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Test Name Result Flag Reference Range Lab: Patient Information

The document is a lab report for a COVID-19 test. It shows that the test for an 11-year-old female named Angelica Sofia Carmona Duran was negative for SARS-CoV-2. While the test result was negative, the report notes that false negatives are possible, especially without symptoms. It was performed by LabCorp and reviewed by her physician, Dr. Aigul Guilmanova.

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84 views

Test Name Result Flag Reference Range Lab: Patient Information

The document is a lab report for a COVID-19 test. It shows that the test for an 11-year-old female named Angelica Sofia Carmona Duran was negative for SARS-CoV-2. While the test result was negative, the report notes that false negatives are possible, especially without symptoms. It was performed by LabCorp and reviewed by her physician, Dr. Aigul Guilmanova.

Uploaded by

roxana
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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LabCorp PATIENT INFORMATION REPORT STATUS: FINAL

SPECIMEN INFORMATION Carmona Duran, Angelica Sofia


ORDERING PHYSICIAN
ACCOUNT NO: 10053251 DOB: December 03, 2010
Guilmanova, Aigul
SPECIMEN: 09156031490 AGE: 11
CLIENT INFORMATION
REQUISITION: 89652892 GENDER: Female
2021-12-22 20:07:00 -0700
Lab ref no: FASTING: Unknown
Walgreens COVID-19
PATIENT ID: 89652892
COLLECTED: 12/21/2021 08:00AM MDT
RECEIVED: 12/21/2021 Clinical Info:
REPORTED: 12/22/2021 10:07PM ET

Test Name Result Flag Reference Range Lab


SARS-CoV-2, NAA
SARS-CoV-2, NAA Not Detected NORMAL Not Detected 01
This nucleic acid amplification test was developed and its performance
characteristics determined by LabCorp Laboratories. Nucleic acid
amplification tests include RT-PCR and TMA. This test has not been
FDA cleared or approved. This test has been authorized by FDA under
an Emergency Use Authorization (EUA). This test is only authorized
for the duration of time the declaration that circumstances exist
justifying the authorization of the emergency use of in vitro
diagnostic tests for detection of SARS-CoV-2 virus and/or diagnosis
of COVID-19 infection under section 564(b)(1) of the Act, 21 U.S.C.
360bbb-3(b) (1), unless the authorization is terminated or revoked
sooner.
When diagnostic testing is negative, the possibility of a false
negative result should be considered in the context of a patient's
recent exposures and the presence of clinical signs and symptoms
consistent with COVID-19. An individual without symptoms of COVID-19
and who is not shedding SARS-CoV-2 virus would expect to have a
negative (not detected) result in this assay.
SARS-CoV-2, NAA 2 DAY TAT
SARS-CoV-2, NAA 2 DAY TAT Performed NORMAL 02

Performing Laboratory Information:

01: LabCorp RTP, 1912 TW Alexander Drive, RTP NC, 277090150, phone: 800-735-4087, Director: MDPhD
Anjen Chenn
02: LabCorp Birmingham, 1801 First Avenue South, Birmingham AL, 352331935, phone: 205-581-3500,
Director: MD Brian D Ragland

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