Report AL182C77837807491833 2023 07 07 R L

PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,
Gomti Nagar, Lucknow – 226 010
NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

REF. BY KANPUR UTTAR PRADESH KANPUR - 208001
: SELF
TEST ASKED : AAROGYAM C PRO WITH UTSH
PATIENTID : GG15114674
TEST NAME TECHNOLOGY VALUE UNITS
25-OH VITAMIN D (TOTAL) C.L.I.A 85.84 ng/mL

Reference Range :
DEFICIENCY : <20 ng/ml || INSUFFICIENCY : 20-<30 ng/ml
SUFFICIENCY : 30-100 ng/ml || TOXICITY : >100 ng/ml
Clinical Significance:
Vitamin D is a fat soluble vitamin that has been known to help the body absorb and retain calcium and phosphorous; both are critical
for building bone health. Decrease in vitamin D total levels indicate inadequate exposure of sunlight, dietary deficiency, nephrotic
syndrome. Increase in vitamin D total levels indicate Vitamin D intoxication.
Specifications: Precision: Intra assay (%CV):5.3%, Inter assay (%CV):11.9% ; Sensitivity:3.2 ng/ml.
Kit Validation Reference: Holick MF. Vitamin D Deficiency. N Engl J Med. 2007;357:266–81.
Method : FULLY AUTOMATED CHEMI LUMINESCENT IMMUNO ASSAY
VITAMIN B-12 C.L.I.A 357 pg/mL
Reference Range :
Normal : 211 - 911 pg/ml
Clinical significance :
Vitamin B12 or cyanocobalamin, is a complex corrinoid compound found exclusively from animal dietary sources, such as meat, eggs
and milk. It is critical in normal DNA synthesis, which in turn affects erythrocyte maturation and in the formation of myelin sheath.
Vitamin-B12 is used to find out neurological abnormalities and impaired DNA synthesis associated with macrocytic anemias. For
diagnostic purpose, results should always be assessed in conjunction with the patients medical history, clinical examination and
other findings.
Specifications: Intra assay (%CV):5.0%, Inter assay (%CV):9.2 %;Sensitivity:45 pg/ml
Kit Validation reference:

Chen IW, Sperling MI, Heminger LA. Vitamin B12. In: Pesce AJ, Kaplan LA, eds. Methods in Clinical Chemistry. St. Louis: CV Mosby;
1987:569–73.
Method : COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY
Please correlate with clinical conditions.
Sample Collected on (SCT) : 07 Jul 2023 20:28
Sample Received on (SRT) : 08 Jul 2023 02:14

Report Released on (RRT) : 08 Jul 2023 06:13
Sample Type : SERUM
Labcode : 0707110628/AL182 Dr.Shaffaly Gagneja MD (Path)
Barcode : AR952102
Page : 1 of 14
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

REF. BY : SELF KANPUR UTTAR PRADESH KANPUR - 208001
HIGH SENSITIVITY C-REACTIVE PROTEIN (HS-CRP) IMMUNOTURBIDIMETRY 3.96 mg/L
Reference Range :-
< 1.00 - Low Risk

1.00 - 3.00 - Average Risk
>3.00 - 10.00 - High Risk
> 10.00 - Possibly due to Non-Cardiac Inflammation
Disclaimer: Persistent unexplained elevation of HSCRP >10 should be evaluated for non-cardiovascular etiologies such as infection ,
active arthritis or concurrent illness.
Clinical significance:
High sensitivity C- reactive Protein ( HSCRP) can be used as an independent risk marker for the identification of Individuals at risk for
future cardiovascular Disease. A coronary artery disease risk assessment should be based on the average of two hs-CRP tests, ideally
taken two weeks apart.
Kit Validation Reference:

1.Clinical management of laboratory date in medical practice 2003-3004, 207(2003).
2.Tietz : Textbook of Clinical Chemistry and Molecular diagnostics :Second edition :Chapter 47:Page no.1507- 1508.

Method:- FULLY AUTOMATED LATEX AGGLUTINATION – BECKMAN COULTER

Sample Type : SERUM
Dr.Shaffaly Gagneja MD (Path)
Labcode : 0707110628/AL182
Barcode : AR952102 Page : 2 of 14
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

TESTOSTERONE C.L.I.A 20.01 ng/dL
Reference Range :-
Adult Male
21 - 49 Yrs : 164.94 - 753.38 || 50 - 89 Yrs : 86.49 - 788.22
Adult Female
Pre-Menopause : 12.09 - 59.46 || Post-Menopause: < 7.00 - 48.93
Boys
2-10 Years : < 7.00 - 25.91
11 Years : < 7.00 - 341.53
12 Years : < 7.00 - 562.59
13 Years : 9.34 - 562.93
14 Years : 23.28 - 742.46
15 Years : 144.15 - 841.44
16-21 Years : 118.22 - 948.56
Girls
2-10 Years : < 7.00 - 108.30
11-15 Years : < 7.00 - 48.40
16-21 Years : 17.55 - 50.41
Clinical Significance: Clinical evaluation of serum testosterone, along with serum LH, assists in evaluation of Hypogonadal males. Major
causes of lowered testosterone in males include Hypogonadotropic hypogonadism, testicular failure Hyperprolactinema,
Hypopituitarism some types of liver and kidney diseases and critical illness.
Specifications: Precision: Intra assay (%CV): 8.5 %, Inter assay (%CV): 12.6%; Sensitivity: 7 ng/dL.
Kit Validation Reference: Kicklighter EJ, Norman RJ. The gonads. In: Kaplan LA, Pesce AJ, eds. Clinical Chemistry: Theory, Analysis,
Correlation. 2nd ed. St. Louis: CV Mosby; 1989:657–662.

Method:- COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY

Sample Type : SERUM
Labcode : 0707110628/AL182
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

: SELF
IRON PHOTOMETRY 61.14 µg/dL

Reference Range :
Male : 65 - 175
Female : 50 - 170
Method : FERROZINE METHOD WITHOUT DEPROTEINIZATION
TOTAL IRON BINDING CAPACITY (TIBC) PHOTOMETRY 402.65 µg/dL
Reference Range :
Male: 225 - 535 µg/dl Female: 215 - 535 µg/dl
Method : SPECTROPHOTOMETRIC ASSAY
% TRANSFERRIN SATURATION CALCULATED 15.18 %
Reference Range :
13 - 45
Method : DERIVED FROM IRON AND TIBC VALUES
UNSAT.IRON-BINDING CAPACITY(UIBC) PHOTOMETRY 341.51 µg/dL
Reference Range :
162 - 368
Method : SPECTROPHOTOMETRIC ASSAY

Sample Type : SERUM
Barcode : AR952102
Page : 4 of 14
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

: SELF
TEST NAME TECHNOLOGY VALUE UNITS NORMAL RANGE
TOTAL CHOLESTEROL PHOTOMETRY 221 mg/dL < 200
HDL CHOLESTEROL - DIRECT PHOTOMETRY 58 mg/dL 40-60
HDL / LDL RATIO CALCULATED 0.43 Ratio > 0.40
LDL CHOLESTEROL - DIRECT PHOTOMETRY 135 mg/dL < 100
TRIG / HDL RATIO CALCULATED 1.79 Ratio < 3.12
TRIGLYCERIDES PHOTOMETRY 103 mg/dL < 150
TC/ HDL CHOLESTEROL RATIO CALCULATED 3.8 Ratio 3-5
LDL / HDL RATIO CALCULATED 2.3 Ratio 1.5-3.5
NON-HDL CHOLESTEROL CALCULATED 163.04 mg/dL < 160
VLDL CHOLESTEROL CALCULATED 20.65 mg/dL 5 - 40
Method :
CHOL - CHOLESTEROL OXIDASE, ESTERASE, PEROXIDASE
HCHO - DIRECT ENZYMATIC COLORIMETRIC
HD/LD - Derived from HDL and LDL values.
LDL - DIRECT MEASURE
TRI/H - Derived from TRIG and HDL Values
TRIG - ENZYMATIC, END POINT
TC/H - DERIVED FROM SERUM CHOLESTEROL AND HDL VALUES
LDL/ - DERIVED FROM SERUM HDL AND LDL VALUES
NHDL - DERIVED FROM SERUM CHOLESTEROL AND HDL VALUES
VLDL - DERIVED FROM SERUM TRIGLYCERIDE VALUES
*REFERENCE RANGES AS PER NCEP ATP III GUIDELINES:
TOTAL CHOLESTEROL (mg/dl) HDL (mg/dl) LDL (mg/dl) TRIGLYCERIDES (mg/dl)
DESIRABLE <200 LOW <40 OPTIMAL <100 NORMAL <150

BORDERLINE HIGH 200-239 HIGH >60 NEAR OPTIMAL 100-129 BORDERLINE HIGH 150-199
BORDERLINE HIGH
HIGH >240 130-159 HIGH 200-499
HIGH 160-189 VERY HIGH >500
VERY HIGH >190
Alert !!! 10-12 hours fasting is mandatory for lipid parameters. If not, values might fluctuate.

Sample Type : SERUM

PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

: SELF
ALKALINE PHOSPHATASE PHOTOMETRY 101.34 U/L 45-129
BILIRUBIN - TOTAL PHOTOMETRY 0.6 mg/dL 0.3-1.2
BILIRUBIN -DIRECT PHOTOMETRY 0.09 mg/dL < 0.3
BILIRUBIN (INDIRECT) CALCULATED 0.51 mg/dL 0-0.9
GAMMA GLUTAMYL TRANSFERASE (GGT) PHOTOMETRY 40.87 U/L < 38
SGOT / SGPT RATIO CALCULATED 1.08 Ratio <2
ASPARTATE AMINOTRANSFERASE (SGOT ) PHOTOMETRY 21.65 U/L < 31
ALANINE TRANSAMINASE (SGPT) PHOTOMETRY 20.1 U/L < 34
PROTEIN - TOTAL PHOTOMETRY 8.05 gm/dL 5.7-8.2
ALBUMIN - SERUM PHOTOMETRY 3.78 gm/dL 3.2-4.8
SERUM GLOBULIN CALCULATED 4.27 gm/dL 2.5-3.4
SERUM ALB/GLOBULIN RATIO CALCULATED 0.89 Ratio 0.9 - 2
Method :
ALKP - MODIFIED IFCC METHOD
BILT - VANADATE OXIDATION
BILD - VANADATE OXIDATION
BILI - DERIVED FROM SERUM TOTAL AND DIRECT BILIRUBIN VALUES
GGT - MODIFIED IFCC METHOD
OT/PT - Derived from SGOT and SGPT values.
SGOT - IFCC* WITHOUT PYRIDOXAL PHOSPHATE ACTIVATION
SGPT - IFCC* WITHOUT PYRIDOXAL PHOSPHATE ACTIVATION
PROT - BIURET METHOD
SALB - ALBUMIN BCG¹METHOD (COLORIMETRIC ASSAY ENDPOINT)
SEGB - DERIVED FROM SERUM ALBUMIN AND PROTEIN VALUES
A/GR - DERIVED FROM SERUM ALBUMIN AND PROTEIN VALUES

Sample Type : SERUM

PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

: SELF
UREA (CALCULATED) CALCULATED 47.57 mg/dL Adult : 17-43
BLOOD UREA NITROGEN (BUN) PHOTOMETRY 22.23 mg/dL 7.94 - 20.07
UREA / SR.CREATININE RATIO CALCULATED 51.71 Ratio < 52
CREATININE - SERUM PHOTOMETRY 0.92 mg/dL 0.55-1.02
BUN / SR.CREATININE RATIO CALCULATED 24.16 Ratio 9:1-23:1
CALCIUM PHOTOMETRY 9.42 mg/dL 8.8-10.6
URIC ACID PHOTOMETRY 6.38 mg/dL 3.2 - 6.1
SODIUM I.S.E 138.1 mmol/L 136 - 145
CHLORIDE I.S.E 98 mmol/L 98 - 107
Method :
UREAC - Derived from BUN Value.
BUN - KINETIC UV ASSAY.
UR/CR - Derived from UREA and Sr.Creatinine values.
SCRE - CREATININE ENZYMATIC METHOD
B/CR - DERIVED FROM SERUM BUN AND CREATININE VALUES
CALC - ARSENAZO III METHOD, END POINT.
URIC - URICASE / PEROXIDASE METHOD
SOD - ION SELECTIVE ELECTRODE
CHL - ION SELECTIVE ELECTRODE

Sample Type : SERUM

PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

KANPUR UTTAR PRADESH KANPUR - 208001
REF. BY : SELF
TEST NAME TECHNOLOGY VALUE UNITS REFERENCE RANGE
TOTAL TRIIODOTHYRONINE (T3) C.L.I.A 90 ng/dL 60-200

TOTAL THYROXINE (T4) C.L.I.A 8.6 µg/dL 4.5-12
TSH - ULTRASENSITIVE C.L.I.A 7.9 µIU/mL 0.55-4.78
Comments : ***
The Biological Reference Ranges is specific to the age group. Kindly correlate clinically.
Method :
T3 - COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY
T4 - COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY
USTSH - Third Generation Ultrasensitive Chemi Luminescent Immuno Assay
Disclaimer :Results should always be interpreted using the reference range provided by the laboratory that
performed the test. Different laboratories do tests using different technologies, methods and using different
reagents which may cause difference. In reference ranges and hence it is recommended to interpret result with
assay specific reference ranges provided in the reports. To diagnose and monitor therapy doses, it is recommended
to get tested every time at the same Laboratory.

Sample Type : SERUM
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

EST. GLOMERULAR FILTRATION RATE (eGFR) CALCULATED 70 mL/min/1.73 m2
Reference Range :-
> = 90 : Normal
60 - 89 : Mild Decrease
45 - 59 : Mild to Moderate Decrease
30 - 44 : Moderate to Severe Decrease
15 - 29 : Severe Decrease
Clinical Significance
The normal serum creatinine reference interval does not necessarily reflect a normal GFR for a patient. Because mild and moderate
kidney injury is poorly inferred from serum creatinine alone. Thus, it is recommended for clinical laboratories to routinely estimate
glomerular filtration rate (eGFR), a “gold standard” measurement for assessment of renal function, and report the value when serum
creatinine is measured for patients 18 and older, when appropriate and feasible. It cannot be measured easily in clinical practice,
instead, GFR is estimated from equations using serum creatinine, age, race and sex. This provides easy to interpret information for the
doctor and patient on the degree of renal impairment since it approximately equates to the percentage of kidney function remaining.
Application of CKD-EPI equation together with the other diagnostic tools in renal medicine will further improve the detection and
management of patients with CKD.
Reference
Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF, 3rd, Feldman HI, et al. A new equation to estimate glomerular filtration rate.
Ann Intern Med. 2009;150(9):604-12.

Method:- CKD-EPI Creatinine Equation

Sample Type : SERUM
Labcode : 0707110628/AL182
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

: SELF
TEST ASKED : HbA1c,HEMOGRAM
HbA1c - (HPLC)
H.P.L.C 5.7 %
Reference Range :
Reference Range: As per ADA Guidelines Guidance For Known Diabetics
Below 5.7% : Normal Below 6.5% : Good Control

5.7% - 6.4% : Prediabetic 6.5% - 7% : Fair Control
>=6.5% : Diabetic 7.0% - 8% : Unsatisfactory Control
>8% : Poor Control
Method : Fully Automated H.P.L.C method
AVERAGE BLOOD GLUCOSE (ABG) CALCULATED 117 mg/dL
Reference Range :
90 - 120 mg/dl : Good Control
121 - 150 mg/dl : Fair Control
151 - 180 mg/dl : Unsatisfactory Control
> 180 mg/dl : Poor Control
Method : Derived from HBA1c values

Sample Type : EDTA
Barcode : AV623309
Page : 10 of 14
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

TEST ASKED : HbA1c,HEMOGRAM
TEST NAME VALUE UNITS REFERENCE RANGE
TOTAL LEUCOCYTES COUNT (WBC) 9.36 X 10³ / µL 4.0 - 10.0
NEUTROPHILS 76.9 % 40-80
LYMPHOCYTE 18.9 % 20-40
MONOCYTES 2.4 % 2-10
EOSINOPHILS 1.3 % 1-6
BASOPHILS 0.2 % 0-2
IMMATURE GRANULOCYTE PERCENTAGE(IG%) 0.3 % 0.0-0.4
NEUTROPHILS - ABSOLUTE COUNT 7.2 X 10³ / µL 2.0-7.0
LYMPHOCYTES - ABSOLUTE COUNT 1.77 X 10³ / µL 1.0-3.0
MONOCYTES - ABSOLUTE COUNT 0.22 X 10³ / µL 0.2 - 1.0
BASOPHILS - ABSOLUTE COUNT 0.02 X 10³ / µL 0.02 - 0.1
EOSINOPHILS - ABSOLUTE COUNT 0.12 X 10³ / µL 0.02 - 0.5
IMMATURE GRANULOCYTES(IG) 0.03 X 10³ / µL 0.0-0.3
TOTAL RBC 4.86 X 10^6/µL 3.8-4.8
NUCLEATED RED BLOOD CELLS 0.01 X 10³ / µL 0.0-0.5
NUCLEATED RED BLOOD CELLS % 0.01 % 0.0-5.0
HEMOGLOBIN 12.3 g/dL 12.0-15.0
HEMATOCRIT(PCV) 45.1 % 36.0-46.0
MEAN CORPUSCULAR VOLUME(MCV) 92.8 fL 83.0-101.0
MEAN CORPUSCULAR HEMOGLOBIN(MCH) 25.3 pq 27.0-32.0
MEAN CORP.HEMO.CONC(MCHC) 27.3 g/dL 31.5-34.5
RED CELL DISTRIBUTION WIDTH - SD(RDW-SD) 56.7 fL 39.0-46.0
RED CELL DISTRIBUTION WIDTH (RDW-CV) 16.6 % 11.6-14.0
PLATELET COUNT 182 X 10³ / µL 150-410
Remarks : Alert!!! RBCs:Mild anisopoikilocytosis. Predominantly normocytic normochromic with ovalocytes. Platelets:Appear adequate in smear.
Please Correlate with clinical conditions.

Method : Fully automated bidirectional analyser (6 Part Differential SYSMEX XN-1000)
(This device performs hematology analyses according to the Hydrodynamic Focussing (DC method), Flow Cytometry Method
(using a semiconductor laser), and SLS- hemoglobin method)

Sample Type : EDTA
Barcode : AV623309 Page : 11 of 14
PROCESSED AT :
Thyrocare
CP-67, Viraj Khand,

TEST ASKED : BLOOD SUGAR (F)
FASTING BLOOD SUGAR(GLUCOSE) PHOTOMETRY 103.61 mg/dL
Reference Range :-
As per ADA Guideline: Fasting Plasma Glucose (FPG)
Normal 70 to 100 mg/dl
Prediabetes 100 mg/dl to 125 mg/dl
Diabetes 126 mg/dl or higher
Note :
The assay could be affected mildly and may result in anomalous values if serum samples have heterophilic antibodies, hemolyzed ,
icteric or lipemic. The concentration of Glucose in a given specimen may vary due to differences in assay methods, calibration and
reagent specificity. For diagnostic purposes results should always be assessed in conjunction with patients medical history, clinical
findings and other findings.
Method:- GOD-PAP METHOD
~~ End of report ~~

Sample Type : FLUORIDE
Labcode : 0707111025/AL182
Barcode : R1299583 Page : 12 of 14
CUSTOMER DETAILS
As declared in our data base
Name: MRS GEETA GUPTA Age: 55Y Sex: F
Barcodes/Sample_Type : R1299583 (FLUORIDE),AV623309 (EDTA),AR952102 (SERUM)

Labcode : 0707111025,0707111673,0707110628
Ref By : SELF
Sample_Type/Tests : FLUORIDE:FBS
EDTA:HBA , HEMOGRAM - 6 PART (DIFF)
SERUM:AAROGYAM C PRO WITH UTSH
Sample Collected At : KANPUR UTTAR PRADESH KANPUR - 208001

Amount Collected : Rs.1000/-(one thousand only)
Thyrocare,D-37/1,MIDC,Turbhe,Navi Mumbai - 400703. | Phone:022 - 6712 3400 |www.thyrocare.com | info@thyrocare.com
Page : 13 of 14
CONDITIONS OF REPORTING
v The reported results are for information and interpretation of the referring doctor only.
v It is presumed that the tests performed on the specimen belong to the patient; named or identified.
v Results of tests may vary from laboratory to laboratory and also in some parameters from time to time for the
same patient.
v Should the results indicate an unexpected abnormality, the same should be reconfirmed.
v Only such medical professionals who understand reporting units, reference ranges and limitations of technologies
should interpret results.
v This report is not valid for medico-legal purpose.
v Neither Thyrocare, nor its employees/representatives assume any liability, responsibility for any loss or damage
that may be incurred by any person as a result of presuming the meaning or contents of the report.
v Thyrocare Discovery video link :- https://youtu.be/nbdYeRgYyQc
v For clinical support please contact @8450950852,8450950853,8450950854 between 10:00 to 18:00
EXPLANATIONS
v Majority of the specimen processed in the laboratory are collected by Pathologists and Hospitals we call them
as "Clients".
v Name - The name is as declared by the client and recored by the personnel who collected the specimen.
v Ref.Dr - The name of the doctor who has recommended testing as declared by the client.
v Labcode - This is the accession number in our laboratory and it helps us in archiving and retrieving the data.
v Barcode - This is the specimen identity number and it states that the results are for the specimen bearing
the barcode (irrespective of the name).
v SCP - Specimen Collection Point - This is the location where the blood or specimen was collected as declared by
the client.
v SCT - Specimen Collection Time - The time when specimen was collected as declared by the client.
v SRT - Specimen Receiving Time - This time when the specimen reached our laboratory.
v RRT - Report Releasing Time - The time when our pathologist has released the values for Reporting.
v Reference Range - Means the range of values in which 95% of the normal population would fall.
SUGGESTIONS
v Values out of reference range requires reconfirmation before starting any medical treatment.
v Retesting is needed if you suspect any quality shortcomings.
v Testing or retesting should be done in accredited laboratories.
v For suggestions, complaints or feedback, write to us at info@thyrocare.com or call us on
022-3090 0000 / 6712 3400
v SMS:<Labcode No.> to 9870666333
Page : 14 of 14

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PROCESSED AT :

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

25-OH VITAMIN D (TOTAL) C.L.I.A 85.84 ng/mL

Normal : 211 - 911 pg/ml

Specifications: Intra assay (%CV):5.0%, Inter assay (%CV):9.2 %;Sensitivity:45 pg/ml

Kit Validation reference:

Sample Collected on (SCT) : 07 Jul 2023 20:28

Sample Received on (SRT) : 08 Jul 2023 02:14

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

TEST ASKED : AAROGYAM C PRO WITH UTSH

< 1.00 - Low Risk

Kit Validation Reference:

Please correlate with clinical conditions.

Sample Collected on (SCT) : 07 Jul 2023 20:28

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

TEST ASKED : AAROGYAM C PRO WITH UTSH

Please correlate with clinical conditions.

Sample Collected on (SCT) : 07 Jul 2023 20:28

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

IRON PHOTOMETRY 61.14 µg/dL

Sample Collected on (SCT) : 07 Jul 2023 20:28

Sample Received on (SRT) : 08 Jul 2023 02:14

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

DESIRABLE <200 LOW <40 OPTIMAL <100 NORMAL <150

Sample Collected on (SCT) : 07 Jul 2023 20:28

Barcode : AR952102 Page : 5 of 14

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

Sample Collected on (SCT) : 07 Jul 2023 20:28

Barcode : AR952102 Page : 6 of 14

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

Sample Collected on (SCT) : 07 Jul 2023 20:28

Barcode : AR952102 Page : 7 of 14

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

TEST NAME TECHNOLOGY VALUE UNITS REFERENCE RANGE

TOTAL TRIIODOTHYRONINE (T3) C.L.I.A 90 ng/dL 60-200

Sample Collected on (SCT) : 07 Jul 2023 20:28

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

TEST ASKED : AAROGYAM C PRO WITH UTSH

Please correlate with clinical conditions.

Sample Collected on (SCT) : 07 Jul 2023 20:28

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

Reference Range: As per ADA Guidelines Guidance For Known Diabetics

Below 5.7% : Normal Below 6.5% : Good Control

Sample Collected on (SCT) : 07 Jul 2023 20:28

Sample Received on (SRT) : 08 Jul 2023 02:35

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

Please Correlate with clinical conditions.

Sample Collected on (SCT) : 07 Jul 2023 20:28

NAME : MRS GEETA GUPTA (55Y/F) HOME COLLECTION :

TEST ASKED : BLOOD SUGAR (F)

As per ADA Guideline: Fasting Plasma Glucose (FPG)

Normal 70 to 100 mg/dl

Prediabetes 100 mg/dl to 125 mg/dl

Diabetes 126 mg/dl or higher

Sample Collected on (SCT) : 07 Jul 2023 20:28

As declared in our data base

Name: MRS GEETA GUPTA Age: 55Y Sex: F

Barcodes/Sample_Type : R1299583 (FLUORIDE),AV623309 (EDTA),AR952102 (SERUM)

Sample Collected on (SCT) : 07 Jul 2023 20:28