Patient NAME : Mr Akshay

DOB/Age/Gender : 24 Y 2 M 13 D/Male Report STATUS : Final Report

Patient ID / UHID : 11831851/OF11831851 Barcode NO : 15472677
Referred BY : Self Sample Type : Serum
....

Sample Collected : Mar 23, 2025, 02:03 PM Report Date : Mar 25, 2025, 01:40 PM.
Test Description Value(s) Unit(s) Reference Range

HIV Antibody, Rapid Card

HIV 1 & 2 ANTIBODIES NON REACTIVE - NON REACTIVE

Qualilative immunoassay,rapid card

Interpretation:
RESULTS REMARKS
Reactive A reactive test results indicates antibody detected against HIV-1/2
Non reactive A non reactive test results indicates antibody is not detected against HIV- 1/2.

NOTE :

1. This is only a screening test. All samples detected reactive must be confirmed by using HIV Western Blot. Therefore for a definitive diagnosis, the
patient’s clinical history, symptomatology as well as serological data, should be considered. The results should be reported only after complying with above
procedure.

2. Some samples show cross reactivity fir HIV antibodies.Following factors are found to cause false positive HIV antibody test results: naturally occurring
antibodies, Passive immunization, Leprosy, Renal Disorders, Tuberculosis, Myco-bacterium avium, Herpes simplex, Hypergammaglobulinemia, Malignant
neoplasms, Rheumatoid ar thritis, Tetanus vaccination, Autoimmune diseases, Blood Transfusion, Multiple myeloma, Haemophelia, Heat treated specimens,
Lipemic serum, Anti-nuclear antibodies, T-cell leukocyte antigen antibodies, Epstein Barr virus, HLA antibodies and other retroviruses.

3. False negative results may occur during the window period and during the end stage of the disease.

*** End Of Report ***

Booking Centre :- Kangoo CC, Village , Thana, Po- Kangoo, Distt- Hamirpur, Near New DAV School, Himachal Pradesh-
177040
Processing Lab :- Redcliffe Lifetech Pvt. Ltd., SCO 171, Sector 37-C, Chandigarh-160036

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 Terms and Conditions of Reporting

1. The presented findings in the Reports are intended solely for informational and interpretational purposes by the
referring physician or other qualified medical professionals possessing a comprehensive understanding of
reporting units, reference ranges, and technological limitations. The laboratory shall not be held liable for any
interpretation or misinterpretation of the results, nor for any consequential or incidental damages arising from
such interpretation.

2. It is to be presumed that the tests performed pertain to the specimen/sample attributed to the Customer's name
or identification. It is presumed that the verification particulars have been cleared out by the customer or his/her
representation at the point of generation of said specimen / sample. It is hereby clarified that the reports
furnished are restricted solely to the given specimen only.

3. It is to be noted that variations in results may occur between different laboratories and over time, even for the
same parameter for the same Customer. The assays are performed and conducted in accordance with standard
procedures, and the reported outcomes are contingent on the specific individual assay methods and equipment(s)
used, as well as the quality of the received specimen.

4. This report shall not be deemed valid or admissible for any medico-legal purposes.

5. The Customers assume full responsibility for apprising the Company of any factors that may impact the test
finding. These factors, among others, includes dietary intake, alcohol, or medication / drug(s) consumption, or
fasting. This list of factors is only representative and not exhaustive.
SMART HEALTH REPORT
RT

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