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Introduction - Uppsala Monitoring Centre

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adverse effects more willingly. Now we have effective drugs most of our illnesses<br />

can be cured and we live to have more side effects from the next treatment for the<br />

next illness, but one can see from the life expectancy figures that for our ancestors<br />

their first illness was often their last, as most medicines were to relieve symptoms<br />

rather than cure illnesses. It is apparent that from the earliest times writers have<br />

experimented upon themselves and since they almost certainly did not have the<br />

ailment for which the drug was appropriate the assessment of any reaction would<br />

not have been confused by alternative diagnoses. However, since they were only<br />

experimenting upon themselves only the most common ADR would have been<br />

discovered by this means.<br />

Terminology: the meaning of words changes with passage of time, semantic<br />

shift, and many new specific terms have appeared. There was no standardization of<br />

language, such as MEDRA 180 or its equivalent, so foreign languages need to be<br />

translated and their everyday language interpreted.<br />

5. Publication<br />

1) Prior to 1750 the literature was confined to generalisations befitting their<br />

educational purpose and it was only when medical journals appeared that<br />

individual case histories were published frequently.<br />

2) The herbals, dispensatories and pharmacopoeias covered such a large number<br />

of medicines that it would not have been feasible to mention anything but the<br />

most serious adverse effects.<br />

3) The early authors would not have treated enough patients to pick up a sufficient<br />

number of rare ADRs to have made a generalisation.<br />

4) The steady increase in the number of medical journals published meant that there<br />

was a greater opportunity to be published.<br />

The ever increasing availability of ever increasing numbers of powerful drugs to<br />

an increasingly rich and sophisticated and ever increasing population of patients has<br />

produced and will continue to produce an exponentially increasing number and<br />

variety of ADRs. The number of reported serious adverse events from drug<br />

treatment more than doubled in the United States from 1998 to 2005, rising from<br />

34,966 to 89,842 and the number of deaths relating to drugs nearly tripled from<br />

5,519 to 15,107 (Moore, 2007).<br />

Conclusion<br />

To cover drug safety worldwide across 7,000 years is an impossible task. My<br />

attempt has been restricted by my limited knowledge of foreign languages, the<br />

relative inaccessibility of the data, and time. The means of communication over this<br />

period changed radically from oral to written, written to printed and then from printed<br />

to electronic. From a trickle to a flood; from oracle stones and cuneiform tablets to<br />

Google. The information has varied from warnings of possible death or ‘Poison’ to

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