Active Infection

Quest Diagnostics

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COVID-19

Quest Diagnostics

Active infection swab test

Active Infection Swab Illustration

This type of test helps to diagnose whether you currently have an active COVID-19 infection. A diagnosis can guide you and your doctor or healthcare provider to make an informed decision about self-isolating to protect your family and friends.

Who can get tested: Active infection testing may be right for you if you are currently experiencing COVID-19 symptoms or were exposed to the virus in the last 14 days. Common COVID-19 symptoms include fever, cough, and shortness of breath.

How the test works: Your doctor or healthcare provider will collect a specimen through a nasal or throat swab. The specimen is then sent to Quest laboratories for processing using either our lab-developed test, a Roche-developed test, or a Hologic-developed test.

Where to get tested: Contact your doctor or healthcare provider for guidance on where in your community to get tested for an active infection. (Do not go to a Quest patient service center for this test.) You may also consider finding a testing location through national partnerships we have with Walmart, CVS Health or find local testing options through Google.

 

Getting test results through MyQuest

Confirm that the healthcare provider who collects your COVID-19 specimen is sending it to Quest for processing. If so, your test results can be sent to you automatically through the secure MyQuest™ online portal. This is usually the quickest way to get results.

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COVID-19 testing statements

  • The antibody tests and the molecular tests (together “All tests”) have not been FDA cleared or approved;
  • All tests have been authorized by FDA under EUAs for use by authorized laboratories;
  • The antibody tests have been authorized only for the detection of IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens;
  • The molecular tests have been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses, pathogens; and,
  • All tests are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.