IVAC - Macmillan Cancer Support (2024)

Common side effects

Risk of infection

This treatment can reduce the number of white blood cells in your blood. These cells fight infection. If the number of white blood cells is low, you are more likely to get an infection. A low white blood cell count is sometimes called neutropenia.

Your doctor may give you antibiotics and other drugs to try to stop you getting an infection. These are called prophylactic medicines.

An infection can be very serious when the number of white blood cells is low. It is important to get any infection treated as soon as possible. Contact the hospital straight away on the 24-hour contact number you have been given if:

  • your temperature goes over 37.5°C (99.5°F)
  • you suddenly feel unwell, even with a normal temperature
  • you have symptoms of an infection
  • your temperature goes below 36°C (96.8°F).

Symptoms of an infection include:

  • feeling shivery and shaking
  • a sore throat
  • a cough
  • breathlessness
  • diarrhoea
  • needing to pass urine (pee) a lot, or discomfort when you pass urine.

It is important to follow any specific advice your cancer treatment team gives you.

The number of white blood cells will usually return to normal before your next treatment. You will have a blood test before having more treatment. If your white blood cell count is low, your doctor may delay your treatment for a short time, until your cell count increases.

You may be given a drug called G-CSF. This encourages the body to make more white blood cells. You have it as a small injection under the skin.

Bruising and bleeding

This treatment can reduce the number of platelets in your blood. Platelets are cells that help the blood to clot.

If the number of platelets is low, you may bruise or bleed easily. You may have:

  • nosebleeds
  • bleeding gums
  • heavy periods
  • blood in your urine (pee) or stools (poo)
  • tiny red, brown or purple spots that may look like a rash – these spots can be harder to see if you have black or brown skin.

If you have any unexplained bruising or bleeding, contact the hospital straight away on the 24-hour number. You may need a drip to give you extra platelets. This is called a platelet transfusion.

Anaemia (low number of red blood cells)

This treatment can reduce the number of red blood cells in your blood. Red blood cells carry oxygen around the body. If the number of red blood cells is low, this is called anaemia. You may feel:

  • very low in energy
  • breathless
  • dizzy and light-headed.

If you have these symptoms, contact the hospital straight away on the 24-hour number. You may need treatment for anaemia. If you are very anaemic, you may need a drip to give you extra red blood cells. This is called a blood transfusion.

Feeling sick

The nurses will give you anti-sickness drugs regularly. This will help prevent or control sickness during your treatment in hospital.If you feel sick or are sick (vomit), tell your nurse or doctor straight away. They can change the anti-sickness treatment. Or they might change the way you have it to something that works better for you.

Sore mouth and throat

This treatment may cause a sore mouth and throat. You may also get mouth ulcers. This can make you more likely to get a mouth or throat infection. Use a soft toothbrush to clean your teeth or dentures in the morning, at night and after meals.

Contact the hospital straight away on the 24-hour number, if:

  • a sore mouth or throat affects how much you can drink or eat
  • your mouth, tongue, throat or lips have any blisters, ulcers or white patches.

They can give you advice, and mouthwash or medicines to help with the pain or to treat any infection. Follow their advice and make sure you:

  • drink plenty of fluids
  • avoid alcohol and tobacco
  • avoid food or drinks that irritate your mouth and throat.

Constipation

This treatment can cause constipation. Constipation means that you are not able to pass stools (poo) as often as you normally do. It can become difficult or painful. Here are some tips that may help:

  • Drink at least 2 litres (3½ pints) of fluids each day.
  • Eat high-fibre foods, such as fruit, vegetables and wholemeal bread.
  • Do regular gentle exercise, like going for short walks.

If you have constipation, contact the hospital on the 24-hour number for advice. They can give you drugs called laxatives to help.

If you have not been able to pass stools for over 2 days and are being sick, contact the 24-hour number straight away.

Diarrhoea

This treatment may cause diarrhoea. Diarrhoea means passing more stools (poo) than is normal for you, or having watery or loose stools. You may also have stomach cramps. If you have a stoma, it may be more active than usual.

If you are passing loose stools 3 or more times a day and this is not normal for you, contact the hospital as soon as possible on the 24-hour number. Follow the advice they give you about:

  • taking anti-diarrhoea medicines
  • drinking enough fluids to keep you hydrated and to replace lost salts and minerals
  • any changes to your diet that might help.

They might also ask you for a specimen of your stool to check for infection.

Tummy pain

You may get pain in your tummy (abdomen), or have indigestion. Your doctor, nurse or pharmacist can give you advice or treatment to help. Contact the hospital straight away on the 24-hour number if your symptoms do not go away, or get worse.

Bladder irritation

Ifosfamide may irritate your bladder and cause discomfort or bleeding when you pass urine (pee). You will usually be given fluids through a drip (infusion) and a drug calledmesna (Uromitexan®)as an infusion or tablets or both. This helps to protect your bladder.

Your nurse usually tests your urine regularly whilst on IVAC. This is to make sure your bladder has not become irritated by the chemotherapy.

Make sure you drink at least 2 litres (3½ pints) of fluid during the 24 hours following chemotherapy. It is also important to empty your bladder regularly and to try to pass urine as soon as you feel the need to go.

Contact the hospital straight away if you feel any discomfort or stinging when you pass urine, or if you notice any blood in it.

Effects on the kidneys

This treatment can affect how the kidneys work. This is usually mild and goes back to normal after treatment ends. You will have blood tests to check how well your kidneys are working. Contact the hospital on the 24-hour number if you:

  • have blood in your urine (pee)
  • are passing less urine or peeing less often than usual.

Drinking fluids helps protect your kidneys. The advice is usually to try to drink at least 2 litres (3½ pints) of fluid each day. But follow any advice from your doctor, nurse or pharmacist about how much is right for you.

Hair loss

Your hair will get thinner. Or you may lose all the hair from your head. You may also lose your eyelashes and eyebrows, as well as other body hair. Hair loss usually starts after your first or second treatment.

If you want to cover up hair loss, there are different ways you can do this. Your nurse will give you information about coping with hair loss.

Remember to protect your skin from the sun. Use suncream with a sun protection factor (SPF) of at least 30 on your scalp. Or cover up with a hat or scarf.

Hair loss is almost always temporary. Your hair will usually grow back after treatment ends.

Tumour lysis syndrome (TLS)

Some people are at risk of developing a condition called tumour lysis syndrome (TLS) during this treatment. When treatment makes large numbers of cancer cells die and break down quickly, they release lots of waste products into the blood. This can affect how well the kidneys work. It may also cause problems with the heart rhythm.

TLS can be prevented. You will have regular blood tests to check for TLS. If you are at risk of TLS, you may have:

  • extra fluids through a drip
  • medicines such as rasburicasethrough a drip, or allopurinol as tablets.

Drinking at least 2 litres (3½ pints) of fluid a day will also help.

Skin changes

Chemotherapy can affect your skin. If your skin feels dry, try using soap-free cleansers and unperfumed moisturising cream every day.

This treatment can also:

  • cause a rash, which may be itchy
  • make your skin darker in some areas
  • make any area treated with radiotherapy become red or sore. If you have white skin the area will become red and if you have black or brown skin the area might become darker.
  • make you more sensitive to the sun.

Your skin may burn more easily during treatment and for several months after. Use a sun cream of at least SPF 30. SPF stands for sun protection factor. Cover up with clothing and wear a hat.

Always tell your doctor, nurse or pharmacist about any skin changes. They can give you advice or prescribe creams or medicines to help. Changes to your skin are usually temporary and improve when treatment ends.

Eye problems

This treatment can cause eye problems. Your doctor, nurse or pharmacist may give you eye drops to prevent or manage any problems. They will advise you how to use them.

If you usually wear contact lenses, your doctor, nurse or pharmacist can advise you about when you should not wear them.

It is important to always follow any eye care advice from your doctor, nurse or pharmacist.

Tell your doctor or nurse straight away if:

  • your eyes are watery, red or sore
  • you notice any changes in your eyesight.

Effects on the heart

This treatment can affect how the heart works. You may have teststo check how well your heart is working. These may be done before, during and after treatment.

If the treatment is causing heart problems, your doctor may change the type of treatment you are having.

Contact the hospital straight away on the 24-hour number if you have any of these symptoms during or after treatment:

  • breathlessness
  • dizziness
  • changes to your heartbeat
  • swollen feet and ankles.

Other conditions can cause these symptoms, but it is important to get them checked by a doctor.

Always call 999 if you have:

  • chest pain, pressure, heaviness, tightness or squeezing across the chest
  • difficulty breathing.

Feeling tired (fatigue)

This treatment can make you feel very tiredand you will need a lot of rest. You may get tired easily for some months after treatment ends. Gentle exercise, like short walks, can help you feel less tired. The tiredness will slowly get better.

If you feel sleepy, do not drive or use machinery.

IVAC - Macmillan Cancer Support (2024)

FAQs

What does Macmillan Cancer Support offer? ›

We provide services for people living with cancer at every stage of their cancer experience. We are here to provide emotional, practical, physical, and financial support.

How do I contact Macmillan Cancer Support? ›

If you have a question about cancer, please call our cancer support specialists free* on 0808 808 00 00 (7 days a week, 8am-8pm) or email our Support Line. If you wish to donate or talk to us about fundraising fill out the online fundraising form.

What is the red card for cancer patients? ›

If you are unwell, show it to the receptionist at your GP or A&E and to any healthcare professional you meet, including ambulance staff. This card will make sure you are seen immediately if needed. You have been given this card because your anti-cancer treatment can cause serious, life-threatening side effects.

Where does the money go for Macmillan Cancer Support? ›

Nearly 98% of our income is from voluntary donations, and this goes to provide our full range of services, from specialist cancer nurses to information booklets and support groups.

What are cancer patients entitled to? ›

Help with health costs

If you need special equipment or aids to help you live at home, you may be able to get what you need for free. Your doctor or nurse may arrange for this to be provided, or they can refer you to a social worker. If you pay for your own nursing home charges, you may be entitled to financial help.

Do all cancer patients get a Macmillan nurse? ›

You are usually referred to a CNS when you are first going for tests for cancer, or have just been diagnosed with cancer. They will give you a telephone number so you can contact them. But there may not always be a CNS for your type of cancer. You can ask your doctor if there is a nurse specialist you can talk to.

Can you self refer to Macmillan? ›

Or you can refer yourself. You will have a needs assessment before any care is arranged. A social worker will ask you about your daily routine and what you find difficult.

Is Macmillan palliative care? ›

Palliative care nurses are sometimes called Macmillan nurses. But not all Macmillan nurses specialise in palliative care. Palliative care nurses are experts in managing pain and other symptoms. For example, they can advise you about pain medicines if your pain is not well managed.

What is a macmillan buddy? ›

If you need to talk, we're here to listen. With a weekly call or visit from one of our trained Macmillan Buddies, you don't have to face cancer alone. Sign up for support from a Macmillan Buddy. Get up to 12 weeks of support for you or someone else.

What do cancer patients have to pay for? ›

Some people receive treatment far from home. In this case, you may need to pay for lodging, meals, and other related travel expenses. Family and living expenses. These include costs of household upkeep and family care during cancer treatment.

What do cancer patients qualify for? ›

Social Security Disability Insurance for People with Cancer. Social Security Disability Insurance (SSDI) is a federal benefit for people who have disabilities that keep them from working. To be able to get SSDI, people must have worked in jobs where they paid into Social Security.

What is the cancer card? ›

So what is the cancer card? The “cancer card” is a term coined by those affected by cancer in some way, shape or form. The cancer card is kind of like a “get out of jail free” card in the game of Monopoly.

What does Macmillan Cancer Support provide? ›

Macmillan information and support centres support people affected by cancer. They are free to use and we have centres across the UK. Macmillan nurses are specialist cancer nurses who can help you to understand your cancer diagnosis and treatment options, and support you though your cancer experience.

What is the Macmillan recovery package? ›

The Recovery Package is a series of key interventions which, when delivered together, can greatly improve outcomes for people living with and beyond cancer.

How much of your donation goes to Macmillan? ›

St. John Ambulance: for every £1 spent, 87.3p goes on charitable activities, 10p is spent on fundraising, and 2.7p is spent on generating income. Macmillan Cancer Support: 73p charitable activities, 24.4p fundraising, and 2.6p generating income.

Does the government give you money if you have cancer? ›

Federal and state benefit programs offer help to meet health care and income needs. These programs can help those who can't work due to cancer, treatment or aftereffects.

What is a Macmillan care plan? ›

This Cancer Care Plan is where you can write down your priorities and concerns, and plan your next steps. The plan also includes information about local services and support and how Macmillan Cancer Support can help you.

How much does Macmillan Cancer Support raise? ›

We gave out over £19 million in Macmillan Grants and estimate that we helped to secure over £350 million in benefits through the advice provided by our Support Line and local Welfare Rights Services. Our supporters and fundraisers raised an incredible £221.2 million.

Top Articles
Latest Posts
Article information

Author: Gregorio Kreiger

Last Updated:

Views: 6453

Rating: 4.7 / 5 (57 voted)

Reviews: 80% of readers found this page helpful

Author information

Name: Gregorio Kreiger

Birthday: 1994-12-18

Address: 89212 Tracey Ramp, Sunside, MT 08453-0951

Phone: +9014805370218

Job: Customer Designer

Hobby: Mountain biking, Orienteering, Hiking, Sewing, Backpacking, Mushroom hunting, Backpacking

Introduction: My name is Gregorio Kreiger, I am a tender, brainy, enthusiastic, combative, agreeable, gentle, gentle person who loves writing and wants to share my knowledge and understanding with you.