Non-steroidal anti-inflammatory drugs (NSAIDs) — clinical effect and indication

Abstract

They are subject to common properties and these properties are very similar among different NSAIDs. After NSAID administration, relief of pain, stiffness and other symptoms occurs. Individual variations in the effectiveness of a particular NSAID can be explained by the pharmacokinetics of the drug at the cellular level. Various factors such as physical and chemical properties of the drug, pharmacokinetic parameters, the ability to inhibit a particular isoform of cyclooxygenase, selection of the form of application and the variability of the treated disease or symptom, all affect the variability of NSAID effectiveness (see table 6).
Table 6

Variability of NSAID effectiveness

Physical and chemical

Lipid solubility

properties

 

Pharmacokinetics

plasma half-life

Pharmacodynamics

selectivity of COX-2

 

inhibition

Dose selection and

chronopharmacology

application period

 

Variability of disease

elimination organ

 

disorders

Adverse effects,

idiosyncrasy

pharmacogenetic

 

differences

 

Keywords

Patent Ductus Arteriosus Mefenamic Acid Anthranilic Acid Reactive Arthritis Tiaprofenic Acid 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Copyright information

© Springer-Verlag/Wien 2009

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