Published on Jun 08, 2022 | 2:56 PM
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As time passes and studies evaluating COVID progress, the healthcare community is continually keeping up with medical guidelines and regulations from the US Food and Drug Administration (FDA) for patients regarding safe treatment options and ways to minimize risks of severe COVID.
Recently, the FDA approved Paxlovid for the treatment of mild-to-moderate Covid-19 patients. While this has been approved, patients still must meet the following qualifications to get prescribed Paxlovid:
It is also regulated by the FDA that Paxlovid is not authorized for the following:
Clinical trials supported by the Emergency Use Authorization (EUA) have reported that those at high risk of severe COVID and treated with Paxlovid reduced hospitalization or death by 88%.
The FDA continues to study the results of clinical trials and make updates accordingly. As of today, Paxlovid is authorized for COVID-19 prescription treatment and has been shown to reduce hospitalization and deaths for individuals at high risk.
For individuals who qualify for Paxlovid treatment, please note the potential side effects:
To read more updates from the FDA on Paxlovid, click here.
To consult with a doctor to see if Paxlovid might be right for you, consult online with a Call-On-Doc provider here.
English graduate and Call-On-Doc’s medical resource guide, Wayne C. Hahne is an experienced and passionate medical education content expert. Through diligent research, provider interviews and utilizing the industry's leading resources for wellness information, it is Mr. Hahne’s personal mission to educate the general public on medical conditions with in-depth and easy-to-understand written guides.
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