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FDA approval will allow Paxlovid to remain available for adults indefinitely. There are other therapies for COVID, and anyone cheapest lamisil cannot take Paxlovid—perhaps because it would interact with another medication—should talk to their doctor about the best approach for their situation. That means you must either be 50 or older age remains the strongest factor for severe COVID outcomes, according to the FDA, although, the agency still authorizes Paxlovid for adolescents and teenagers ages 12 and older who weigh at least 88 pounds.

We asked Yale Medicine infectious diseases experts common questions about Paxlovid. If you are pregnant or breastfeeding, the FDA recommends discussing your options and specific situation with your health care provider, since there is no experience using the drug in these populations. When it approved Paxlovid in May, the FDA said there not a clear association between Paxlovid treatment and COVID rebound based on available data, and rebound rates in clinical trials were similar among participants who took Paxlovid and those who took a placebo.

In June, the CDC released guidance for clinicians, saying a brief return of symptoms may be part of the natural history of SARS-CoV-2 infection in some people, independent of treatment with Paxlovid, adding that there is no evidence additional treatment is needed. Yale experts answer commonly asked questions about the oral antiviral medication. Topal says people also should remember that Paxlovid, even with its high efficacy, is not perfect, and even if it were, viruses can mutate and develop resistance to antiviral medications.

Paxlovid also decreases the metabolism of anticoagulants, or blood thinners, that many older adults depend on, driving up levels of those medications in the body to a point where they are unsafe, Dr. Anyone who has Human Immunodeficiency Virus 1 HIV-1 infection should talk to their health care provider before taking Paxlovid, since it may lead to some HIV-1 medicines not working as well in the future. But because many children reach 88 pounds—considered to be an adult weight—the FDA has allowed extensions of EUAs for medications such as monoclonal antibodies and remdesivir in younger age groups, adds Dr.

Roberts says Paxlovid should work against the Omicron subvariant EG. The most common side effects of taking Paxlovid include impaired sense of taste for example, a metallic taste in the mouth and diarrhea, according to the FDA. Most people who take Paxlovid should not experience serious side effects, explains Dr. Since Paxlovid is cleared by the kidneys, dose adjustments may be required for patients with mild-to-moderate kidney disease, explains Dr.

The FDA has provided a fact sheet on Paxlovid with a full list of known side effects. The CDC says a rebound does not mean a person was resistant to Paxlovid, nor does it mean they were reinfected with the virus. Paxlovid is an oral antiviral pill that can be taken at home to help keep high-risk patients from getting so sick that they need to be hospitalized. Scientists are studying the effects of longer treatment durations, longer periods of isolation, and other ways of managing the problem, he adds.

So, if you are eligible to take the pills, you can take them at home and lower your risk of going to the hospital. However, scientists are still studying the Paxlovid rebound. Always seek the individual advice of your health care provider with any questions you have regarding a medical condition. You have to take Paxlovid within five days of developing symptoms.

Paxlovid also interacts with common medications, including cholesterol-lowering statins like Lipitor. But in many cases, patients can talk to their doctors about taking a temporary break from some of those drugs while taking Paxlovid, he adds. You also qualify if you have certain underlying conditions including cancer, diabetes, obesity, or others. The drug also remains available to everyone 12 and older weighing at least 88 pounds who has mild-to-moderate disease and is at high risk for severe disease under an FDA Emergency Use Authorization.

When it applied for FDA authorization in, Pfizer presented data from a clinical trial conducted between mid-July and early December All of the trial participants were unvaccinated and they took the drug within three days of symptom onset.

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