Pharmacology is the laboratory analysis and creation of medications intended for medical use to treat diseases and other conditions safely and effectively. This goes well beyond the pharmacist standing at your typical drugstore counter. Though those professionals know a great deal about pharmacology, they may not be familiar with it in terms of clinical practice. In order for pharmacologists to better understand the effects of medications, physicians come onto the team to arrange formal trials to determine drug safety. All of this has to be involved to meet regulations and to make the most reliable and safe pharmaceutical compounds.
The clinical pharmacologist helps with drug development. Their clinical expertise is joined by the information from treating physicians in actual patient studies. Sometimes these studies may involve inpatient care while others may be done on an outpatient plan. Either way, medications are being studied for efficacy and safety within the safety of a clinical environment equipped to handle any outcomes. Clinical pharmacology has the broad perspective of relating chemical construction of medications and other compounds to the point of being able to change the molecules if the trials fail. This kind of innovation is excellent for patient safety and the doctors’ practices as well.
No appropriate medication treatments should be introduced to public care until all risk factors and dosage requirements are determined through medical testing and clinical pharmacology practices. The whole, integrated process takes patient needs into account, keeping close track of side effects while observing the percentage of patients who drop out due to side effects. You see, the rate at which the drugs are acceptable for patients to use consistently is an important matter, considering that most often patient compliance is a major factor in treatment success. When the proper statistics are gathered with many tiers of observation and care, safer medications can be rapidly developed.