Q. Multiple dose study is better since we can understand the peak, valley, drug blood levels, etc.

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Q. Which of the following is the pharmacodynamics method of studying bioavailability?

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Q. Which of the following is not an important parameter of plasma level time studies?

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Q. What is the equation for bioavailability?

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Q. The urinary excretion of the unchanged drug is directly proportional to the plasma concentration of a drug.

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Q. Which of the following will not be a parameter that should be examined for urinary excretion data?

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Q. Which of the following is not measured in acute pharmacological response study?

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Q. Therapeutic response is based on observing the clinical response to a drug formulation.

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Q. In vitro determination of bioavailability by dissolution rate is not the best way to determine therapeutic efficacy.

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Q. What is bioequivalence?

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Q. What is the chemical equivalence?

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Q. What is pharmaceutic equivalence?

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Q. What is bioequivalence?

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Q. What is therapeutic equivalence?

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Q. On which individuals study of newly invented medicines are not done?

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Q. What should be the disadvantage of cross over study on volunteers?

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Q. Two or more drugs contain the same therapeutically active ingredient which elicits same pharmacological effects and can control the disease to the same extent are known to be pharmaceutic equivalent.

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Q. If the bioavailability of test formulation is 80-120% of the reference standard, it is considered to be bioequivalent.

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Q. Bioequivalence is a relative term which denotes that the drug substance reaches the systemic circulation at the same relative rate or time.

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Q. Poor bioavailability means poor aqueous solubility.

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