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Biopharmaceutics and Pharmacokinetics
List of top Biopharmaceutics and Pharmacokinetics Questions on Bio-pharmaceutics
Histogram can be drawn only for:
GPAT - 2024
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Which of the following is an example of physical incompatibility:
GPAT - 2024
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Which of the following is true for bone tissue cell differentiation and maturation?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
A hypertensive patient receiving a drug ‘Y’for managing BP was prescribed a tricyclic antidepressant. As a result, there was an abolition of the antihypertensive action of‘Y’. Which of the following drug could be ‘Y’?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
A 70 kg woman was administered 1000 mg of the drug as i.v. bolus. After its uniform distribution in the body, the plasma concentration of the drug was found to be 50 mg/L. What is its volume of distribution?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Which of the following levels of IVIVC is represented by “the relatinship between one dissolution time point(e.g., t 50%) and one mean pharmacokinetic parameter, such as AUC, T
max
or C
max
”?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
In pharmacokinetic models, the term “compartment” means:
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Method of Study Drug Distribution pattern is:
GPAT - 2020
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
For drug substances with highly variable pharmacokinetic characteristics the following Bioequivalence study design is used
GPAT - 2019
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
IVIVC utilizes the principles of statistical moment analysis:-
GPAT - 2018
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
When Ke is constant and Ka is larger:-
GPAT - 2018
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
In relation to buccal and sublingual route of administration which of the following statement is incorrect
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Diazepam is not suitable for peroral sustained release form since
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Apparent volume of distribution will be highest in case of the drug with % plasmaprotein binding
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
(Weight in pounds/150)* Adult Dose = Child dose. The above formula is known as________in Posology
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Bioavailability differences among drug's oral formulations are most likely to occur if it
GPAT - 2016
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Method of inspections used to determine the absorption rate constants. It assumes that
(P) Ka is at least five time grater activities
(Q) Absorption in complete (i.e. > 95% complete) at the time of peak concentration
(R) Both Absorption and elimination are first order processes
GPAT - 2016
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
What does 'pharmacokinetical compartment' mean
GPAT - 2016
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Conc v/s time curve drown from single oral dose, which parameter can be calculated
GPAT - 2015
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Characteristics feature if hemorrhagic dengue fever is
GPAT - 2015
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Which of the following are the correct properties of ferroin? Ferroin is(P) 1, 10-phnathroline
(Q) A bidentate ligand complex
(R) Red in reduced form
(S) Blue in oxidized form
GPAT - 2015
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Which of the first drugs are potentiated by the second
GPAT - 2015
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Passive diffusion follows which order of kinetics
GPAT - 2015
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
If a basic drug reabsorbed significantly from kidney which of the following statement will be correct
GPAT - 2015
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
The loading dose (DL) of a drug is usually based on the:
GPAT - 2015
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
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