Cancer drugs A to Z list
FLAG-Ida includes the drugs below. How to pronounce the drug names are in the brackets.
FL - fludarabine (flu-dara-bin)
A - Ara C, it is also known as cytarabine (sye-ta-ra-bin)
G - granulocyte colony stimulating factor (G-CSF)
Ida - idarubicin (eye-da-roo-biss-in)
Find your cancer type on our A-Z list
Cytarabine and fludarabine are a type of chemotherapy drug called an . Antimetabolites kill cancer cells by stopping them from making and repairing that they need to grow and multiply.
Idarubicin works by destroying quickly dividing cells, such as cancer cells. This helps to stop the cancer growing.
G-CSF is a type of growth factor. Growth factors are proteins made naturally in the body. One of the things they do is make the produce G-CSF is a man made (synthetic) version of these proteins. It’s a type of growth factor that makes the bone marrow produce more white blood cells. This can reduce the risk of infection after FLAG treatment.
You have fludarabine, cytarabine and idarubicin as a drip into your bloodstream (intravenously). You have G-CSF as an injection under the skin.
You might have treatment through a long plastic tube that goes into a large vein in your chest. The tube stays in place throughout the course of treatment. This can be a:
central line
PICC line
portacath
You might have treatment through a thin short tube (a cannula) that goes into a vein in your arm. You have a new cannula each time you have treatment.
When you are having this treatment through a cannula it could damage the tissue if it leaks out of the vein. This is called extravasation. This can happen anywhere along the vein that the drug is going into. It doesn’t happen very often. Tell your nurse straight away if you notice any changes such as swelling, redness, pain, burning, or a stinging feeling.
Your nurse will stop the drug treatment. And they will treat the area to relieve symptoms and reduce tissue damage. Contact your healthcare team if you develop any of these symptoms when you are at home.
You usually have injections under the skin (subcutaneous injection) into the stomach, thigh or top of your arm.
You might have stinging or a dull ache for a short time after this type of injection, but they don't usually hurt much. The skin in the area may go red and itchy for a while.
You usually have FLAG-Ida as a course of several cycles of treatment. A cycle of treatment means that you have these drugs and then have a rest to allow your body to recover.
Each cycle of treatment lasts about 28 days (4 weeks). You may start your next cycle the following day. Or you may need to wait until your blood counts have recovered. This can vary from person to person.
You might have up to 2 cycles of FLAG-Ida. You usually have each cycle of treatment in the following way:
You have G-CSF as an injection under the skin.
You have fludarabine as a drip into your bloodstream over 30 minutes.
You have cytarabine as a drip into your bloodstream over 4 hours.
You have G-CSF as an injection under the skin.
You have fludarabine as a drip into your bloodstream over 30 minutes.
You have cytarabine as a drip into your bloodstream over 4 hours.
You have idarubicin as a drip into your bloodstream over 5 to 10 minutes.
You have G-CSF as an injection under the skin.
You have G-CSF as an injection under the skin.
You have no treatment.
Once your blood count has recovered you start your second cycle of FLAG-Ida.
You have blood tests before and during your treatment. They check your levels of blood cells and other substances in the blood. They also check how well your liver and kidneys are working.
Before treatment starts you may have a blood test to check for viruses such as hepatitis B, hepatitis C, and HIV. This is called a viral screen.
It’s important for your doctor to know if you have had any of these viruses. This is because this treatment can weaken your and can cause the virus to become active again (reactivation).
Side effects can vary from person to person. They also depend on what other treatments you're having.
Your doctor, nurse or pharmacist will go through the possible side effects. They will monitor you during treatment and check how you are at your appointments. Contact your advice line as soon as possible if:
you have severe side effects
your side effects aren’t getting any better
your side effects are getting worse
Early treatment can help manage side effects better.
We haven't listed all the side effects here. Talk to your healthcare team if you have any new symptoms that you think might be a side effect of your treatment.
Remember it is very unlikely that you will have all of these side effects. But you might have some of them at the same time.
These side effects happen in more than 10 in 100 people (more than 10%). You might have one or more of them. They include:
Increased risk of getting an infection is due to a drop in white blood cells. Symptoms include a change in temperature, aching muscles, cough, headaches, feeling cold and shivery, pain or a burning feeling when peeing, or generally feeling unwell. You might have other symptoms depending on where the infection is.
Infections can sometimes be life threatening. You should contact your advice line urgently if you think you have an infection.
Sepsis happens when your body has an overwhelming response to an infection. Symptoms can include feeling very unwell, not passing urine, slurred speech or confusion, breathlessness, mottled or discoloured skin, extreme shivering or muscle pain.
You might be breathless and look pale due to a drop in red blood cells. This is called anaemia.
This is due to a drop in the number of platelets in your blood. These blood cells help the blood to clot when we cut ourselves. You may have nosebleeds or bleeding gums after brushing your teeth. Or you may have lots of tiny red spots or bruises on your arms or legs. This is known as petechiae.
This treatment can commonly cause lung problems such as a cough, breathlessness, or taking shallow breaths. This could be due to an infection, such as pneumonia or fluid in your lungs, stopping them from expanding fully.
Some people might have symptoms that include fast and shallow breathing, tiredness, drowsiness, confusion, feeling like you will faint and shortness of breath. This is called acute respiratory distress syndrome (ARDS). It causes lack of oxygen to your organs such as the lungs, heart and brain.
Other less common lung problems include changes to the lung tissue, making it less flexible or inflammation of the lungs (pneumonitis), or you might have scarring (pulmonary fibrosis).
Mouth sores and ulcers can be painful. It helps to keep your mouth and teeth clean, drink plenty of fluids and avoid acidic foods such as lemons. Chewing gum can help to keep your mouth moist. Tell your doctor or nurse if you have ulcers.
Contact your advice line if you have diarrhoea. For example, in one day you have 2 or more loose bowel movements than usual. If you have a , you might have more output than normal. Your doctor may give you anti diarrhoea medicine to take home with you after treatment.
Try to eat small meals and snacks regularly. It’s best to try to have a healthy balanced diet if you can. You don’t necessarily need to stop eating foods that contain fibre. But if your diet is normally very high in fibre, it might help to cut back on high fibre foods such as beans, nuts, seeds, dried fruit, bran and raw vegetables.
Drink plenty to try and replace the fluid lost. Aim for 8 to 10 glasses per day.
Feeling or being sick is usually well controlled with anti sickness medicines. It might help to avoid fatty or fried foods, eat small meals and snacks and take regular sips of water. Relaxation techniques might also help.
It is important to take anti sickness medicines as prescribed even if you don’t feel sick. It is easier to prevent sickness rather than treat it once it has started.
You might lose your appetite for various reasons while having cancer treatment. Sickness, taste changes or tiredness can put you off food and drinks.
You might experience pain in your tummy, bones or muscles. Speak to your doctor as they can prescribe medicine to help.
Talk to the team looking after you about this. They might be able to give you medicines or creams to help with this.
You might have liver changes that are usually mild and unlikely to cause symptoms. They usually go back to normal when treatment finishes.
You have regular blood tests to check for any changes in the way your liver is working.
You might notice skin changes, such as dryness, itching, freckles and rashes similar to acne on your face, neck and trunk.
Occasionally you may have other symptoms such as peeling of the skin or ulcers. If you have had previous radiotherapy treatment these areas might be sensitive.
Very rarely this treatment can cause darkening of the skin or a severe skin reaction that may start as tender red patches which leads to peeling or blistering of the skin. You might also feel feverish and your eyes may be more sensitive to light. This is serious and could be life threatening.
Tell your healthcare team if you have any skin changes. They might be able to prescribe medicine or advise on creams and lotions to use.
You might get a high temperature. Or you might feel cold or start shivering (chills).
Cytarabine syndrome sometimes happens about 6 to 12 hours after having this drug.
It causes a combination of symptoms. These include a high temperature, aching muscles, bone pain, occasionally chest pain, a rash, sore eyes, and extreme weakness. Steroids can help to prevent or treat this syndrome.
Cytarabine can cause abnormal results. Your doctor or nurse might need to take more biopsies or blood tests. Your healthcare team can explain this to you more.
You might feel very tired or find you are falling asleep during the day. Do not drive or operate machinery if you feel very sleepy.
Occasionally you may have problems getting to sleep or staying asleep (insomnia).
Let your doctor know straight away if you are very sleepy.
You might have problems with your movement and speech. This might be because of weakness in the muscles used for speech. You might be unsteady when you stand and find it difficult to walk. You might lose muscle control causing coordination problems.
You might feel very tired and as though you lack energy.
Various things can help you to reduce tiredness and cope with it, for example exercise. Some research has shown that taking gentle exercise can give you more energy. It is important to balance exercise with resting.
You might have eye problems including eye pain, blurred vision, loss of vision, sore, red, itchy, dry eyes (conjunctivitis) or an infection.
You have steroid eye drops to try and prevent conjunctivitis during treatment with high dose cytarabine. Your healthcare team can explain more.
Tell your healthcare team if you have any eye problems.
Let your doctor or nurse know if you have headaches. They can give you painkillers such as paracetamol to help.
This won't harm you. It’s due to the colour of idarubicin and lasts for one or two days.
These side effects happen in between 1 and 10 out of every 100 people (between 1% and 10%). You might have one or more of them. They include:
blood cancers such as
numbness or tingling in fingers or toes (peripheral neuropathy)
fluid build up in different parts of the body (oedema)
generally feeling unwell
inflammation and decreased blood supply to the bowel, this can be very serious. Symptoms might include passing blood from your bottom, feeling or being sick, constipation, diarrhoea or swelling of your tummy
enlarged - this might cause tummy pain
high levels of an in your blood that can be a sign of injury to your body’s tissues – you have regular blood tests to check this
feeling dizzy
high or low blood pressure – you might have headaches or feel faint
loss of sensation or touch causing tingling and numbness
muscle spasms
pain or difficulty passing urine
chest pain
a reaction to G-CSF – you might get a rash, shortness of breath, redness or swelling of the face and dizziness – some reactions can be life threatening, alert your nurse or doctor if notice any of these symptoms
heart problems such as irregular heartbeat or heart failure. Symptoms of heart failure include breathlessness, feeling tired, weakness, swelling in your legs and ankles, feeling faint or lightheaded. This treatment can also cause long term disease of the heart muscle (cardiomyopathy) - this can be life threatening
blood in your poo due to inflammation of your - contact your healthcare team straight away if you have any unexpected bleeding
These side effects happen in fewer than 1 in 100 people (less than 1%). You might have one or more of them. They include:
a disorder where the body attacks its own blood cells (an autoimmune disorder) such as autoimmune haemolytic anaemia, acquired haemophilia, or pemphigus
changes to the levels of chemicals in your blood due to the breakdown of tumour cells (tumour lysis syndrome) - you have regular blood tests to check for this
feeling confused
abnormal levels of pancreatic enzymes that are usually picked up in blood tests
bleeding in your stomach or gut, symptoms include passing black or tarry poo, stomach cramps, being sick (vomiting) blood, dark or bright red blood in your poo, looking pale, or feeling faint
being in a coma, this means that you cannot be woken
fits (seizures)
heart problems such as irregular heartbeat or heart failure. Symptoms of heart failure include breathlessness, tired, weakness, swelling in your legs and ankles, feeling faint or lightheaded
skin cancer
high uric acid levels in the blood that may cause gout – you have regular blood tests to check this
thinning of the bones which can make the bones weaker and easier to break (osteoporosis)
leaking of fluid and proteins out of the blood vessels into the tissues (capillary leak syndrome)
plum coloured, raised, painful sores on your legs or arms and sometimes the face and neck with a high temperature (Sweets syndrome)
lack of fluid in the body (dehydration)
shock, this can be life threatening. Some of the signs include looking pale, cold, clammy skin, sweating, fast shallow breathing, feeling or being sick. Contact your healthcare team immediately
bleeding in the brain
There isn't enough information to work out how often these side effects might happen. You might have one or more of them. They include:
an allergic reaction which might lead to swelling in areas such as the hands, feet, lips, tongue, around the eyes or genitals (allergic oedema)
personality changes
inflammation of your pancreas – symptoms include severe tummy pain, feeling or being sick, a high temperature or you may have loose poo
your nails may darken
We have more information about side effects and tips on how to cope with them.
Read more about how to cope with side effects
Cancer drugs can interact with medicines, herbal products, and some food and drinks. We are unable to list all the possible interactions that may happen. An example is grapefruit or grapefruit juice which can increase the side effects of certain drugs.
Tell your healthcare team about any medicines you are taking. This includes vitamins, herbal supplements and over the counter remedies. Also let them know about any other medical conditions or allergies you may have.
After having this treatment you should only have blood or platelets that are first treated with radiation (irradiated). The radiation lowers the risk of a reaction between your blood cells and the cells in the transfusion. No harm comes from having the irradiated blood.
In your medical records there is a note saying you should only have irradiated blood. You have a card to carry with this information. This is in case you need treatment at another hospital.
This treatment may harm a baby developing in the womb. It is important not to become pregnant or get someone pregnant while you're having treatment. Women must not become pregnant for about 7 months after the end of treatment. Men should not get someone pregnant for at least 6 months after treatment.
Talk to your doctor or nurse about effective contraception before starting treatment. Let them know straight away if you or your partner become pregnant while having treatment.
You may not be able to become pregnant or get someone pregnant after treatment with these drugs. Talk to your doctor before starting treatment if you think you may want to have a baby in the future.
Men might be able to store sperm before starting treatment. And women might be able to store eggs or ovarian tissue. But these services are not available in every hospital, so you would need to ask your doctor about this.
It is not known whether these drugs come through into the breast milk. Doctors usually advise that you don’t breastfeed during this treatment.
If you are having tests or treatment for anything else, always mention your cancer treatment. For example, if you are visiting your dentist.
Don’t have immunisations with live vaccines while you’re having treatment and for up to 12 months afterwards. The length of time depends on the treatment you are having.
Ask your doctor or pharmacist how long you should avoid live vaccinations.
In the UK, live vaccines include rubella, mumps, measles, BCG, and yellow fever.
You can usually have:
other vaccines, but they might not give you as much protection as usual
the flu vaccine (as an injection)
the coronavirus (COVID-19) vaccine
Talk to your doctor or pharmacist about the best time to have a vaccine in relation to your cancer treatment.
You can be in contact with other people who have had live vaccines as injections. If someone has had a live vaccine by mouth or nasal spray there may be a small risk the vaccine virus can be passed onto you if your is weakened.
Your healthcare team will let you know if you need to take any precautions if you are in close contact with someone who has had a live vaccine.
Read more about immunisations and cancer treatment
For further information about each drug and the possible side effects go to the electronic Medicines Compendium (eMC) website. You can find patient information leaflets for each drug on this website.
You can report any side effect you have to the Medicines and Healthcare Regulatory Agency (MHRA) as part of their Yellow Card Scheme.
Last reviewed: 16 Apr 2024
Next review due: 16 Apr 2027
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