Patient Name: Mrs.
VARSHARANI VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:41
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- BIOCHEMISTRY
Glucose, Random, Blood
Test Name Result Your Value Reference Range
Blood Glucose Random (RBS), mg/dL 82.03 Normal 70 - 140
[Method: Colorimetric End-Point]
Interpretation:
This test checks your blood glucose levels, at random time of the day.
Diagnosing Diabetes
RBS value Interpretation
70-140 mg/dL Normal
>/=200 Diabetic
The above reference ranges are as per ADA guidelines.
*** End Of Report ***
Barcode No : PPS0058950
Sample Type : FLUORIDE PLASMA (R)
Page 1 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:42
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- CLINICAL PATHOLOGY
Complete Urine Examination
Test Name Result Your Value Reference Range
Physical Examination
Volume, ml 30 Normal >1.5
Colour Pale Yellow
Transparency Slight Hazy Clear
Chemical Examination
pH 6.0 Normal 5.0 - 8.0
[Method: Manual]
Specific Gravity 1.010 Normal 1.001-1.030
[Method: Manual]
Protein Absent Negative
[Method: manual]
Glucose Absent Negative
[Method: Manual]
Blood Present(Trace) Negative
[Method: Manual]
Ketone Absent Negative
[Method: Manual]
Bilirubin Absent Negative
[Method: Manual]
Urobilinogen Normal Negative
[Method: Manual]
Nitrite Negative Negative
[Method: Manual]
Leucocyte Esterase Present (+) Absent
[Method: Manual]
Microscopic Examination
Barcode No : PPS0058951
Sample Type : URINE.
Page 2 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:42
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- CLINICAL PATHOLOGY
WBC/Pus Cells, /hpf 4-5 Normal 0-5
[Method: Microscopy]
Transitional/Squamous epithelial cells, 6-8 High 0-4
/hpf
[Method: Microscopy]
RBCs, /hpf occasional Normal 0-2
[Method: Microscopy]
Crystals CALCIUM OXALATE + Absent
[Method: Microscopy]
Casts Absent Absent
[Method: Microscopy]
Bacteria Absent
Interpretation:
Microscopic examination done on centrifuge urine, please note that grading of bacteria needs to be correlated with the culture in case found
significant clinically. The bacteria can also be a part of surrounding skin flora.
Protein: Protein excretion can be temporarily elevated by strenuous exercise, orthostatic proteinuria, dehydration, urinary tract infections
Glucose: Uncontrolled diabetes mellitus can lead to presence of glucose in urine.
Ketones: Uncontrolled diabetes mellitus can lead to presence of ketones in urine.
Blood: Occult blood can occur in urine in various urological, nephrological and bleeding disorders.
Leukocytes: Most common cause is bacterial urinary tract infection.
Nitrite: Many bacteria give positive results when their number is high.
pH: Conditions of the body producing acidosis/ alkalosis or ingestion of certain type of food can affect the pH of urine.
Specific gravity: Increased S.G. is seen in conditions like dehydration, glycosuria and proteinuria. Decreased S.G. seen in excessive fluid intake,
renal failure and diabetes insipidus.
Bilirubin: In certain liver diseases such as biliary obstruction or hepatitis, bilirubin gets excreted in urine.
Urobilinogen: Positive results are seen in liver diseases like hepatitis, cirrhosis and haemolytic anaemia.
*** End Of Report ***
Barcode No : PPS0058951
Sample Type : URINE.
Page 3 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:43
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- HEMATOLOGY
Complete Blood Count (CBC)
Test Name Result Your Value Reference Range
Hemoglobin (Hb), g/dL 14.6 Normal 12-15
[Method: Spectrophotometry ]
Red Blood Cell (RBC) Count, 4.94 High 3.8-4.8
Million/[Link]
[Method: Impedence]
Packed Cell Volume (PCV) / Hematocrit, 43.9 Normal 36-46
%
[Method: Calculated]
Mean Corpuscular Volume (MCV), fL 88.9 Normal 83-101
[Method: Calculated]
Mean Corpuscular Hemoglobin (MCH), 29.5 Normal 27-32
pg
[Method: Calculated]
Mean Corpuscular Hb Concentration 33.2 Normal 31.5-34.5
(MCHC), g/dL
[Method: Calculated]
Red Cell Distribution Width (RDW), % 13.2 Normal 11.6-14
[Method: Calculated]
Total Leucocyte Count (TLC), cells/µL 9840 Normal 4000 - 11000
[Method: Impedence]
Differential Leucocyte Count (DLC)
Neutrophils, % 54.9 Normal 40 - 75
Lymphocytes, % 36.7 Normal 20 - 40
Monocytes, % 5.2 Normal 0-6
Eosinophils, % 3.0 Normal 00 - 06
Basophils, % 0.2 Normal 1-2
[Method: Impedence & FCM]
Absolute Leucocyte Count
Barcode No : PPS0058952
Sample Type : WHOLE BLOOD EDTA
Page 4 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:43
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- HEMATOLOGY
Neutrophils, Cells/[Link] 5402.16 Normal 2000-7000
[Method: Calculated]
Lymphocytes, Cells/[Link] 3611.28 High 1000-3000
[Method: Calculated]
Monocytes, Cells/[Link] 511.68 Normal 200-1000
[Method: Calculated]
Eosinophils, Cells/[Link] 295.2 Normal 10-600
Basophils, Cells/[Link] 19.68 Normal 0-100
[Method: Calculated]
Platelet Count, 10^3/µl 244 Normal 150-410
[Method: Impedence]
Mean Platelet Volume (MPV), fL 9.4 Normal 7.6-9.6
Interpretation:
CBC provides information about red cells, white cells and platelets. Results are useful in the diagnosis of anemia, infections, leukemia’s,
clotting disorders and many other medical conditions.
*** End Of Report ***
Barcode No : PPS0058952
Sample Type : WHOLE BLOOD EDTA
Page 5 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:41
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- SEROLOGY
Hepatitis B surface Antigen (HBsAg), Rapid method
Test Name Result Reference Range
Hepatitis B surface Antigen (HBsAg), Rapid Non Reactive Non Reactive
method
[Method: Rapid Immunochromatography]
Interpretation:
This is a visual and rapid one step screening immunoassay based on the antigen capture, or “sandwich” principle for the qualitative detection of
Hepatitis B Surface Antigen (HBsAg) in human serum or plasma. The assay is intended to be used as an aid in the recognition and diagnosis of
acute infections and chronic infectious carriers of the Hepatitis B Virus (HBV).
Samples found to be reactive by the above screening test must be rechecked by confirmatory test.
False positive results can be obtained due to the presence of RA antibodies, patients with auto- immune disease, liver problems, renal disorders
and antenatal samples.
A non-reactive result does not exclude the possibility of exposure to or infection with HBV. Additional follow up testing using available clinical
methods is required if this test is non-reactive with persisting clinical symptoms.
For a definitive diagnosis, the patient’s clinical history, symptomatology as well as results of supplemental and confirmatory assays should be
considered.
*** End Of Report ***
Barcode No : PPS0058949
Sample Type : SERUM
Page 6 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:41
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- SEROLOGY
Hepatitis C Antibodies (HCV), CLIA/ELISA
Test Name Result Reference Range
Hepatitis C Antibodies (HCV) Non Reactive Non reactive
Interpretation:
Result (Cut off index) Result Interpretation
< 0.9 Non-reactive
≥ 0.9 to < 1.0 Borderline
≥ 1.0 Reactive
HCV antibodies are usually not detectable during the first 2 months following infection, and they are usually
detectable by the late convalescent stage (>6 months after onset) of infection.
The detection of anti‑HCV antibodies indicates a present or past infection with hepatitis C virus, but does not
differentiate between acute, chronic or resolved infection. It cannot be used to monitor the efficacy of treatment.
Reactive test should be confirmed by more HCV-specific tests, such as direct detection of HCV RNA by RT-PCR
assay.
For diagnostic purposes, the results should always be assessed in conjunction with the patient’s medical history,
clinical examination and other findings.
*** End Of Report ***
Barcode No : PPS0058949
Sample Type : SERUM
Page 7 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:41
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- SEROLOGY
HIV 1 & 2 Antibodies, Rapid
Test Name Result Reference Range
HIV 1 & 2 Antibodies, Rapid Non Reactive Non Reactive
Interpretation:
This is a visual and rapid screening immunoassay for the differential detection of Human Immunodeficiency Virus (HIV-1 & HIV-2) antibodies
(IgM, IgG & IgA) in human serum or plasma using HIV-1 & HIV-2 antigens immobilized on a membrane and detected via a Lateral flow
Immunochromatography technique.
HIV-1 and HIV-2 viruses share many morphological and biological characteristics. It is likely that due to this, their antibodies have a cross
reactivity of 30-70%. Reactivity for HIV-1 and HIV-2 antibodies on the test device does not necessarily imply co-infection from HIV-1 & HIV-2.
Antibody Testing may not be reliable in the following situation:
1. Window Period (Not Detectable during this phase).
2. <18 months of age (Babies of HIV positive mothers may have passively acquired maternal antibodies and hence it is difficult to
differentiate them from those produced by the infant.
False reactivity could be seen in cases of naturally occurring antibodies, passive immunization, certain infections, renal disorders,
hypergammaglobulinemia, neoplasms, rheumatoid arthritis, tetanus vaccination, autoimmune diseases, blood transfusion, hemophilia and
lipemic samples.
Samples found to be reactive by the above screening test must be confirmed by standard supplemental assays, like Western Blot.
A non-reactive result does not exclude the possibility of exposure to or infection with HIV.
For a definitive diagnosis, the patient’s clinical history, symptomatology as well as results of supplemental and confirmatory assays should be
considered.
Barcode No : PPS0058949
Sample Type : SERUM
Page 8 of 9
Patient Name: [Link] VIDHATE Collected : 09 Jul 26 18:32
Gender: Female Received: 09 Jul 26 18:41
Age: 28 Y 7 M 26 D Reported: 09 Jul 26 22:40
MPID: 1000000102832032 Report Status: Final Report
Referred by: . Visit ID/Ref No: OPD/PPS/27P1157
Department- SEROLOGY
*** End Of Report ***
Barcode No : PPS0058949
Sample Type : SERUM
Page 9 of 9