The pharmacokinetics of paracetamol are as follows. Oral bio availability (F)70%-90%, rectal bio availability 30%-70%, clearance 20 L/h, volume of distribution 65 L, and half life 2.5 hours.
Dennis A. Noe has written: 'A short course in clinical pharmacokinetics' -- subject(s): Pharmacokinetics
C. J. Hull has written: 'Pharmacokinetics for anaesthesia' -- subject(s): Analgesics, Anesthetics, Pharmacokinetics
Answer The word "pharmacokinetics" is used to describe a singular set of data, therefore it is written with a singular verb.
Susy Felix has written: 'Evaluating the pharmacokinetics of valproate in the elderly: dose-related changes and their influence on effects' 'Evaluating the pharmacokinetics of valproate in the elderly'
Pharmacokinetics refers to how the body processes a drug, including absorption, distribution, metabolism, and excretion. Pharmacodynamics, on the other hand, is the study of how a drug interacts with its target receptors or enzymes in the body to produce a biological response. In summary, pharmacokinetics deals with what the body does to the drug, and pharmacodynamics deals with what the drug does to the body.
Study of the distribution and removal of drugs in the body
By definition Pharmacokinetic is the branch of pharmacology deals with the liberation, absorption, distribution, metabolism and excretion of drugs. absorption, distribution, metabolism and excretion of drugs are primary four parameters of pharmacokinetics.
Butilhioscina-Paracetamol
Absorption Distribution Metabolism Excretion
phar-ma-co-ki-net-ics
Can paracetamol help heartburn
yes