This is an official
CDC HEALTH ADVISORY
Distributed via the CDC Health Alert Network
May 24, 2022, 9:00 AM ET
CDCHAN-0467
COVID-19 Rebound After Paxlovid Treatment
Summary
The Centers for Disease Control and Prevention (CDC) is issuing this Health Alert Network (HAN) Health
Advisory to update healthcare providers, public health departments, and the public on the potential for
recurrence of COVID-19 or COVID-19 rebound. Paxlovid continues to be recommended for early-
stage treatment of mild to moderate COVID-19 among persons at high risk for progression to
severe disease. Paxlovid treatment helps prevent hospitalization and death due to COVID-19. COVID-19
rebound has been reported to occur between 2 and 8 days after initial recovery and is characterized by a
recurrence of COVID-19 symptoms or a new positive viral test after having tested negative. A brief
return of symptoms may be part of the natural history of SARS-CoV-2 (the virus that causes
COVID-19) infection in some persons, independent of treatment with Paxlovid and regardless of
vaccination status. Limited information currently available from case reports suggests that persons
treated with Paxlovid who experience COVID-19 rebound have had mild illness; there are no reports of
severe disease. There is currently no evidence that additional treatment is needed with Paxlovid or other
anti-SARS-CoV-2 therapies in cases where COVID-19 rebound is suspected.
Regardless of whether the patient has been treated with an antiviral agent, risk of transmission during
COVID-19 rebound can be managed by following CDC’s guidance on isolation, including taking other
precautions such as masking.
Staying up to date with COVID-19 vaccination lowers the risk of getting COVID-19 and helps prevent
serious outcomes of COVID-19, such as severe illness, hospitalization, and death.
Background
Paxlovid (nirmatrelvir tablets; ritonavir tablets) is a prescription oral antiviral drug that reduces the risk of
hospitalization and death for patients with mild-to-moderate COVID-19 who are at risk of disease
progression and severe illness (1). It is available under Emergency Use Authorization (EUA) by the U.S.
Food and Drug Administration (FDA) for adults and pediatric patients (12 years of age and older weighing
at least 40 kilograms or 88 pounds). Treatment should be initiated as soon as possible and within 5 days
of symptom onset among persons eligible to receive the treatment under the EUA who:
Test positive for SARS-CoV-2 infection;
Have mild to moderate illness;
Have one or more risk factors for progression to severe disease;
Do not require hospitalization due to severe or critical COVID-19 at the time of treatment
initiation; and
Do not have evidence of severe renal or hepatic impairment.
Recent case reports document that some patients with normal immune response who have completed a
5-day course of Paxlovid for laboratory-confirmed infection and have recovered can experience recurrent
illness 2 to 8 days later, including patients who have been vaccinated and/or boosted (were up to date
with COVID-19 vaccination) (2-4). These cases of COVID-19 rebound had negative test results after
Paxlovid treatment and had subsequent positive viral antigen and/or reverse transcriptase polymerase
chain reaction (RT-PCR) testing. Both the recurrence of illness and positive test results improved or
resolved (median of 3 days) without additional anti-COVID-19 treatment. Based on information from the
case reports, COVID-19 rebound did not represent reinfection with SARS-CoV-2 or the development of
resistance to Paxlovid; also, no other respiratory pathogens were identified among known cases. Possible
transmission of infection during COVID-19 rebound has been described (3); however, it remains unknown
whether the likelihood of transmission during rebound differs from the likelihood of transmission during
the initial infection.
In the Paxlovid clinical trial, a small number of participants had one or more positive SARS-CoV-2 RT-
PCR test results after testing negative, or an increase in the amount of SARS-CoV-2 detected by PCR,
after completing their treatment course (5). This finding was observed in persons administered Paxlovid
and in persons given placebo. There was no increased occurrence of hospitalization or death, and there
was no evidence that the rebound in detectable viral RNA was the result of SARS-CoV-2 resistance to
Paxlovid (5).
COVID-19 rebound is characterized by a recurrence of symptoms or a new positive viral test after having
tested negative. People with COVID-19 rebound should follow CDC recommendations regarding isolation
of infected patients regardless of treatment with an antiviral agent and/or previous isolation after the initial
infection. People with recurrence of COVID-19 symptoms or a new positive viral test after having tested
negative should restart isolation and isolate again for at least 5 days. Per CDC guidance, they can end
their re-isolation period after 5 full days if fever has resolved for 24 hours (without the use of fever-
reducing medication) and symptoms are improving. The individual should wear a mask for a total of 10
days after rebound symptoms started. Some people continue to test positive after day 10 but are
considerably less likely to shed infectious virus. Currently, there are no reports of severe disease among
persons with COVID-19 rebound. Paxlovid continues to be recommended for early-stage treatment of
mild to moderate COVID-19 among persons at high risk for progression to severe disease.
Recommendations for Healthcare Providers
For patients with COVID-19 rebound
There is currently no evidence that additional treatment for COVID-19 is needed for COVID-19
rebound. Based on data available at this time, patient monitoring continues to be the most
appropriate management for patients with recurrence of symptoms after completion of a
treatment course of Paxlovid.
Advise people with COVID-19 rebound to follow CDC’s guidance on isolation and take
precautions to prevent further transmission. Patients should re-isolate for at least 5 days. Per
CDC guidance, they can end their re-isolation period after 5 full days if fever has resolved for 24
hours (without the use of fever-reducing medication) and symptoms are improving. The patient
should wear a mask for a total of 10 days after rebound symptoms started.
Consider clinical evaluation of patients who have COVID-19 rebound and symptoms that persist
or worsen.
Healthcare providers are encouraged to report cases of COVID-19 rebound to Pfizer after
Paxlovid treatment using the following online tool: Pfizer Safety Reporting and to FDA MedWatch.
Complete and submit a MedWatch form, or complete and submit FDA Form 3500 (health
professional) by fax (1-800-FDA-0178). Call 1-800-FDA-1088 for questions.
For patients just diagnosed with COVID-19
Healthcare providers should counsel patients on available COVID-19 treatment options,
particularly for those patients at increased risk of developing severe COVID-19.
Paxlovid should be considered for any patient who meets the eligibility criteria. For information on
Paxlovid eligibility, refer to FDA’s Fact Sheet for Healthcare Providers.
Due to the potential for severe drug-drug interactions with the ritonavir component of Paxlovid, it
is strongly suggested that healthcare providers not experienced in prescribing this drug refer to
the Fact Sheet for Healthcare Providers, the Paxlovid Patient Eligibility Screening Checklist Tool
for Prescribers, and the NIH Statement on Paxlovid Drug-Drug Interactions | COVID-19
Treatment Guidelines. Healthcare providers can also contact a local clinical pharmacist or
infectious disease specialist for advice.
For further information on the use of Paxlovid, CDC recommends healthcare providers continue
to closely follow NIH’s COVID-19 Treatment Guidelines, the Assistant Secretary for
Preparedness and Response Public Health Emergency COVID-19 Therapeutics site, and IDSA’s
Guidelines on the Management of Patients with COVID-19.
Recommendations for Public Health Departments and Public Health Jurisdictions
State and local health departments should be aware of COVID-19 rebound and disseminate the
recommendations for healthcare providers and the public.
Health departments should communicate to individuals about measures to prevent further
transmission. The phenomenon of COVID-19 rebound reiterates the importance of following
CDC’s isolation guidance. Isolation should be restarted after the onset of rebound symptoms or a
positive test result. Per CDC guidance, people can end re-isolation after 5 full days with resolution
of their fever for 24 hours (without the use of fever-reducing medication) and if their symptoms
are improving. The individual should wear a mask for a total of 10 days after rebound symptoms
started.
Health departments should communicate ongoing and up to date information on therapeutics for
COVID-19 and their availability to healthcare providers within their jurisdiction.
Recommendations for the Public
You may be experiencing COVID-19 rebound if you have been diagnosed in the past 2 weeks
and have recovered from COVID-19 and then experience recurrent COVID-19 symptoms or
develop newly positive test results after recovery.
If you experience COVID-19 rebound, you should follow CDC’s isolation guidance. Isolate again
and restart the recommended 5-day isolation period at the time of recurrence of symptoms or a
new positive COVID-19 test result. You can end re-isolation after 5 days if you are fever-free for
24 hours without the use of fever-reducing medication and your symptoms are improving. You
should also wear a mask for 10 days after rebound.
Contact a healthcare provider if your COVID-19 rebound symptoms persist or worsen.
Consult with your healthcare provider if you have additional questions about your treatment.
You are encouraged to report a possible case of COVID-19 rebound after Paxlovid treatment to
Pfizer using the following online tool: Pfizer Safety Reporting.
For More Information
FDA Updates on Paxlovid for Health Care Providers | FDA
Paxlovid Patient Eligibility Screening Checklist Tool
FDA Paxlovid Emergency Use Authorization letter
COVID-19 Treatment Guidelines: What’s New
COVID-19 Treatment Guidelines: Antiviral Therapy
NIH Statement on Therapies for High-Risk, Nonhospitalized Patients | COVID-19 Treatment
Guidelines
NIH Statement on Paxlovid Drug-Drug Interactions | COVID-19 Treatment Guidelines
Pfizer Safety Reporting
References
1. Hammond J, Leister-Tebbe H, Gardner A, Abreu P, Bao W, Wisemandle W, et al. Oral
Nirmatrelvir for High-Risk, Nonhospitalized Adults with COVID-19. New Engl J Med 2022;
386(15): 1397-1408.
2. Gupta K, Strymish J, Stack G, Charness M. Rapid relapse of symptomatic omicron SARS CoV-2
infection following early suppression with nirmatrelvir/ritonavir. 26 April 2022, PREPRINT (Version
1) available at Research Square [https://doi.org/10.21203/rs.3.rs-1588371/v1].
3. Charness M, Gupta K, Stack G, Strymish J, Adams E, Lindy D, Mohi H, Ho D. Rapid relapse of
symptomatic omicron SARS CoV-2 infection following early suppression with
nirmatrelvir/ritonavir. 13 May 2022, PREPRINT (Version 2) available at Research Square
[https://doi.org/10.21203/rs.3.rs-1588371/v2].
4. Carlin AF, Clark AE, Chaillon A, Garretson AF, Bray W, Porrachi M, et al. Virologic and
Immunologic Characterization of COVID-19 Recrudescence after Nirmatrelvir/Ritonavir
Treatment. 18 May 2022, PREPRINT (Version 1) available at Research Square
[https://doi.org/10.21203/rs.3.rs-1662783/v1].
5. Food and Drug Administration. FDA Updates on Paxlovid for Health Care Providers. Available at:
https://www.fda.gov/drugs/news-events-human-drugs/fda-updates-paxlovid-health-care-
providers. Accessed on May 12, 2022.
Categories of Health Alert Network messages:
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and local laboratory directors, public information officers, HAN coordinators, and clinician
organizations##