List of top Questions asked in GPAT

Minimum manufacturing space for 'Habb-Unani medicine' as per Schedule of D and C Act?
How much volume of Raw spirit can an excise officer withdraw as sample?
Chikusetsu saponin is present in:
Partial hydrogenation of vegetable oils in the presence of Ni catalyst at 200°C gives:
Enzyme commonly targeted by drugs to treat hypertension is:
The biological name of Indian Bdellium is:
Size of a pilot plant batch is:
Enzyme commonly targeted by drugs to treat hypertension is:
Etoposide and Teniposide are the semi-synthetic derivatives of:
Match the following disease with their test for detection:
DiseaseDiagnostic tests
P.Tuberculosis(i)Lepromin test
Q.AIDS(ii)ELISA
R.Syphilis(iii)Mantoux test
S.Leprosy(iv)Kahn's test
The fluoroquinolones act by:
Match the following antibodies with their correct description:
AntibodyDescription
P. IgE(i) Cross the placenta
Q. IgG(ii) Dominant antibody produced in immune responses
R. IgM(iii) It is found in the mother's milk
S. IgA(iv) Responsible for autoimmune responses including allergies
The fluoroquinolones act by:
Tetracycline undergoes epimerization at C4 between pH 4-8 to give:
Which of the following drug does NOT require therapeutic drug monitoring:
Which ring of warfarin is essential for its therapeutic activity:
Which of the following drug does NOT require therapeutic drug monitoring:
In a homologous series of any general anesthetic, increasing the chain length increases the lipid solubility and produces a corresponding increase in anesthetic potency, is proposed by:
5-Fluorouracil, an anti-metabolite used in cancer treatment, is activated to:
Examples of BCS class III drugs are:
Examples of BCS class III drugs are:
Which ring of warfarin is essential for its therapeutic activity:
5-Fluorouracil, an anti-metabolite used in cancer treatment, is activated to:
In a homologous series of any general anesthetic, increasing the chain length increases the lipid solubility, and produce a corresponding increase in anesthetic potency, is proposed by:
Tetracycline undergoes epimerization at C4 between pH 4-8 to give: