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Reference No.

: - 2412133085 Age/Gender : 35 Yrs/Female


Pt's Name : Mrs. RICHA GUPTA
DAK-NAM
Referred By : NA
Sample Collection Date/Time : 29-Dec-2024 Date :29-Dec-2024
Sample Receiving Date/Time : 29-Dec-2024 02:00AM Approved Date :29-Dec-2024 05:46AM
Sample From : NAMAN PATHOLOGY LAB Report Print Time :29-Dec-2024 09:47PM

BASIC PROFILE 1
BIOCHEMISTRY
Test Description Observed Value Biological Reference Interval
LIVER FUNCTION TEST (LFT), Serum
Bilirubin, Total 0.20 Adults : 0.0-1.3 mg/dL
(Colorimetric diazomethod) Child(>1months):0.0-1.3 mg/dL
Bilirubin, Direct 0.10 0 - 0.4 mg/dL
Diazo method
Bilirubin, Indirect 0.10 0.0 - 0.80 mg/dL
Calculated
SGOT (AST), Serum 22.40 14 - 36 U/L
IFCC without pyridoxal phosphate activation
SGPT (ALT), Serum 21.90 < 35 U/L
IFCC with pyridoxal phosphate activation
Alkaline Phosphatase (ALP), Serum 109.0 38 - 126 U/L
IFCC Gen.2 Colorimetric assay
Gamma Glutamyl Transferase (GGT)* 28 5-85 U/L
Protein,Total 6.90 6.4-8.7 g/dL
Colorimetric assay
Albumin,Serum 4.30 Adults:3.5-5.2
Bromo Cresol Green Method Newborn 0-4 days:2.8-4.4
Children 4 days-14 yr:3.8-5.4
14-18 years : 3.2-4.5 g/dL
Globulin 2.60 2.30-3.50 g/dL
Calculated
A/G Ratio 1.65
Equipment Used: VITROS® XT 7600 Integrated System [Dry Chemistry]
Equipment measurement : Colorimetric/Rate,Potentiometric (Direct ISEs),Immuno-rate,Turbidimetric,Enhanced Chemiluminescence
COMMENT :
Please correlate with clinical conditions and drug history.
This report is not valid for medico legal purpose.
If the results of the tests are alarming or unexpected, please contact immediately

*** End Of Report ***

Page 1 of 7
Reference No. : - 2412133085 Age/Gender : 35 Yrs/Female
Pt's Name : Mrs. RICHA GUPTA
DAK-NAM
Referred By : NA
Sample Collection Date/Time : 29-Dec-2024 Date :29-Dec-2024
Sample Receiving Date/Time : 29-Dec-2024 02:00AM Approved Date :29-Dec-2024 05:46AM
Sample From : NAMAN PATHOLOGY LAB Report Print Time :29-Dec-2024 09:47PM

Test Description Observed Value Biological Reference Interval


LIPID PROFILE, Serum
Triglyceride 72.7 0.0 - 200 mg/dL
Enzymatic Colorimetric assay
Total Cholesterol 160.0 Desirable: 200
Enzymatic, Colorimetric Method. Borderline: 201-240
High: >240 mg/dL
HDL Cholesterol 39.7 No risk: > 55
Homogeneous Enzymatic Colorimetric assay Moderate risk:35-55
High risk: < 35 mg/dL
VLDL Cholesterol 14.5 15.0 - 40.0 mg/dL
Calculated
LDL Cholesterol 105.8 Optimal: < 100
Calculated Near optimal: 100-129
Borderline high: 130-159
High: 160-189
Very high: >190 mg/dL
Total / HDL Cholesterol Ratio 4.0 3.0 - 6.0 Ratio
Calculated
LDL / HDL Cholestrol Ratio 2.66 0.00 - 3.55 Ratio
Calculated
Equipment Used: VITROS® XT 7600 Integrated System [Dry Chemistry]
Equipment measurement : Colorimetric/Rate,Potentiometric (Direct ISEs),Immuno-rate,Turbidimetric,Enhanced Chemiluminescence

COMMENT :
Tests results are created by fully/semi automated equipments.
This is only a professional opinion, not the diagnosis.
Please correlate with clinical conditions and drug history.
This report is not valid for medico legal purpose.
If the results of the tests are alarming or unexpected, please contact immediately.

*** End Of Report ***

Page 2 of 7
Reference No. : - 2412133085 Age/Gender : 35 Yrs/Female
Pt's Name : Mrs. RICHA GUPTA
DAK-NAM
Referred By : NA
Sample Collection Date/Time : 29-Dec-2024 Date :29-Dec-2024
Sample Receiving Date/Time : 29-Dec-2024 02:00AM Approved Date :29-Dec-2024 05:46AM
Sample From : NAMAN PATHOLOGY LAB Report Print Time :29-Dec-2024 09:47PM

Test Description Observed Value Biological Reference Interval


Kidney Profile, Serum
Urea 25.10 Adults (< 65 y) : < 50 mg/dL
Kinetic test with urease and GLDH
Creatinine 0.60 0.60 - 1.20 mg/dL
Kinetic Colorimetric Jaffé method
Uric Acid, Serum 4.30 2.5-6.2 mg/dL
Enzymatic colorimetric Uricase Peroxidase
Protein, Total 6.90 Adults : 6.40-8.70 g/dL
Biuret Method
Sodium 142.00 136.0-145.0 mEq/L
Direct Ion-Selective Electrode (DISE)
Potassium 5.00 3.50-5.20 mEq/L
Direct Ion-Selective Electrode (DISE)
Chloride 105.0 96-108 mmol/L
Direct Ion-Selective Electrode (DISE)
Calcium, Serum 9.30 8.6 - 10.0 mg/dL
5-Nitro-5-methyl-BAPTA method
Equipment Used: VITROS® XT 7600 Integrated System [Dry Chemistry]
Equipment measurement : Colorimetric/Rate,Potentiometric (Direct ISEs),Immuno-rate,Turbidimetric,Enhanced Chemiluminescence

COMMENT :
Tests results are created by fully/semi automated equipments.
This is only a professional opinion, not the diagnosis.
Please correlate with clinical conditions and drug history.
This report is not valid for medico legal purpose.
If the results of the tests are alarming or unexpected, please contact immediately.

*** End Of Report ***

Page 3 of 7
Reference No. : - 2412133085 Age/Gender : 35 Yrs/Female
Pt's Name : Mrs. RICHA GUPTA
DAK-NAM
Referred By : NA
Sample Collection Date/Time : 29-Dec-2024 Date :29-Dec-2024
Sample Receiving Date/Time : 29-Dec-2024 01:53AM Approved Date :29-Dec-2024 04:59AM
Sample From : NAMAN PATHOLOGY LAB Report Print Time :29-Dec-2024 09:47PM

HAEMATOLOGY
Test Description Observed Value Biological Reference Interval
Complete Blood Count*[6 part Sysmex XN-550], EDTA whole blood
Haemoglobin (Hb)* 13.6 12.0-16.0 g/dL
RBC Count* 4.80 4.00-5.20 Millions/cumm
Packed Cell Volume* 45.9 36-46 %
MCV* 95.0 80-100 fL
MCH* 28.2 26-34 pg
MCHC* 29.6 31-37 g/dL
RDW-CV* 17.0 11.5-14.5 %
ESR * 15 0-20
Westergren method
TLC (Total Leucocyte Count)* 6190 4000-11000 /cumm
Differential Leucocyte Count
Neutrophil* 74.4 40-80 %
Lymphocyte* 17.6 24-44 %
Eosinophils* 3.4 01-06 %
Monocytes* 4.2 2-8 %
Basophils* 0.4 0-1 %
IG %* 0.800 0.0 - 0.40 %
Absolute Neutrophil Count* 4.61 2.0-7.0 x 10^3 /uL
Absolute Lymphocyte Count* 1.090 1.0-3.0 x 10^3/uL
Absolute Eosinophil Count* 0.210 0.02-0.50 10^3/uL
Absolute Monocyte Count* 0.3 0.2-1.0 x 10^3/uL
Absolute Basophil Count* 0.020 0.02-0.10 x 10^3 cells/uL
IG* 0.000 0.0 -0.30 10^3/uL
Platelet Count* 2.10 1.50-4.50 Lakh/cumm
Mean Platelet Volume* 10.40
Plateletcrit* 0.20
PDW [Platelet Distribution Width]* 11.90
P-LCR [Platelet to Large Cell Ratio]* 28.80 19.7 - 42.4 %
Causes of low Hb include: Causes of high Hb include:

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Reference No. : - 2412133085 Age/Gender : 35 Yrs/Female
Pt's Name : Mrs. RICHA GUPTA
DAK-NAM
Referred By : NA
Sample Collection Date/Time : 29-Dec-2024 Date :29-Dec-2024
Sample Receiving Date/Time : 29-Dec-2024 01:53AM Approved Date :29-Dec-2024 04:59AM
Sample From : NAMAN PATHOLOGY LAB Report Print Time :29-Dec-2024 09:47PM

Iron deficiency anemia, Vitamin deficiency anemia. (B12/Folic


Smoking, COPD (chronic obstructive pulmonary disease)exacerbation,
acid),Anemia of inflammation, Aplastic anemia, Anemias associated with
Dehydration, Emphysema, Heart failure,Polycythemia vera
bone marrow disease, Hemolytic anemia etc
Causes of low WBC include: Causes of high WBC include:
Cancer (caused by chemotherapy treatments),Bone marrow disorders or
damage, Autoimmune disorders (problems with the immune system in Infection, Inflammation, Injury, Emotional stress, Labor,
which the body attacks itself), such as lupus, Infections (including Pregnancy,Smoking, Allergic reactions, Excessive exercise, A bone
tuberculosis and HIV),Immune system conditions, Crohn’s disease, marrow or immune disorder, Certain cancers, such as acute or chronic
Malnutrition, Radiation treatments for cancer, Rheumatoid arthritis, leukemia
Vitamin deficiencies, Liver damage and/or enlarged spleen.
Causes of low Platelets include: Causes of high Platelets include:
Acute bleeding and blood loss, Cancer, Infections, Iron
Leukemia and other cancers, Some types of anemia., Viral infections
deficiency,Removal of your spleen, Inflammatory disorders, such as
such as Dengue, Hepatitis C or HIV, Chemotherapy drugs and radiation
rheumatoid arthritis, sarcoidosis or inflammatory bowel disease, Surgery
therapy, Heavy alcohol consumption, ITP
or other type of trauma, Essential thrombocythemia

Please Correlate with clinical conditions.

Instrument : Fully automated bidirectional hematology analyser (6 part differential Sysmex XN-550)
Method : Hematology analyses according to the Hydrodynamic Focussing [DC method],
Flow Cytometry Method [Using a semiconductor laser], and SLS- hemoglobin method.
Sample : EDTA whole blood in cool condition

*** End Of Report ***

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Reference No. : - 2412133085 Age/Gender : 35 Yrs/Female
Pt's Name : Mrs. RICHA GUPTA
DAK-NAM
Referred By : NA
Sample Collection Date/Time : 29-Dec-2024 Date :29-Dec-2024
Sample Receiving Date/Time : 29-Dec-2024 01:53AM Approved Date :29-Dec-2024 03:11AM
Sample From : NAMAN PATHOLOGY LAB Report Print Time :29-Dec-2024 09:47PM

Test Description Observed Value Biological Reference Interval


HbA1c (Glycated Haemoglobin), EDTA Plasma 6.0 4.5-6.4 %
High Pressure Liquid Chromatograpy
REMARKS
In vitro quantitative determination of HbA1c in whole blood is utilized in long term monitoring of glycemia.The HbA1c level correlates with the mean glucose concentration prevailing in
the course of the patient's recent history (approx - 6-8 weeks) and therefore provides much more reliable information for glycemia monitoring than do determinations of blood glucose or
urinary glucose. It is recommended that the determination of HbA1c be performed at intervals of 4-6 weeks during Diabetes Mellitus therapy. Results of HbA1c should be assessed in
conjunction with the patient's medical history, clinical examinations and other findings.
Mean Plasma Glucose, EDTA Plasma 125.50 mg/dL
Calculated
Mean Plasma Glucose is based on estimated Average Glucose (eAG) value calculated according to National Glycohemoglobin Standardization Program (NGSP) criteria.

Reference Range (HBA1c) :


Good control : 4.5 - 6.4 %
Fair control : 6.5 - 7.4 %
Poor control : Above - 7.5 %

Reference Range (Average Blood Sugar):

Excellent control : 90 - 120 mg/dl


Good control : 121 - 150 mg/dl
Average control : 151 - 180 mg/dl
Action suggested : 181 - 210 mg/dl
Panic value : > 211 mg/dl

[Note: Average blood sugar values is calculated from hba1c value and it indicates average blood sugar level over past three months.]

*** End Of Report ***

Page 6 of 7
Reference No. : - 2412133085 Age/Gender : 35 Yrs/Female
Pt's Name : Mrs. RICHA GUPTA
DAK-NAM
Referred By : NA
Sample Collection Date/Time : 29-Dec-2024 Date :29-Dec-2024
Sample Receiving Date/Time : 29-Dec-2024 02:00AM Approved Date :29-Dec-2024 05:11AM
Sample From : NAMAN PATHOLOGY LAB Report Print Time :29-Dec-2024 09:47PM

IMMUNOASSAY
Test Description Observed Value Biological Reference Interval
T3 T4 TSH,Serum
Triiodothyronine, Total (T3), Serum 131 60-181 ng/dL
Chemiluminescence Immuno Assay
Thyroxine, Total (T4), Serum 8.6 4.5-10.9 ug/dL
Chemiluminescence Immuno Assay
3rd Gen. ( TSH Ultrasensitive ),Serum 2.24 0.35-5.50 ulU/mL
Chemiluminescence Immuno Assay
COMMENT :
The levels of thyroid hormone (T3 & T4) Are Low In case of Primary, secondary and tertiary hypothyroidism and sometimes in non-thyroidal illness also.
Increased levels are found in grave’s disease, hyperthyroidism and thyroid hormone resistance. T3 levels are also raised in T3 thyrotoxicosis. TSH levels are raised
in primary hypothyroidism and are low in hyperthyroidism and secondary hypothyroidism.

In Pregnancy:

LEVEL TOTAL T3 TOTAL T4 TSH


Ist Trimester 81-190 6.6-12.4 0.1-2.5
IInd Trimester 100-260 6.6-15.5 0.2-3.0
IIIrd Trimester 100-260 6.6-15.5 0.3-3.0

*** End Of Report ***

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