Patient Name : MRS.
ALKA Reg Date : 15/08/2025
Age & Sex : 25 Years & Female Report Date : 15/08/2025
Referred By : DR. HAYAT HOSPITAL Reg No : 3163
Lab Name : OM PATH LAB (9467742664) Sample ID :
3163
Complete Blood Count (CBC)
Test Description Result Unit Reference Range
Hemoglobin (Hb) 10.9 g/dl 11.0 - 15.0
Method: Colorimetric Non Cyanide
R.B.C Count 3.51 mil./cmm 3.8 - 4.8
Method: Electric Impedance
Packed Cell Volume (HCT) 32.0 % 36.0 - 46.0
Method: Electric Impedance
Mean Cell Volume (MCV) 91.17 fL 83.0 - 101.0
Method: Calculated
Mean Cell Haemoglobin (MCH) 31.05 Picogram 27.0 - 33.0
Method: Calculated
Mean Corpuscular Hb Concn. (MCHC) 34.06 g/dl 32.0 - 38.0
Method: Calculated
Red Cell Distribution Width(RDW) 13.2 % 11.60 - 14.0
Method: Electric Impedance
Total Leucocyte Count(TLC) 3.1 thou/mm3 4.0 - 11.0
Method: Electric Impedance
Differential Leucocyte Count(DLC)
Segmented Neutrophil 66 % 45 - 75
Method: SF Cube Technology
Lymphocytes 29 % 20 - 40
Method: SF Cube Technology
Eosinophil 02 % 1-6
Method: SF Cube Technology
Monocytes 03 % 2 - 10
Method: SF Cube Technology
Basophils 00 % 0-2
Method: SF Cube Technology
Absolute Differential Count
Absolute Neutrophil Count 2.05 thou/mm3 2.00 - 7.00
Method: Calculated
Absolute Lymphocyte Count 0.90 thou/mm3 1.00 - 3.00
Method: Calculated
Absolute Eosinophils Count 0.06 thou/mm3 0.10 - 0.50
Method: Calculated
Absolute Monocyte Count 0.09 thou/mm3 0.20 - 1.00
Method: Calculated
Absolute Basophils Count 0.00 thou/mm3 0.00 - 0.10
Method: Calculated
Platelet Count 124 thou/mm3 150 - 450
Method: Electric Impedance/Manual
Page 1 of 6
Patient Name : MRS. ALKA Reg Date : 15/08/2025
Age & Sex : 25 Years & Female Report Date : 15/08/2025
Referred By : DR. HAYAT HOSPITAL Reg No : 3163
Lab Name : OM PATH LAB (9467742664) Sample ID :
3163
Complete Blood Count (CBC)
Test Description Result Unit Reference Range
Mean Platelet Volume (MPV) 16.3 fL 7.2 - 11.7
Method: Electric Impedance
**END OF REPORT**
Dr. BALENDRA SINGH SODHI
(CONSULTANT PATHOLOGIST)
Page 2 of 6
Patient Name : MRS. ALKA Reg Date : 15/08/2025
Age & Sex : 25 Years & Female Report Date : 15/08/2025
Referred By : DR. HAYAT HOSPITAL Reg No : 3163
Lab Name : OM PATH LAB (9467742664) Sample ID :
3163
PBS MALARIAL PARASITE
Test Description Result Unit Reference Range
Malaria Parasite Not Detected Not Detected
Method: (microscopy)
Note:
Microscopic methods of detection may miss low levels of [Link] case of strong index of clinical
suspicion, serologic test for malaria may be performed.
**END OF REPORT**
Dr. BALENDRA SINGH SODHI
(CONSULTANT PATHOLOGIST)
Page 3 of 6
Patient Name : MRS. ALKA Reg Date : 15/08/2025
Age & Sex : 25 Years & Female Report Date : 15/08/2025
Referred By : DR. HAYAT HOSPITAL Reg No : 3163
Lab Name : OM PATH LAB (9467742664) Sample ID :
3163
WIDAL SLIDE AGGLUTINATION TEST
Test Description Result Unit Reference Range
Widal test (Serum)
(Method: Slide Agglutination)
Salmonella Typhi ‘O’ Agglutination 1:160 No Agglutination
Salmonella Typhi ‘H’ Agglutination 1:80 No Agglutination
Salmonella Paratyphi A(H) No Agglutination No Agglutination
Salmonella Paratyphi B(H) No Agglutination No Agglutination
Test Information
Agglutination titer greater than 1:80 is considered significant.
The past history of enteric fever or inoculation of vaccine can interfere with the result.
Clinical significance:
1. The organism Salmonella typhi is responsible for causing enteric fever/typhoid fever, which is
characterized by high consistent fever, loss of appetite, transitory bacteremia, round or oval-shaped ulcers
on the smooth peritoneal surface of Peyer's patches, etc.
2. The organism possesses an 'O' antigen on the cell wall and 'H' antigen on its flagella, against which the
host body produces immunospecific antibodies.
3. Paratyphoid fever caused by Salmonella paratyphi A or B is characterized by a milder course of the
disease.
4. These organisms also possess somatic 'O' and flagellar antigen termed as A(H) and B (H) respectively
**END OF REPORT**
Dr. BALENDRA SINGH SODHI
(CONSULTANT PATHOLOGIST)
Page 4 of 6
Patient Name : MRS. ALKA Reg Date : 15/08/2025
Age & Sex : 25 Years & Female Report Date : 15/08/2025
Referred By : DR. HAYAT HOSPITAL Reg No : 3163
Lab Name : OM PATH LAB (9467742664) Sample ID :
3163
C-REACTIVE PROTEIN;CRP
Test Description Result Unit Reference Range
C-REACTIVE PROTEIN;CRP 17.30 mg/L UP TO 6 mg/L
Nephelometry
Interpretation :
CRP is an acute phase reactant which is used in inflammatory disorders for monitoring course and effect
of therapy. It is most useful as an indicator of activity in Rheumatoid arthritis, Rheumatic fever, tissue
injury or necrosis and infections. As compared to ESR, CRP shows an earlier rise in inflammatory
disorders which begins in 4-6 hrs, the intensity of the rise being higher than ESR and the recovery being
earlier than [Link] ESR, CRP levels are not influenced by hematologic conditions like Anemia,
Polycythemia etc.
**END OF REPORT**
Dr. BALENDRA SINGH SODHI
(CONSULTANT PATHOLOGIST)
Page 5 of 6
Patient Name : MRS. ALKA Reg Date : 15/08/2025
Age & Sex : 25 Years & Female Report Date : 15/08/2025
Referred By : DR. HAYAT HOSPITAL Reg No : 3163
Lab Name : OM PATH LAB (9467742664) Sample ID :
3163
Dengue Ns1 Anti-gen
Test Description Result Unit Reference Range
Dengue NS1 Antigen Positive Negative
Method: "Sandwich" Immunoassay
Test information
Recommended test is NS1 Antigen in the first 5 days of fever. After 7-10 days of fever, the recommended
test is Dengue fever antibodies IgG & IgM.
Comments
Dengue viruses belong to the family Flaviviridae and have 4 subtypes (1-4). Dengue virus is transmitted by
the mosquito Aedes aegypti and Aedes albopictus, widely distributed in Tropical and Subtropical areas of
the world. Dengue is considered to be the most important arthropod borne viral disease due to the human
morbidity and mortality it causes. The disease may be subclinical, self limiting, febrile or may progress to
a severe form of Dengue hemorrhagic fever or Dengue shock syndrome.
**END OF REPORT**
Dr. BALENDRA SINGH SODHI
(CONSULTANT PATHOLOGIST)
Page 6 of 6
