PUP1051481

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Name : MRS.MANISHA TID/SID : PUP1051481/ 23334940

Age / Gender : 29 Years / Female Registered on : 24-Mar-2022 / 10:25 AM
Ref.By : MED LABS DIAGNOSTICS Collected on : 24-Mar-2022 / 11:15 AM
BIL1902057 Reported on : 24-Mar-2022 / 13:07 PM

Req.No : Med Labs Diagnostics
Reference
BIL1902057 TEST REPORT
DEPARTMENT OF CLINICAL PATHOLOGY

Complete Urine Examination (CUE), Urine
Investigation Result Biological Reference Intervals
Physical Examination
Colour Pale Yellow Straw to Yellow
Method:Physical
Appearance Clear Clear
Method:Physical
Chemical Examination
Reaction and pH Acidic (6.5) 4.6-8.0
Method:Methyl Red & Bromothymol Blue
Specific Gravity 1.015 1.003-1.035
Method:Bromothymol Blue
Protein Negative Negative
Method:Tetrabromophenol blue
Glucose Negative Negative
Method:Glucose oxidase/Peroxidase
Blood Negative Negative
Method:Peroxidase
Ketones Negative Negative
Method:Sodium Nitroprusside
Bilirubin Negative Negative
Method:Dichloroanilinediazonium
Leucocytes Negative Negative
Method:3 hydroxy5 phenylpyrrole + diazonium
Nitrites Negative Negative
Method:Diazonium + 1,2,3,4 tetrahydrobenzo (h) quinolin 3-
ol
Urobilinogen Negative 0.2-1.0 mg/dl
Method:Dimethyl aminobenzaldehyde
Microscopic Examination
Pus Cells (Leukocytes) 1-2 2 - 3 /hpf
Epithelial Cells 1-2 2 - 5 /hpf
RBC (Erythrocytes) Absent Absent
/hpf
Casts Absent Occasional hyaline casts may be seen
Crystals Absent Phosphate, oxalate, or urate crystals may
be seen
Others Nil Nil
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Reference
Method: Semi Quantitative test ,For CUE
Reference: Godkar Clinical Diagnosis and Management by Laboratory Methods, First South Asia edition. Product kit
literature.
Interpretation:
The complete urinalysis provides a number of measurements which look for abnormalities in the urine. Abnormal results
from this test can be indicative of a number of conditions including kidney disease, urinary tract infecation or elevated
levels of substances which the body is trying to remove through the urine . A urinalysis test can help identify potential
health problems even when a person is asymptomatic. All the abnormal results are to be correlated clinically.
* Sample processed at Tenet National Reference Laboratory, Hyderabad

51 Kineta Towers, Banjara Hills
--- End Of Report ---
Dr.K Sucharita
Consultant Pathologist
Tenet Diagnostics, Hyderabad
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Reference
DEPARTMENT OF HEMATOLOGY
Blood Grouping ABO And Rh Typing, EDTA Whole Blood
Parameter Results
Blood Grouping (ABO) AB
Rh Typing (D) POSITIVE
Method: Hemagglutination Tube Method by Forward & Reverse Grouping
Reference: Tulip kit literature
Interpretation: The ABO grouping and Rh typing test determines blood type grouping (A,B, AB, O ) and the Rh factor
(positive or negative). A person's blood type is based on the presence or absence of certain antigens on the surface of
their red blood cells and certain antibodies in the plasma. ABO antigens are poorly expresses at birth, increase
gradually in strength and become fully expressed around 1 year of age.
In case of Rh(D) - Du(weak positive) or Weak D positive, the individual must be considered as Rh positive as donor and
Rh negative as recipient.
Note: Records of previous blood grouping/Rh typing not available. Please verify before transfusion.

Dr.Sreedevi D
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Reference
Complete Blood Picture (CBP), EDTA Whole Blood
Investigation Observed Value Biological Reference Interval
Hemoglobin 13.6 12.0-15.0 g/dL gm/dL
Method:Spectrophotometry
PCV/HCT 40.7 36.0-46.0 vol%
Method:Calculated
Total RBC Count 4.61 3.80-4.80 mill /cu.mm
Method:Electrical Impedance
MCV 88.3 83.0-101.0 fL
Method:Calculated
MCH 29.5 27.0-32.0 pg
Method:Calculated
MCHC 33.5 31.5-34.5 g/dL
Method:Calculated
RDW (CV) 13.9 11.6-14.0 %
Method:Calculated
MPV 11.2 7.0-10.0 fL
Method:Calculated
Total WBC Count 9550 4000-10000 cells/cumm
Platelet Count 2.87 1.50-4.10 lakhs/cumm
Differential Count
Neutrophils 73.3 40.0-80.0 %
Lymphocytes 18.2 20.0-40.0 %
Eosinophils 2.8 1.0-6.0 %
Monocytes 5.4 2.0-10.0 %
Basophils 0.3 0.0-2.0 %
Method:Flow Cytometer - Microscopy
Absolute Neutrophil Count 7000.15 2000-7000 cells/cumm
Absolute Lymphocyte Count 1738.1 1000-3000 cells/cumm
Absolute Eosinophil Count 267.4 20-500 cells/cumm
Absolute Monocyte Count 515.7 200-1000 cells/cumm
Absolute Basophil Count 28.65 20-100 cells/cumm
Method:Calculated
Neutrophil - Lymphocyte Ratio(NLR) 4.03 0.78-3.53
Method:Calculated
Peripheral Blood Smear Examination
RBC Normocytic Normochromic
WBC Normal in Morphology & Distribution
Platelets Adequate
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Reference
Method: Automated Hematology Analyzer, Microscopy
Reference: Dacie and Lewis Practical Hematology,12th Edition
Interpretation: A Complete Blood Picture (CBP) is a screening test which can aid in the diagnosis of a variety of
conditions and diseases such as anemia, leukemia, bleeding disorders and infections. This test is also useful in
monitoring a person's reaction to treatment when a condition which affects blood cells has been diagnosed. All the
abnormal results are to be correlated clinically.
Note: These results are generated by a fully automated hematology analyzer and the differential count is computed
from a total of several thousands of cells. Therefore the differential count appears in decimalised numbers and may not
add upto exactly 100. It may fall between 99 and 101.

Dr.Sreedevi D
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DEPARTMENT OF IMMUNOLOGY
Hepatitis B Surface Antigen (HbsAg), Serum
Investigation Observed value Biological Reference Interval
Hepatitis B Surface Antigen(HbsAg) 0.17 (Negative) <1.0: Negative S/Co
Method:CMIA
>=1.0: Positive S/Co
Interpretation:
This test is used to screen for infection with the Hepatitis B (Hep B) virus. The Surface Antigen test looks for a protein
which is present on the surface of the virus. This protein will be present in the blood with an acute or chronic Hep B
infection.
A Negative test result does not exclude possibility of exposure to or infection with Hepatitis B Virus. Levels of HbsAG
may be undetectable both in early infection and in late after infection.
Hepatitis C Antibody (Anti-HCV), Serum
Investigation Observed value Biological Reference Interval
Hepatitis C Antibody (Anti-HCV) 0.09 (Non-Reactive) Non-Reactive: <1.0 S/Co
Method:CMIA
Reactive: >=1.0 S/Co
Interpretation:
Hepatitis C Antibody test is a screening test to detect antibodies which develop in response to Hepatitis C (HCV)
infections. These antibodies are usually detectable at 4-12 weeks or greater after exposure.
A negative result does not exclude the possibility of infection with HCV. These antibodies may be undetectable in early
stages of infection,This is a screening assay, all positive results should be confirmed by other supplementary methods
like HCV RNA detection assay.
HIV 1 & 2 Antibodies, Serum
Investigation Observed Values Biological Reference Value
HIV Ag/Ab 0.10 (Non-Reactive) < 1.0 : Non-Reactive S/Co
Method:CMIA
>= 1.0 : Reactive S/Co
Interpretation: Non-reactive : Specimen Negative for HIV.
Reactive : Specimen Positive for HIV(HIV-1,HIV-2)
A negative result does not exclude the possibility of infection with HIV. Levels of HIV Antibodies may be undetectable in
the window period.
This is a screening assay, all positive results should be confirmed by other supplementary methods like Western Blot
Assay / HIV PCR.
VDRL (RPR), Serum

Investigation Result Biological Reference Range
VDRL (RPR) Non-Reactive Non-Reactive
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Reference
Method: Slide Flocculation

Note : Significant
Diagnostic titre 1:8, Biological false positives possible. Repeat testing should be
done with a specific test like TPHA for low titres such as 1:1, 1:2 and 1:4.
Reference: Kit insert Carbogen Tulip diagnostics (P) Ltd.
Interpretation:
The Rapid Plasma Reagin(RPR)/Carbogen Antigen test is a macroscopic non Treponemal flocculation test for the
detection and quantitation of antilipoidal antibodies.Non-treponemal tests are known to suffer from biological false
positives in many conditions such as pregnancy , malaria and many other infectious diseases. In abscence of
supporting clinical, historical or epidimiological evidence , reactive results must be confirmed with more specific
treponemal tests.

Dr.Safaa Muneer Ahmed

Consultant Microbiologist
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Reference
DEPARTMENT OF CLINICAL BIOCHEMISTRY I

25 - Hydroxy Vitamin D, Serum
25 - Hydroxy Vitamin D 8.59 Deficiency: < 20 ng/mL
Method:CLIA Insufficiency: 20 - 30 ng/mL
Sufficiency: 30 - 100 ng/mL
Toxicity: > 100 ng/mL
Note Kindly correlate clinically
Interpretation: This test is used to measure the level of Vitamin D in the blood. Vitamin D is necessary for the proper
growth and health of teeth and bones. It also helps in the healthy development of the immune system as well as various
tissues throughout the body. Vitamin D typically comes from 2 sources. D3 (cholecalciferol) is produced by the body
when the skin is exposed to sunlight. D2 (ergocalciferol) is found in certain foods as well as vitamins and supplements.
This test provides a combined measurement for D2 and D3.Symptoms of vitamin D deficiency can include tiredness,
weakness, aches and pains and frequent infections. Vitamin D levels measurement diagnoses its deficiency as well as
its toxicity.

Dr Afreen Anwar
Consultant Biochemist
Tenet Diagnostics,Hyderabad
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Name : MRS.MANISHA TID/SID : PUP1051481/ 23334941R


Reference
DEPARTMENT OF CLINICAL BIOCHEMISTRY I

Glucose Random (RBS), Sodium Fluoride Plasma
Glucose Random 91 70-140 mg/dl
Method:Hexokinase
Interpretation: Detect high blood glucose (hyperglycemia) and low blood glucose (hypoglycemia).To Screen for
diabetes. To diagnose diabetes, prediabetes and gestational diabetes and to monitor glucose levels in people
diagnosed with diabetes.
Reference: American Diabetes Association. Standards of Medical Care in Diabetes-2020.

Dr Afreen Anwar
Consultant Biochemist
Tenet Diagnostics,Hyderabad
Page 9 of 9

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TO VERIFY THE REPORT ONLINE

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334940

BIL1902057 Reported on : 24-Mar-2022 / 13:07 PM

DEPARTMENT OF CLINICAL PATHOLOGY

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334940

BIL1902057 Reported on : 24-Mar-2022 / 13:07 PM

Method: Semi Quantitative test ,For CUE

* Sample processed at Tenet National Reference Laboratory, Hyderabad

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334939

BIL1902057 Reported on : 24-Mar-2022 / 13:01 PM

Method: Hemagglutination Tube Method by Forward & Reverse Grouping

Reference: Tulip kit literature

* Sample processed at Tenet National Reference Laboratory, Hyderabad

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334939

BIL1902057 Reported on : 24-Mar-2022 / 13:01 PM

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334939

BIL1902057 Reported on : 24-Mar-2022 / 13:01 PM

Method: Automated Hematology Analyzer, Microscopy

Reference: Dacie and Lewis Practical Hematology,12th Edition

* Sample processed at Tenet National Reference Laboratory, Hyderabad

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334938

BIL1902057 Reported on : 24-Mar-2022 / 16:31 PM

Interpretation: Non-reactive : Specimen Negative for HIV.

Reactive : Specimen Positive for HIV(HIV-1,HIV-2)

VDRL (RPR), Serum

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334938

BIL1902057 Reported on : 24-Mar-2022 / 16:31 PM

Method: Slide Flocculation

* Sample processed at Tenet National Reference Laboratory, Hyderabad

Dr.Safaa Muneer Ahmed

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334938

BIL1902057 Reported on : 24-Mar-2022 / 13:31 PM

DEPARTMENT OF CLINICAL BIOCHEMISTRY I

* Sample processed at Tenet National Reference Laboratory, Hyderabad

Name : MRS.MANISHA TID/SID : PUP1051481/ 23334941R

BIL1902057 Reported on : 24-Mar-2022 / 12:28 PM

DEPARTMENT OF CLINICAL BIOCHEMISTRY I

Reference: American Diabetes Association. Standards of Medical Care in Diabetes-2020.

* Sample processed at Tenet National Reference Laboratory, Hyderabad

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