People at risk of severe COVID-19 to have access to antiviral Paxlovid
A further 1.4 million people who have an increased risk for progression to severe COVID-19 will be eligible for Paxlovid if they test positive.
NICE already recommends Paxlovid (also called nirmatrelvir plus ritonavir and made by Pfizer) for an estimated 3.9 million people who do not need supplemental oxygen for COVID-19 and who have an increased risk for progression to severe COVID-19. This includes people with certain cancers, people who have had haematological stem cell transplant or who have a haematological disease and people with liver or kidney disease (2).
Following a partial review NICE has published updated final draft guidance which increases the number of people eligible to access Paxlovid to an estimated 5.3 million. This means that within 3 months of NICE publishing final guidance, the following groups will also have access to Paxlovid if they test positive for Covid 19:
People aged 85 years and over.
People with end-stage heart failure who have a long-term ventricular assistance device.
People on the organ transplant waiting list.
People aged 70 years and over, or who have a BMI of 35 kg/m2 or more, diabetes or heart failure, and are resident in a care home, or are already hospitalised
Paxlovid is an antiviral medicine, given as 2 separate tablets to people within 5 days of getting COVID-19 symptoms. It works by stopping the virus from growing and spreading in the body. It’s 2 separate medicines, nirmatrelvir and ritonavir. Nirmatrelvir stops the virus from growing and spreading, and ritonavir helps nirmatrelvir from being broken down in the body while it is working.
People eligible for COVID-19 treatments can get free lateral flow tests from participating pharmacies and should take a test as soon as they have symptoms, even if mild. If positive, people should call their GP surgery, NHS 111 or hospital specialist as soon as possible.
Eligible patients can pick up free rapid lateral flow tests from a local participating pharmacy.