PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022825 / 12708591 Report Date : 30/Apr/2025 03:53PM
Sample Type : EDTA Report Status : Final Report

HAEMATOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

Complete Blood Count

Hemoglobin 15.5 g/dL 13.0-17.0 Spectrophotometry
(Cyanide-free)
RBC 5.58 mili/cu.mm 4.5 - 5.5 Impedence
HCT 46.1 % 40 - 50 Calculated
MCV 82.6 fL 83 - 101 Calculated
MCH 27.7 pg 27 - 32 Calculated
MCHC 33.5 g/dL 31.5 - 34.5 Calculated
RDW-CV 12.8 % 11.5-14 Calculated
Total Leucocyte Count 6.43 10^3/µL 4 - 10 Impedance
Differential Leucocyte Count
Neutrophils 48.8 % 40-80 DHSS/Microscopy
Lymphocytes 38.2 % 20-40 DHSS/Microscopy
Monocytes 10.4 % 2-10 DHSS/Microscopy
Eosinophils 2.5 % 1-6 DHSS/Microscopy
Basophils 0.1 % 0-2 Impedance/Microscopy
Absolute Leucocyte Count
Absolute Neutrophil Count 3.14 10^3/µL 2-7 Calculated
Absolute Lymphocyte Count 2.46 10^3/µL 1-3 Calculated
Absolute Monocyte Count 0.67 10^3/µL 0.2 - 1 Calculated
Absolute Eosinophil Count 0.16 10^3/µL 0.02 - 0.5 Calculated
Absolute Basophil Count 0.01 10^3/µL 0.02-0.1 Calculated
Platelet Count 180 10^3/µL 150-410 Impedance/Microscopy
MPV 11.7 fL 6.5 - 12 Calculated
PDW 22.8 fL 9-17 Calculated

Comment:
As per the recommendation of International council for Standardization in Hematology, the differential leucocyte counts are
additionally being reported as absolute numbers of each cell in per unit volume of blood.
DHSS : Double Hydrodynamic Sequential System Flowcytometry
Calculated parameters are either derived from Impedence measure, RBC pulse measurement, RBC/platelet histograms or
formula derived.

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 1 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022825 / 12708591 Report Date : 30/Apr/2025 03:53PM
Sample Type : EDTA Report Status : Final Report

HAEMATOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
Erythrocyte Sedimentation Rate
Erythrocyte Sedimentation Rate 1 mm/hr 0-10 Modified Westergren at
18C

Comment:

ESR provides an index of progress of the disease and is widely used as an indicator of inflammation, infection, trauma, or
malignant diseases. Changes are more significant than a single abnormal test
It is specifically indicated to monitor the course or response to the treatment of diseases like rheumatoid arthritis,
tuberculosis bacterial endocarditis ,acute rheumatic fever ,Hodgkins disease,temporal arthritis , and systemic lupus
erythematosis; and to diagnose and monitor giant cell arteritis and polymyalgia rheumatica.
An elevated ESR may also be associated with many other conditions, including autoimmune disease, anemia,
infection,malignancy,pregnancy, multiple myeloma, menstruation, and hypothyroidism.
Although a normal ESR cannot be taken to exclude the presence of organic disease, its rate is dependent on various
physiologic and pathologic factors.
The most important component influencing ESR is the composition of plasma. High level of C-Reactive Protein, fibrinogen,
haptoglobin, alpha-1antitrypsin, ceruloplasmin and immunoglobulins causes the elevation of Erythrocyte Sedimentation
Rate.
Drugs that may cause increase ESR levels include: dextran, methyldopa, oral contraceptives, penicillamine, procainamide,
theophylline, and Vitamin A. Drugs that may cause decrease levels include: aspirin, cortisone, and quinine

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 2 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022825 / 12708591 Report Date : 30/Apr/2025 02:42PM
Sample Type : WHOLE BLOOD-EDTA Report Status : Final Report

HAEMATOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

HbA1c (Glycosylated Hemoglobin)

Glycosylated Hemoglobin (HbA1c) 5.0 % 4-5.6 HPLC (NGSP certified)
Estimated average glucose (eAG) 96.80 mg/dL Calculated

Comment:
Interpretation: HbA1c%

≤5.6 Normal
5.7-6.4 At Risk For Diabetes
≥6.5 Diabetes

Adapted from American Diabetes Association.

Comments:
A 3 to 6 monthly monitoring is recommended in diabetics. People with diabetes should get the test done more often if their blood
sugar stays too high or if their healthcare provider makes any change in the treatment plan. HbA1c concentration represent the
integrated values for blood glucose over the preceding 8-12 weeks and is not affected by daily glucose fluctuation, exercise &
recent food intake.
Please note, Glycemic goal should be individualized based on duration of diabetes, age/life expectancy, comorbid conditions,
known CVD or advanced microvascular complications, hypoglycemia unawareness, and individual patient considerations.

Factors that interfere with HbA1c Measurement: Hemoglobin variants, elevated fetal hemoglobin (HbF) and chemically modified
derivatives of hemoglobin (e.g. carbamylated Hb in patients with renal failure) can affect the accuracy of HbA1c measurements.

Factors that affect interpretation of HbA1c Measurement: Any condition that shortens erythrocyte survival or decrease mean
erythrocyte age (e. g., recovery from acute blood loss, hemolytic anemia, HbSS, HbCC, and HbSC) will falsely lower HbA1c test
results regardless of the assay method used. Iron deficiency anemia is associated with higher HbA1c.

Note: Presence of Hemoglobin variants and/or conditions that affect red cell turnover must be considered, particularly when the
HbA1c result does not correlate with the patient's blood glucose levels.

• HPLC - High performance liquid chromatography

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 3 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022824 / 12708591 Report Date : 30/Apr/2025 02:05PM
Sample Type : Fluoride Plasma F Report Status : Final Report

BIOCHEMISTRY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

FBS (Fasting Blood Sugar)

Glucose - Fasting 85 mg/dL 70-99 Hexokinase/G-6-PDH

Fasting Plasma Glucose (mg/dL) 2 hr plasma Glucose (mg/dL) Diagnosis

99 or below 139 or below Normal
100 to 125 140 to 199 Pre-Diabetes (IGT)
126 or above 200 or above Diabetes

Reference : American Diabetes Association

Comment:
Impaired glucose tolerance (IGT) fasting, means a person has an increased risk of developing type 2 diabetes but does not
have it yet. A level of 126 mg/dL or above, confirmed by repeating the test on another day, means a person has diabetes.
IGT (2 hrs Post meal ), means a person has an increased risk of developing type 2 diabetes but does not have it yet. A 2-hour
glucose level of 200 mg/dL or above, confirmed by repeating the test on another day, means a person has diabetes

Plasma Glucose Goals For people with Diabetes

Before meal 70-130 mg/dL
2 Hours after meal Less than 180 mg/dL
Less than 7%
HbA1c

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 4 of 17
PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 06:22PM
Sample Type : Serum Report Status : Final Report

BIOCHEMISTRY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

Lipid Profile
Cholesterol - Total 181 mg/dL Low (desirable): < 200 Enzymatic
mg/dL
Moderate (borderline)
200–239 mg/dL
High: >/= 240 mg/dL
Triglycerides 143 mg/dL Normal: <150, Glycerol Phosphate
Borderline: 150 - 199, Oxidase
High:200-499,
Very High>=500
Cholesterol - HDL 36 mg/dL Undesirable/high risk Accelerator Selective
<40mg/dL Detergent
Desirable/low
risk>=60mg/dl
Cholesterol - LDL 116 mg/dl Desirable: <100 Calculated
Above desirable: 100 -
129
Borderline high : 130 -
159
High : 160 - 189
Very high : >=190
Cholesterol- VLDL 29 mg/dl <30 Calculated
Cholesterol : HDL Cholesterol 5.0 Ratio Desirable : 3.5-4.5 Calculated
High Risk : >5
LDL : HDL Cholesterol 3.18 Ratio Desirable : 2.5-3.0 Calculated
High risk : >3.5
Non HDL Cholesterol 144 mg/dL Desirable:< 130, Calculated
Above Desirable:130 -
159,
Borderline High:160 -
189,
High:190 - 219,
Very High: >= 220

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 5 of 17
PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 06:22PM
Sample Type : Serum Report Status : Final Report

BIOCHEMISTRY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

Comment:
•Lipid profile measurements in the same patient can show physiological & analytical variations. It is recommended that 3 serial
samples 1 week apart may be tested.
•Indians are at a high risk of developing atherosclerotic cardiovascular disease (ASCVD); at a much earlier age and more severe
with high mortality. Dyslipidemia (abnormal lipid profile) is the major risk factor and found in almost 80% Indians.
•Total cholesterol is the total amount of cholesterol in blood comprising of HDL, LDL-C, and VLDL.
•LDL Cholesterol (LDL-C) or “bad”cholesterol contributes most significantly to atherosclerosis leading to heart disease or
stroke and is the primary target for reducing risk for cardiovascular disease.
•High-density lipoprotein (HDL) or “good” cholesterol can lower risk of heart disease and stroke.
•Triglyceride (TG) level also plays a major role in CVD. Indians are more prone to Atherogenic dyslipidemia, a condition
associated with high TG, low HDL-C and high LDL-C; this is associated with diabetes, metabolic syndrome and insulin resistance.
Hence high triglyceride levels also need to be treated.
•Non-HDL-Cholesterol (Non-HDLC) measures all plaque forming lipoproteins (e.g. remnants, LDL-C, VLDL, Lp(a), Apo-B).
Monitoring of Non-HDLC is important in patients with high TG (e.g. diabetics, obese persons) and those already on statin
therapy.
•Lipid Association of India (LAI-2020) recommends:-

Screening of all Indians above the age of 20 years for CVD risk factors, esp. lipid profile.
Identification of Risk factors: Age (male ≥45 years, female ≥55 years); Family h/o heart disease at younger age (<55 yrs
in males, <65 yrs in female), Smoking/tobacco use, High blood pressure, Low HDL (males <40 mg/dl and females
<50mg/dl).
Fasting lipid profile is not mandatory for screening. Both fasting and non-fasting lipid profiles are equally important for
managing Indian patients.
Non-HDLC should be calculated in every subject. LAI recommends LDL-C as the primary target and Non-HDLC as the co-
primary target for initiating drug therapy.
Lifestyle modifications are of first and foremost importance for management and prevention of dyslipidemia. Among low
risk groups, treatment is started only after 3 months of lifestyle changes.
Testing for Apolipoprotein B, hsCRP, Lp(a ) should be considered for patients in moderate risk group.
Newer treatment goals based on Risk Groups and values of LDL-C and Non-HDLC

New treatment goals by Lipid Association of India (2020)

CONSIDER THERAPY (cut-off level) TREATMENT GOALS
Risk groups LDL-C (mg/dL) Non-HDLC (mg/dL) LDL-C (mg/dL) Non-HDLC (mg/dL)
<50 <80
Extreme Risk Gp Cat. A ≥50 ≥80
(Optional ≤30) (Optional ≤60)
Extreme Risk Gp Cat. B >30 >60 ≤30 ≤60
Very High Risk ≥50 ≥80 <50 <80
High Risk ≥70 ≥100 <70 <100
Moderate Risk ≥100 ≥130 <100 <130
Low risk ≥130* ≥160* <100 <130
*After an adequate non-pharmacological intervention for at least 3 months

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 6 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 06:22PM
Sample Type : Serum Report Status : Final Report

BIOCHEMISTRY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
•As per NCEP Expert Panel (2011) guidelines, universal screening for dyslipidemia is recommended for children between 9
- 11 yrs (repeat at 17-21 yrs). Screening is not recommended before the age of 2yrs. Above the age of 2 yrs, selective screening
is done in children with family history of premature CVD or risk factors like obesity, diabetes, and hypertension.

Note: Reference Interval as per National Cholesterol Education Program (NCEP) Report.
*Please note the change in BRI

LIVER FUNCTION TEST

Liver Function Test
Bilirubin-Total 0.50 mg/dL 0.3-1.2 Diazonium Salt
Bilirubin-Direct 0.18 mg/dL 0-0.5 Diazo
Bilirubin-Indirect 0.32 mg/dL 0.2 - 0.8 Calculated
Protein, Total 6.90 g/dL 6.4-8.3 Biuret
Albumin 4.73 g/dL 3.5-5.0 Bromocresol Green
Globulin 2.2 g/dL 2.1 - 3.9 Calculated
A/G Ratio 2.18 Ratio 0.8 - 2.1 Calculated
Aspartate Transaminase (SGOT) 33 U/L 11-34 NADH w/o P-5’-P
SGPT (Alanine Transaminase) 45 U/L 0-45 NADH w/o P-5’-P
SGOT/SGPT 0.73 Ratio Calculated
Alkaline Phosphatase 73 U/L 40-150 Para-Nitrophenyl
Phosphate
Gamma Glutamyltransferase (GGT) 26 U/L 12-55 L-gamma-glutamyl-3-
Carboxy-4-Nitroanilide

Comment:

Raised ALT and AST indicate hepatocellular damage (e.g. viral or drugs etc). ALT is more liver-specific while AST is also
found in heart, skeletal muscle, and kidney. Mild elevation (less than twice normal) often resolves on its own. Fatty liver
disease (especially with metabolic syndrome) is a common cause in asymptomatic cases. Certain drugs (paracetamol,
statins), herbal supplements, energy drinks, and antibiotics may also affect liver function.
SGOT/SGPT Ratio: Typically <1 in healthy individuals (vary between 0.7-1.4; higher in women than men). High SGPT (ratio
<1) seen in acute or chronic hepatitis, autoimmune disorders, medications, toxins while ratio >1 indicates alcoholic
hepatitis, cirrhosis, metastasis or non-hepatic issues (hemolytic diseases, CVS disorders).
Elevated Alkaline Phosphatase and GGT: Suggest cholestatic diseases (e.g. bile duct obstruction, primary biliary
cirrhosis etc.) and can also be due to bone disease, pregnancy, chronic renal failure, malignancy, and congestive heart

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 7 of 17
PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 06:22PM
Sample Type : Serum Report Status : Final Report

BIOCHEMISTRY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
failure.
High Bilirubin: Indicates jaundice due to increased RBC breakdown, liver damage (e.g., infections, toxins), or cholestasis
(e.g., gallstones, tumors).
High Protein Levels: Seen in dehydration (e.g., severe vomiting, diarrhea) or increased production (e.g., inflammation,
hematopoietic neoplasms). Low protein and albumin: Result from impaired synthesis (liver disease), decreased intake,
tissue damage, malabsorption, or increased renal excretion.

*Please note the change in BRI.

*Please note test values may vary depending on the assay method used.

Kidney Function Test.

Blood Urea Nitrogen 6 mg/dL 8.9-20.6 Urease
Urea 12.84 mg/dL 19.0 - 44.0 Calculated
Creatinine 0.96 mg/dL 0.6-1.2 Kinetic Alkaline Picrate
Uric Acid 7.1 mg/dL 3.7-7.7 Uricase
Sodium 143 mmol/L 136-145 INDIRECT ISE
Potassium 3.57 mmol/L 3.5-5.1 INDIRECT ISE
Chloride 107.0 mmol/L 98-107 INDIRECT ISE
BUN/Creatinine Ratio 6.2 Ratio 12:1 - 20:1 Calculated

Comment:
BUN is directly related to protein intake and nitrogen metabolism and inversely related to the rate of excretion of urea.Blood
urea nitrogen (BUN) levels reflect the balance between the production and excretion of urea. Increased levels are seen in renal
failure (acute or chronic), urinary tract obstruction, dehydration, shock, burns, CHF, GI bleeding, nephrotoxic drugs. Decreased
levels are seen in hepatic failure, nephrotic syndrome, cachexia (low-protein and high-carbohydrate diets).
Urea is a non-proteinous nitrogen compound formed in the liver from ammonia as an end product of protein metabolism. Urea
diffuses freely into extracellular and intracellular fluid and is ultimately excreted by the kidneys. Increased levels are found in
acute renal failure, chronic glomerulonephritis, congestive heart failure, decreased renal perfusion, diabetes, excessive protein
ingestion, gastrointestinal (GI) bleeding, hyperalimentation, hypovolemia, ketoacidosis, muscle wasting from starvation,
neoplasms, pyelonephritis, shock, urinary tract obstruction, nephrotoxic drugs. Decreased levels are seen in inadequate dietary
protein, low-protein/high-carbohydrate diet, malabsorption syndromes, pregnancy, severe liver disease, certain drugs.
Creatinine is catabolic product of creatinine phosphate, which is excreted by filtration through the glomerulus and by tubular
secretion. Creatinine clearance is an acceptable clinical measure of glomerular filtration rate (GFR). Increased levels are seen in
acute/chronic renal failure, urinary tract obstruction, hypothyroidism, nephrotoxic drugs, shock, dehydration, congestive heart
failure, diabetes. Decreased levels are found in muscular dystrophy.
BUN/Creatinine ratio (normally 12:1–20:1) is decreased in acute tubular necrosis, advanced liver disease, low protein intake,
and following hemodialysis. BUN/Creatinine ratio is increased in dehydration, GI bleeding, and increased catabolism.
Uric acid levels show diurnal variation. The level is usually higher in the morning and lower in the evening. Increased levels are
seen in starvation, strenuous exercise, malnutrition, or lead poisoning, gout, renal disorders, increased breakdown of body cells
in some cancers (including leukemia, lymphoma, and multiple myeloma) or cancer treatments, hemolytic anemia, sickle cell

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 8 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 06:22PM
Sample Type : Serum Report Status : Final Report

BIOCHEMISTRY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
anemia, or heart failure, pre-eclampsia, liver disease (cirrhosis), obesity, psoriasis, hypothyroidism, low blood levels of
parathyroid hormone (PTH), certain drugs, foods that are very high in purines - such as organ meats, red meats, some seafood
and beer. Decreased levels are seen in liver disease, Wilson's disease, Syndrome of inappropriate antidiuretic hormone (SIADH),
certain drugs.

Calcium
Calcium 9.5 mg/dL 8.4-10.2 Arsenazo III

Comment:
Increased in: Hyperparathyroidism primary and secondary, Acute and chronic renal failure, Following renal transplantation,
Osteomalacia with malabsorption, Acute osteoprosis, Malignant tumours (specially of breast, lung and kidney), Drugs: Vit. D and
A intoxication, Diuretics, estrogen, androgen, tamoxifen, lithium

Decreased in: Hypoparathyroidism, Surgical and Idiopathic, Pseudohypoparathyroidism, Chronic renal disease with uremia and
phophate retention, Malabsorption of Calcium and Vit.D, obstructive jaundice, Bone Disease ( Osteomalacia and rickets), Drugs:
Cancer chemotherapy drugs, calcitonin, loop-actives diuretics, Hypomagnesemia,Hypoalbuminemia

High Sensitive CRP

High sensitivity CRP 0.93 mg/L <1.0 - Low Risk Turbidimetry
1.0 - 3.0 Average risk
>3.0 High Risk

Comment:
High Sensitivity C- Reactive protein (hs-CRP)is used as a marker for determining and performing risk assessment of
cardiovascular disease (good marker for inflammation), often along with tests for Lipid profile.
The American Heart Association and US Centers for Disease Control and Prevention have defined risk groups as follows:

<1.0 Low Risk

1.0 - 3.0 - Average Risk
>3.0 High Risk

These values are only a part of the total evaluation process for cardiovascular diseases.
To assess vascular risk ,it is recommended to test hsCRP levels 2 or more weeks apart and calculate the average

Additional risk factors to be considered are elevated levels of lipids & glucose, smoking, high blood pressure (hypertension).
Anti inflammatory drugs (like aspirin, ibuprofen, and naproxen) or statins may reduce CRP levels in blood. It is important that any
person undergoing this test must be in a healthy state in order for the results to be of diagnostic value in predicting the risk of
coronary artery disease or heart attack. Any recent illness, tissue injury, infection, or other general inflammation will raise the
amount of hsCRP and give a falsely elevated estimate of risk.
Women on hormone replacement therapy have been shown to have elevated hs-CRP levels.

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 9 of 17
PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 06:22PM
Sample Type : Serum Report Status : Final Report

BIOCHEMISTRY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
Note:
Since the hs-CRP and CRP tests measure the same molecule, people with chronic inflammation, such as those with arthritis,
should not have hs-CRP levels measured. Their CRP levels will be very high due to the arthritis/often too high to be measured or
meaningful using the hs-CRP test.

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 10 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 04:40PM
Sample Type : Serum Report Status : Final Report

IMMUNOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

Thyroid Stimulating Hormone, Ultrasensitive

Thyroid Stimulating Hormone - Ultra 2.429 µIU/mL 0.35-4.94 CMIA
Sensitive

Comment:

Reference ranges for TSH (μIU/ml) [As per American thyroid

Pregnancy
Association]
1st
0.1-2.5
trimester
2nd
0.2-3.0
trimester
3rd
0.3-3.0
trimester

TSH levels are subject to circadian variation, reaching peak levels between 2 - 4.a.m. and at a minimum between 6-10 pm
.
The variation is of the order of 50%, hence time of the day has influence on the measured serum TSH concentrations.
TSH is secreted in a dual fashion: Intermittent pulses constitute 60-70% of total amount, background continuous secretion
is 30-40%.These pulses occur regularly every 1-3 hrs.
TSH is a very sensitive and specific parameter for assessing thyroid function and is particularly suitable for early detection
or exclusion of disorders in the central regulating circuit between the hypothalamus, pituitary and thyroid.
Changes in thyroid status are typically associated with concordant changes in T3, T4 and TSH levels.
For the diagnosis of hypothyroidism and hyperthyroidism, sole dependence on TSH should not be done and assay needs
to be interpreted with the clinical condition & other investigations.
Serum TSH level changes significantly in response to even minor changes in thyroid hormones.
Transient increase in TSH level or an abnormal TSH levels can be seen in various nonthyroidal diseases.
Unexpectedly abnormal or discordant thyroid test values may be seen with some rare, but clinically significant conditions
such as central hypothyroidism, TSH-secreting pituitary tumors, thyroid hormone resistance, or the presence of
heterophilic antibodies (HAMA) or thyroid hormone autoantibodies.

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 11 of 17
PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 04:40PM
Sample Type : Serum Report Status : Final Report

IMMUNOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
TSH T3 T4 Interpretation
High Normal Normal Subclinical Hypothyroidism
Low Normal Normal Subclinical Hyperthyroidism
High High High Secondary Hyperthyroidism
Low High/Normal High/Normal Hyperthyroidism
Non thyroidal illness / Secondary
Low Low Low
Hypothyroidism

Free T4 1.17 ng/dL 0.7-1.48 CMIA

Comment:

Below mentioned are the guidelines for pregnancy related reference ranges for free T4.

Pregnancy Reference Ranges(ng/dL)

1st trimester 0.7-2.0
2nd trimester 0.5-1.6
3rd trimester 0.5-1.6

FT4 is the biologically active fraction of thyroxine in circulating blood.

In patients with hyperthyroidism, the FT4 concentration increases, whereas in patients with hypothyroidism it generally
decreases.
Patients on hormone replacement therapy may have an elevation of FT4, although clinically they are euthyroid.
The determination of free T4 has the advantage of being independent of changes in the concentrations and binding
properties of the binding proteins.
For diagnostic purposes, the results should always be assessed in conjunction with the patient’s medical history, clinical
examination and other findings.

TSH T3 /FT3 T4/FT4 Interpretation

High Normal Normal Subclinical Hypothyroidism
Low Normal Normal Subclinical Hyperthyroidism

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 12 of 17
PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 04:40PM
Sample Type : Serum Report Status : Final Report

IMMUNOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
High High High Secondary Hyperthyroidism
Low High/Normal High/Normal Hyperthyroidism
Non thyroidal illness / Secondary
Low Low Low
Hypothyroidism

Free T3 3.01 pg/mL 1.58-3.91 CMIA

Comment:

Below mentioned are the guidelines for pregnancy related reference ranges for free T3.

Pregnancy Reference Ranges(pg/mL)

1st trimester 2.0-3.8
2nd trimester 2.0-3.8
3rd trimester 2.0-3.8

Free T3 measurements support the differential diagnosis of thyroid disorders, are needed to distinguish different forms of
hyperthyroidism, to identify patients with T3 thyrotoxicosis, monitoring of patients with hypothyroidism treated with
Thyroxine and antithyroid agents.
The determination of free T3 has the advantage of being independent of changes in the concentrations and binding
properties of the binding proteins.
For diagnostic purposes, the results should always be assessed in conjunction with the patient’s medical history, clinical
examination and other findings.

TSH T3 /FT3 T4/FT4 Interpretation

High Normal Normal Subclinical Hypothyroidism
Low Normal Normal Subclinical Hyperthyroidism
High High High Secondary Hyperthyroidism
Low High/Normal High/Normal Hyperthyroidism
Non thyroidal illness / Secondary
Low Low Low Hypothyroidism

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 13 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 04:40PM
Sample Type : Serum Report Status : Final Report

IMMUNOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

Vitamin D (25-OH)
Vitamin D (25-OH) 5.5 ng/mL Deficiency:< 20, CMIA
Insufficiency:20-29,
Sufficiency:30-100,
Hypervitaminosis:> 100
Note: Kindly correlate with clinical history, diet, supplements and exposure to sunlight

Comment:

Vitamin D is a fat-soluble steroid prohormone involved in the intestinal absorption of calcium and the regulation of calcium
homeostasis.
Two forms of vitamin D are biologically relevant - vitamin D3 (Cholecalciferol) and vitamin D2 (Ergocalciferol).
Both vitamins D3 and D2 can be absorbed from food but only an estimated 10-20perc. of vitamin D is supplied through
nutritional intake.
Vitamin D is converted to the active hormone 1,25-(OH)2-vitamin D (Calcitriol) through two hydroxylation reactions. The
first hydroxylation converts vitamin D into 25-OH vitamin D and occurs in the liver. The second hydroxylation converts 25-
OH vitamin D into the biologically active 1,25-(OH)2-vitamin D and occurs in the kidneys as well as in many other cells of
the body.
Most cells express the vitamin D receptor and about 3perc. of the human genome is directly or indirectly regulated by the
vitamin D endocrine system.
The major storage form of vitamin D is 25-OH vitamin D and is present in the blood at up to 1,000 fold higher
concentration compared to the active 1,25-(OH)2-vitamin D. 25-OH vitamin D has a half-life of 2-3 weeks vs. 4 hours for
1,25-(OH)2-vitamin D. Therefore, 25-OH vitamin D is the analyte of choice for determination of the vitamin D status.
Risk factors for vitamin D deficiency include low sun exposure, inadequate intake, decreased absorption, abnormal
metabolism, vitamin D resistance and and liver or kidney diseases.
Vitamin D deficiency is a cause of secondary hyperparathyroidism and diseases resulting in impaired bone metabolism (like
rickets, osteomalacia).
Recently, many chronic diseases such as cancer, high blood pressure, osteoporosis and several autoimmune diseases
have been linked to vitamin D deficiency.
The assay measures both D2 (Ergocalciferol) and D3 (Cholecalciferol) metabolites of vitamin D

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 14 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022823 / 12708591 Report Date : 30/Apr/2025 04:40PM
Sample Type : Serum Report Status : Final Report

IMMUNOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
Utility Quantitative determination of 25-hydroxyvitamin D (25-OH vitamin D).

Vitamin B12
Vitamin B12 171.0 pg/mL 187-833 CMIA

Comment:

Vitamin B12 along with folate is essential for DNA synthesis and myelin formation.
Decreased levels a r e s e e n i n a n a e m i a , t e r m p r e g n a n c y , v e g e t a r i a n d i e t , i n t r i n s i c f a c t o r d e f i c i e n c y , p a r t i a l
gastrectomy/ileal damage, celiac disease, oral contraceptive use, parasitic infestation, pancreatic deficiency, treated
epilepsy, smoking, hemodialysis and advanced age.
Increased levels are seen in renal failure, hepatocelluar disorders, myeloproliferative disorders and at times with excess
supplementation of vitamins pills.

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 15 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022826 / 12708591 Report Date : 30/Apr/2025 03:50PM
Sample Type : Urine Report Status : Final Report

CLINICAL PATHOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method

Urine Routine & Microscopy

Urine Routine & Microscopy
Colour Pale Yellow Pale Yellow
Appearance Clear Clear Visual
Specific gravity 1.010 1.003 - 1.035 pKa change
pH 6.5 4.6 - 8.0 Double Indicator
Glucose Negative Negative GOD-POD
Protein Negative Negative Protein Error Principle
Ketones Negative Negative Nitroprusside
Blood Negative Negative Peroxidase
Bilirubin Negative Negative Diazonium
Urobilinogen Normal Normal Ehrlich
Leucocyte Esterase Negative Negative Pyrrole
Nitrite Negative Negative Diazonium Compound
Pus cells 2-4 /hpf 0-5 Microscopy
Red Blood Cells Nil /hpf 0-2 Microscopy
Epithelial cells 1-2 /hpf Few Microscopy
Casts Nil /lpf Nil Microscopy
Crystals Nil Nil Microscopy
Yeast Nil Nil Microscopy
Bacteria Nil Nil Microscopy

Comment:
•Note: Pre-test condition to be observed while submitting the sample-first void, mid stream urine, collected in a clean, dry, sterile
container is recommended for routine urine analysis, avoid contamination with any discharge from vaginal, urethra, perineum,
Avoid prolonged transit time & undue exposure to sunlight.
•During interpretation, points to be considered are Negative nitrite test does not exclude the urinary tract infections. Trace
proteinuria can be seen with many physiological conditions like prolonged recumbency, exercise, high protein diet. False positive
reactions for bile pigments, proteins, glucose and nitrites can be caused by peroxidase like activity by disinfectants, therapeutic
dyes, ascorbic acid and certain drugs.• Urine microscopy is done in centrifuged urine specimens

*** End Of Report ***

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 16 of 17
 PO No :Pjhgsda876sd

Name : Mr.KETAN GAIKWAD Client Name : TATA 1MG BANGALORE

Age/Gender : 30/Male Referred By : Dr.
Patient ID : MGB1198397 Collection Date : 30/Apr/2025 07:12AM
Barcode ID/Order ID : D20022826 / 12708591 Report Date : 30/Apr/2025 03:50PM
Sample Type : Urine Report Status : Final Report

CLINICAL PATHOLOGY
TRUWORTH VBCHOME
Test Name Result Unit Bio. Ref. Interval Method
Conditions of Laboratory Testing & Reporting:
Test results released pertain to the sample, as received. Laboratory investigations are only a tool to facilitate in arriving at a diagnosis and should
be clinically correlated by the interpreting clinician. Result delays may happen because of unforeseen or uncontrollable circumstances. Test report
may vary depending on the assay method used. Test results may show inter-laboratory variations. Test results are not valid for medico-legal
purposes. Please mail your queries related to test results to Customer Care mall ID care@1mg.com

Disclaimer: Results relate only to the sample received. Test results marked "BOLD" indicate abnormal results i.e. higher or lower than normal. All
lab test results are subject to clinical interpretation by a qualified medical professional. This report cannot be used for any medico-legal purposes.
Partial reproduction of the test results is not permitted. Also, TATA 1mg Labs is not responsible for any misinterpretation or misuse of the
information. The test reports alone may not be conclusive of the disease/condition, hence clinical correlation is necessary. Reports should be
vetted by a qualified doctor only.

This test has been performed at

TATA 1MG BANGALORE
Address: No 607, Ground, 1st & 2nd Floor, 80
Feet Road, 6th Block, Koramangala,
Bengaluru, 560095

Page 17 of 17
 Ensuring accuracy IN every single report
Following a 3-step review process:

Advanced systems & Experienced lab experts Each report undergoes

cutting-edge technology analyze and technicians conduct rigorous medical scrutiny & is
results with precision comprehensive reviews signed off by a doctor

Have concerns regarding the report?

Reach out to our care team at care@1mg.com
or chat with us
CONNECT NOW >

Accurate Testing, Assured Quality: Diagnostics Precision

Stringent quality control Cutting-edge technology Experienced lab staff

Measures meeting Robust healthcare systems 30+ medical professionals
international norms of safety equipped with calibrated & with a collective
guidelines well-maintained machinery experience of 200+ years

Verified test procedures External assessments Trained phlebotomists

Highly standardized test Thorough third-party Ensuring smooth sample
procedures following CLSI* assessment by authorized collection experience &
guidelines experts pre-analytical precision

Claim FREE doctor consultation

Watch how
Consult top doctors from
the comfort of your home
we take care of
your sample
SCHEDULE NOW>

Get Second Opinion Order Medicines EXPLORE NOW >

Explore Financial Need Help?

Book Lab Tests
Support & more 1800-102-1618

*Clinical & Laboratory Standards Institute T&C Apply

 Running Low on Vitamin D?
Choose clinically proven , ready-to-drink1
Vitamin D3 with 34% better absorption2

34% Better Absorption*2

Palatable Taste1

Sugar Free1

LIMITED OFFER

MAT-IN-2500204 v1.0 02/25

*With DePURA, 34% higher Vitamin D3 levels are achieved as compared to
conventional formulation.
Reference: 1. Data on File 2. Marwaha, Raman K., et al. "Efficacy of micellized
vs. fat-soluble vitamin D3 supplementation in healthy school children from
20 % OFF
ON TATA 1MG
SHOP NOW!
use code:
DEP20
Northern India."Journal of Pediatric Endocrinology and Metabolism 29.12.

Are you getting

enough OMEGA 3

^ Stark KD, et al, progress in Lipid Research 2016

* Compared with competing products
to protect your heart?
Because 80%^ of people don’t!
# Optimal requirement of Omega-3 as mentioned by National Institutes
+ Reference from NCBI published article on comparative bioavailability

Choose Tata 1mg Salmon Omega 3 of Health. Dietary Supplement Label Database. 2015.

LDL

Reduces Improves Reduces

Triglyceride Levels Good Cholesterol Inflammation

Why Choose Us?

50% Higher Absorption+
with Triglyceride form 50% Lower
Saturated Fats*
Every batch
Tested and Certified

Upto 30% off Shop Now