symptoms that concern you. They may advise you to wait until you feel better before injecting. Less often, more serious infections can be a side effect of adalimumab. See the section below on Side effects.
Even though your risk of complications may be higher when taking adalimumab, it shouldn’t stop you from living life as before. There are a few extra precautions your IBD team may advise you to take to keep safe and reduce your risk:
All medicines can have unwanted effects, although not everyone will get them. Some side effects can happen right away, others may happen later. Some can even last for a short time after you stop treatment.
Some side effects may be mild and go away on their own or when the medicine is stopped. Others may be more serious and will need managing, or may mean that the treatment is not right for you. Try to consider how unwell any side effects are making you feel, as well as the benefits of taking this medicine to keep your Crohn’s or Colitis under control.
Speak to your IBD team if you experience any side effects.
Around 1 in every 10 people taking adalimumab may have:
Common: Somewhere between 1 in every 10 people to 1 in every 100 people taking adalimumab may develop this side effect.
Uncommon: Somewhere between 1 in every 100 people to 1 in every 1000 people taking adalimumab may develop this side effect.
Rare: Somewhere between 1 in every 1000 people to 1 in every 10,000 people taking adalimumab may develop this side effect.
This is not a full list of side effects. For more information see the Patient Information Leaflet provided with your medicine or visit medicines.org.uk/emc/.
We encourage you to report any side effects to the Medicines and Healthcare Products Regulatory Agency (MHRA) through the Yellow Card scheme. Your doctor should also report it. Report your side effect at yellowcard.mhra.gov.uk.
Adalimumab is often taken alongside other medicines safely. See the earlier section Taking adalimumab with other Crohn’s or Colitis treatments.
However, adalimumab may interact with some medicines. Speak to your doctor or pharmacist if you’re taking, or plan to take any other medicines. This includes over-the-counter medicines (medicines that you buy yourself) and any herbal, complementary, or alternative medicines or therapies.
Do not take medicines that contain anakinra or abatacept. These medicines are commonly used for Rheumatoid Arthritis.
Tell any doctor, dentist or health professional treating you that you are taking adalimumab. Always carry the alert card that comes with the medicine while you are taking it and for up to six months after your last dose.
It’s not safe to have ‘live’ vaccines while taking adalimumab. It can take up to four months after your last dose for adalimumab to completely leave your body. However, it’s safe to have live vaccines 3 months after your last dose. Ask your IBD team to make sure your vaccinations are up to date before you start adalimumab, or if you’re planning to travel. If you’ve recently had a live vaccine you may have to wait 4 weeks before starting adalimumab.
In the UK, live vaccines include:
Everyone with Crohn’s or Colitis taking a biologic medicine should have the yearly flu vaccine. This is not a live vaccine and is safe to have while taking adalimumab.
If someone you live with is due to have a live vaccine, ask your IBD team if you need to take any precautions.
Adalimumab does not affect fertility. If you don’t want to get pregnant you should use contraception.
Talk to your IBD team if you're taking adalimumab and planning a pregnancy or are already pregnant. If you decide to continue taking adalimumab, it should not stop you having a normal pregnancy and a healthy baby. Research shows that anti-TNF medicines, like adalimumab, do not affect your pregnancy, or harm your baby. Long-term health, infection rates and development do not appear to be affected in children of mothers taking anti-TNFs during pregnancy. This includes mothers who took anti-TNFs until birth.
Adalimumab does not appear to affect foetuses, but there hasn’t been enough research to rule out the possibility completely. To be cautious, drug companies state that adalimumab should only be used during pregnancy if needed to keep your condition under control. This is because the medicine could cross the placenta. They recommend using contraception to prevent pregnancy while taking adalimumab and for at least five months after your last dose. However, adalimumab is generally considered safe. Your IBD team may advise the safest option is to keep taking it during pregnancy, to keep your Crohn’s or Colitis under control.
When deciding whether to continue taking adalimumab, you should also consider the risks of having a flare-up while you’re pregnant. Having active Crohn’s or Colitis can lead to premature (early) birth, low birth weight and higher rates of miscarriage. It’s important to keep your condition under control in pregnancy. If your Crohn’s or Colitis is well controlled (remission), your IBD team may recommend you take adalimumab for the first six months (first and second trimesters), but stop during the third trimester. This aims to reduce the exposure to your baby. If your condition is not well controlled, your IBD team may recommend you take adalimumab throughout your entire pregnancy to keep you well.
Taking adalimumab during pregnancy is likely to affect when your baby can have any live vaccines. This includes the BCG for tuberculosis and the rotavirus vaccine. It should not affect the rest of your baby’s vaccination schedule.
National guidance advises that if you take adalimumab during your pregnancy your baby should not have live vaccines until they are at least six months old. However, adalimumab drug companies advise that your baby should not have any live vaccines for five months after your last adalimumab dose during pregnancy.
You must tell your baby’s healthcare team you were taking adalimumab while pregnant. Decisions on what vaccines your baby should have and when they should have them needs to be made on an individual basis. Your IBD team and midwife should be able to help you come to a decision.
Take extra care if your baby does have the rotavirus vaccine, as live virus can be shed in the baby’s poo for up to 14 days. Make sure you wash your hands and/or wear gloves when changing their nappy.
There is some evidence that your baby may be more prone to infections if you take azathioprine or mercaptopurine along with anti-TNFs, like adalimumab, during pregnancy.
Discuss the risks and benefits of taking adalimumab while pregnant with your IBD team. You can find out more in our information on Pregnancy and Reproductive Health.
There is less research on men wanting to father a child while taking anti-TNFs. But it’s generally considered safe for a man to conceive a child.
You can take adalimumab while breastfeeding. Small amounts of adalimumab have been found in breast milk, but adalimumab has not been found in breastfed babies. Adalimumab is destroyed by the digestive system when taken orally, so it wouldn’t be absorbed by your baby.
Small studies of babies breastfed by mothers taking adalimumab have shown normal growth, development and rates of infection. Speak to your IBD team if you’re worried.
Alcohol is not known to interact with adalimumab.
Taking medicines and managing side effects can be difficult – we understand and we’re here to help. Our Helpline can answer general questions about treatment options and can help you find support from others with the conditions.
Your IBD team are also there to help. You can talk to them about your dosage, how they’ll be monitoring you and what alternatives may be available. You should also get in touch with your IBD team if you have any new symptoms or side effects.
It can take time to find the medicine that’s right for you. Don’t be afraid to ask questions and seek out extra support when you need it.
This information is general and doesn’t replace specific advice from your health professional. Talk to your doctor or IBD team for more information. You can also check the Patient Information Leaflet that comes with your medicine or visit medicines.org.uk/emc/.
Health professionals can order some publications in bulk by using our online ordering system. If you would like a printed copy of any of our information, please contact our helpline.
Our helpline is a confidential service providing information and support to anyone affected by Crohn's or Colitis. Our team can:
Email helpline@crohnsandcolitis.org.uk
This closed-group community on Facebook is for everyone affected by Crohn's or Colitis. You can share your experiences and receive support from others.
Our Local Networks of volunteers across the UK organise events and provide opportunities to get to know other people in an informal setting, as well as to get involved with educational, awareness-raising and fundraising activities. You may find just being with other people and realising that you are not alone can be reassuring. Families and relatives may also find it useful to meet other people with Crohn's or Colitis. All events are open to members of Crohn’s & Colitis UK.
We follow strict processes to make sure our information is based on up-to-date evidence and easy to understand.
Please email us at evidence@crohnsandcolitis.org.uk if:
You can also write to us at Crohn’s & Colitis UK, 1 Bishop Square, Hatfield, AL10 9NE, or contact us through our Helpline: 0300 222 5700
We know it can be difficult to live with, or support someone living with these conditions. But you’re not alone. We provide up-to-date, evidence-based information and can support you to live well with Crohn’s or Colitis.
Our helpline team can help by:
Providing information about Crohn’s and Colitis.
Listening and talking through your situation.
Helping you to find support from others in the Crohn’s and Colitis community.
Providing details of other specialist organisations.
Please be aware we’re not medically or legally trained. We cannot provide detailed financial or benefits advice or specialist emotional support.
Please contact us via telephone, email or LiveChat - 9am to 5pm, Monday to Friday (except English bank holidays).
If you need specific medical advice about your condition, your GP or IBD team will be best placed to help.
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