TAILIEUCHUNG - CLINICAL PHARMACOLOGY 2003 (PART 6)

We must be daring and search after Truth; even if we do not succeed in finding her, we shall at least come closer than we are at present (Galen AD 130-200) SYNOPSIS (CONTINUED) Surveillance studies and the reporting of spontaneous adverse reactions respectively determine the clinical profile of the drug and detect rare adverse events. Further trials to compare new medicines with existing medicines are also form the basis of cost-effectiveness comparisons. Topics include: • Experimental therapeutics • Ethics of research • Rational introduction of a new drug • Need for statistics • Types of trial: design, size •. | SECTION I Evaluation of drugs in man We must be daring and search after Truth even if we do not succeed in finding her we shall at least come closer than we are at present Galen AD 130-200 SYNOPSIS This chapter is about evidence-based drug therapy. New drugs are gradually introduced by clinical pharmacological studies in rising numbers of healthy and or patient volunteers until enough information has been gained to justify formal therapeutic studies. Each of these is usually a randomised controlled trial where a precisely framed question is posed and answered by treating equivalent groups of patients in different ways. The key to the ethics of such studies is informed consent from patients efficient scientific design and review by an independent research ethics key interpretative factors in the analysis of trial results are calculations of confidence intervals and statistical potential clinical significance needs to be considered within the confines of controlled clinical is best expressed by stating not only the percentage differences but also the absolute difference or its reciprocal the number of patients who have to be treated to obtain one desired outcome might include both efficacy and safety. SYNOPSIS CONTINUED Surveillance studies and the reporting of spontaneous adverse reactions respectively determine the clinical profile of the drug and detect rare adverse events. Further trials to compare new medicines with existing medicines are also form the basis of cost-effectiveness comparisons. Topics include Experimental therapeutics Ethics of research Rational introduction of a new drug Need for statistics Types of trial design size Meta-analysis Pharmacoepidemiology Experimental therapeutics As the number of potential medicines produced increases the problem of whom to test them on grows. There are two main groups healthy volunteers and volunteer patients plus rarely nonvolunteer patients . .

TỪ KHÓA LIÊN QUAN
TAILIEUCHUNG - Chia sẻ tài liệu không giới hạn
Địa chỉ : 444 Hoang Hoa Tham, Hanoi, Viet Nam
Website : tailieuchung.com
Email : tailieuchung20@gmail.com
Tailieuchung.com là thư viện tài liệu trực tuyến, nơi chia sẽ trao đổi hàng triệu tài liệu như luận văn đồ án, sách, giáo trình, đề thi.
Chúng tôi không chịu trách nhiệm liên quan đến các vấn đề bản quyền nội dung tài liệu được thành viên tự nguyện đăng tải lên, nếu phát hiện thấy tài liệu xấu hoặc tài liệu có bản quyền xin hãy email cho chúng tôi.
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.