Abstract
In personalized medicine, the appropriate drugs for an individual patient are selected based on the patient’s medical history, diagnostic testing,andgeneticinformationforthepurposeofminimizingdruginteractions(DIs),sideeffects,andadversedrugreactions(ADRs)and to obtain the maximum therapeutic beneï¬t. The DI is one of the major problems of pharmacotherapy, which perhaps leads to adverse outcome or therapeutic failure if not properly addressed. In clinical practice, patient safety is likely to improve through the identiï¬cation of frequently occurring DIs by pharmacist and notifying the other members of the health-care team. Recently, a software was introduced, which detects DIs with good precision; however, this software requires a constant update. Health-care professionals require adequate knowledge and skills on how to identify and avoid DIs to enable them complement the software assessment. Basically, DIs include drug–drug, drug–food, drug–herbal, and drug–disease interactions. These possibilities can be identiï¬ed from chemical properties, pharmacokinetics, and pharmacodynamics ofthedrug, patientmedical history, concomitant disease, ororgan failure. Focusing onDIswill help to reduce drug-related problems, advance the evidence-based medicine, and improve the level of patient satisfaction. Adequate knowledge of drug DIs will enable the health-care professionals to individualize the patient treatment in order to get maximum therapeuticbeneï¬t.ThisscriptisaimedatdescribingthevariousclassesofDIs,theircauses,andtheirimplications inclinicalpracticeand personalized medicine.