Abstract:Background
Pregnant women are usually excluded from clinical drug trials. However, many women take medicines while they are fertile. Because of this, the pharmacy department agreed with the Department of Obstetrics and Gynaecology (DOG) to write drug teratogenicity reports (TDR) for pregnant women (or women who desired a child).
Purpose
To evaluate drug teratogenicity and write reports as requested by the DOG. Furthermore, to assess the suitability of prescriptions in the light of recommendations drawn up by… Show more
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