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Clinical trials are usually done on young, healthy male volunteers. Obviously, in therapeutic use drugs are taken by many different sectors of the general population least likely to be young, healthy men. Drug trials therefore continue after a drug is on the market through monitoring by the MHRA of the first patients using new drugs and through the yellow card scheme of reporting adverse reactions thereafter. It is possible to predict, and to some extent avoid, likely adverse effects in particular populations using knowledge of factors that affect the four processes above in different patient groups.

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