The problems relating to the use of medicines are manifold. They may differ
in pharmacological, pathological, epidemiological and legal respects, and
may have different consequences, for example, as regards scientific study,
regulation or rational use. Pharmacovigilance is concerned with all such pr
oblems: adverse effects and interactions as well as problems relating to in
effectiveness, inappropriate use, counterfeiting, dependence or poisoning.
Practically all medicine-related problems can be classified in one basic sy
stem, taking into account their characteristics and distinctions. This syst
em distinguishes between appropriate and inappropriate drug use, dose-relat
ed problems, and types A ('drug actions'), B ('patient reactions') and C ('
statistical') adverse effects. This classification may serve as an educatio
nal tool and may be useful in when choosing a study method and for the desi
gn of effective strategies in pharmacovigilance.