Who can and cannot have sotrovimab
Who can have sotrovimab
Sotrovimab can be given to most adults, and children aged 12 years or older who weigh at least 40kg.
You may be eligible for sotrovimab if:
- you're in the highest risk group below
- you've tested positive for COVID-19 – find out about COVID-19 rapid lateral flow test
- you have had COVID-19 symptoms within the last 5 days
Show people at highest risk
You may be at highest risk of getting seriously ill from COVID-19 if you:
- have Down's syndrome, or another chromosomal condition that affects your immune system
- have certain types of cancer, or had treatment for certain types of cancer
- have sickle cell disease
- have certain conditions affecting your blood, including some types of blood cancer
- have chronic kidney disease (CKD) stage 4 or 5, including people on dialysis
- have severe liver disease
- have had an organ transplant or are on the organ transplant waiting list
- have certain autoimmune or inflammatory conditions, such as rheumatoid arthritis or inflammatory bowel disease
- have HIV or AIDS and have a weakened immune system
- have a condition affecting your immune system
- have a condition affecting the brain or nervous system, such as multiple sclerosis, muscular dystrophy, motor neurone disease, myasthenia gravis, Huntington's disease, Parkinson's disease or certain types of dementia
- have certain lung conditions or treatments for lung conditions
This list is a summary and does not cover everything.
If you're unsure if you are eligible, speak to your GP or hospital specialist who can advise you.
Find out more about people at the highest risk who are eligible for COVID-19 treatment on the National Institute for Health and Care Excellence (NICE) website
Who may not be able to have sotrovimab
Sotrovimab is not suitable for some people. To make sure it's safe for you, tell your doctor or nurse if:
- you have ever had an allergic reaction to sotrovimab
- you are pregnant, trying to get pregnant or breastfeeding
Page last reviewed: 20 December 2021
Next review due: 20 December 2024