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    Patient Name : Ms Chaya Vasantrao Chinde

    DOB/Age/Gender : 62 Y/Female Sample Collected : Jun 10, 2024, 07:33 AM


    Patient ID / UHID : 8567253/RCL7926286 Report Date : Jun 10, 2024, 04:03 PM.
    Referred By : Self Barcode No : SI515352
    ....

    Sample Type : Serum Report Status : Final Report


    Test Description Value(s) Unit(s) Reference Range

    Hepatitis B Surface Antigen (HBsAg), Rapid Card

    HEPATITIS B SURFACE ANTIGEN (HBsAg) NON REACTIVE NON REACTIVE


    Qualitative immunoassay,rapid card

    Interpretation:
    RESULTS REMARKS
    Reactive The sample is Reactive for HBsAg
    Non Reactive The sample is Non Reactive for HBsAg

    Note
    1.This is only a Screening test. All reactive results should be confirmed by confirmatory test. Therefore for a definitive diagnosis, the patient's
    clinical history ,symptomatalogy as well as serological data, should be considered. The results should be reported only after complying with
    above procedure.
    2. Additional follow up testing using available clinical methods (along with repeat HBsAg rapid card test) is required, if the test is Non reactive
    with persisting clinical symptoms
    3. False positive results may be observed in patients receiving mouse monoclonal antibodies, on heparin therapy, on biotin supplements for
    diagnosis or therapy, presence of heterophilic antibodies in serum or after HBV vaccination for transient period of time.
    4. False negative reaction may be due to processing of sample collected early in the course of disease or presence of mutant forms of HBsAg.

    *** End Of Report ***

    Booking Centre :- Home Collection


    Processing Lab :- Redcliffe Lifetech Pvt. Ltd., First Floor, B Wing. Aswani Chambers, S.No. 199+204+205 206/1, 209/1,
    Plot No. 45/B, Corresponding city, S.No 199 Village Lohgaon Pune 411014,

    Page 1 of 1
    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.

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