Skip to content
RX Fast RX
RX Fast RX

  • Home
  • Privacy Policy
  • Contact us
  • DMCA
  • Terms and Conditions
    • Disclaimer
  • About Us
RX Fast RX

January 16, 2023

COVID-19 Treatments and Therapeutics – HHS.gov

HHS > Coronavirus > COVID-19 Treatments and Therapeutics
Blue information icon  COVID-19 services are available to individuals regardless of insurance or immigration status.
Treatments for COVID-19 are now widely available. If you test positive and are an older adult or someone who is at high risk of getting very sick from COVID-19, treatment may be available. Contact a healthcare provider right away after a positive test to determine if you are eligible, even if your symptoms are mild right now.
Talk to a healthcare professional about treatment options before taking medicine. People have been seriously harmed and even died after taking products not approved for COVID-19, even products approved or prescribed for other uses.
There are now locations where you can get tested and, if you test positive for COVID-19, you may also be eligible to receive treatment. If you test positive at a different location or with an at-home test, you can also go to these Test-to-Treat locations to receive a prescription from a qualified health care provider and treatment on the spot if eligible. Some Test-to-Treat sites also have telehealth options available.
Find a test-to-treat location
If you are sick with COVID-19 or think you might have COVID-19, follow these steps to care for yourself and to help protect other people in your home and community.
Clinical trials help researchers find better vaccines and medicines for COVID-19. Choosing to join a clinical trial is a personal decision. Talk with your doctor about participating in a clinical trial.
The FDA authorized two antivirals, Pfizer’s Paxlovid and Merck’s molnupiravir, for the treatment of COVID-19 in certain patients.
There are treatments for hospitalized patients with severe cases of COVID-19 that have been approved or authorized for emergency use by the Food and Drug Administration (FDA).
After a public health emergency was declared for the COVID-19 pandemic, it was determined that the Food and Drug Administration (FDA) could authorize the emergency use of tests, treatments, and vaccines to reduce suffering, loss of life and restore the health and security of our country.
Do you know the difference between FDA approval and authorization?
An approval of a new drug requires substantial scientific evidence of the effectiveness of the product and a demonstration of safety for the drug’s intended use(s). To determine an emergency use authorization (EUA), the FDA evaluates the totality of available scientific evidence and carefully balances any known or potential risks with any known or potential benefits of the product for use during an emergency.
>> Watch What is an EUA? video
Visit the HHS Facebook account Visit the HHS Twitter account Visit the HHS Instagram account
Visit the HHS YouTube account Visit the HHS Flickr account Visit the HHS LinkedIn account
Receive the latest updates from the Secretary, Blogs, and News Releases.
U.S. Department of Health & Human Services
200 Independence Avenue, S.W.
Washington, D.C. 20201
Toll Free Call Center: 1-877-696-6775​

source

rx

Post navigation

Previous post
Next post

Leave a Reply Cancel reply

Your email address will not be published. Required fields are marked *

Recent Posts

  • Jeremy Renner shares an update from a hospital bed after accident – USA TODAY
  • Concurrent Typhoid Fever and Dengue Hemorrhagic Fever: A Case … – Cureus
  • Human Papillomavirus Vaccine in Patients With Palmoplantar Warts – Dermatology Advisor
  • How Yellow Fever Intensified Racial Inequality in 19th-Century New … – Smithsonian Magazine
  • Jeremy Renner shares hospital bed photo following snowplow … – CBS News

Recent Comments

No comments to show.

Archives

  • February 2023
  • January 2023

Categories

  • Health
  • rx
©2023 RX Fast RX | WordPress Theme by SuperbThemes