The loading dose of a drug is based upon the

Related MCQs

• ………………… is an initial higher dose of a drug that may be given at the beginning of a course of treatment before dropping down to a lower maintenance dose.
• Factors altering the binding of the drug to the blood increases the volume of distribution of the drug and the factors that influence drug binding to the extravascular component decreases the volume of distribution.
• Which of the following is a correct method to find the fraction of unbound drug in plasma? Given where Cu is the concentration of unbound drug and C is total plasma drug concentration.
• For a certain drug, the bile flow rate is 0.7 ml/mm, the biliary drug concentration is 2g/ml and the plasma drug concentration is 0.8g/ml. What will be the bile clearance?
• Multiple dose study is better since we can understand the peak, valley, drug blood levels, etc.
• …………………it is the extent to which a drug will accumulate relative to the first dose can be quantified by an accumulation factor R.
• In…………..Pharmacokinetic parameters for a drug can change with change in dose.
• …………..it is the extent to which a drug will accumulate relative to the first dose can be quantified by an accumulation factor R.
• If drug administered by Intravenous route appears in feaces, it implies that the drug
• If drug has pKa value of 3 then at pH value of 7 what would be the degree of ionisation of the drug?