MimiHapa MEDICINE as HOME OF MEDICINE Share with medical student of pharmacy known as pharmaceutical science course (PST) a collection of past paper questions of pharmacy for subject of Monitoring and Evaluation of Medicine Use Questions For Pst Nta Level 6, These are collections of question from the previously past paper, As Pharmacy Questions Time. So below are those question of Monitoring and Evaluation of Medicine Use can pass through it and try to solve those question and be completely on it (module)
1. What is a pharmacovigillance method?
2. What is spontaneous reporting?
3. What is targeted reporting?
4. What are tools used in monitoring and evaluation of medicine use?
5. What are components of level one questionnaire?
6. What are the common medicine use indicators?
7. What is the application of the medicine use indicators?
8. What are the three level indicators for pharmaceutical assessment?
9. What the components of level 1 and level 2 indicators?
10. How can we measure improved access, quality and rational use of medicine?
11. Mention factors hindering monitoring and evaluation of medicine use
12. To each mention factor above mention measures to be taken to overcome them.
13. What are the components of WHO operational package for assessing and monitoring country pharmaceutical situation?
14. What are pharmaceutical indicators for monitoring and assessment?
15. What are the aims of monitoring and assessment of pharmaceuticals?
16. Who can use the results of monitoring and assessment of pharmaceuticals?
17. What is monitoring?
18. What is evaluation?
19. What is the difference between monitoring and evaluation?
20. Why is it important to conduct monitoring and evaluation?
21. What is the necessary information required in documentation of ADRs?
22. Mention types of ADRs reporting forms?
23. Who help in gathering data in ADRs occurrences?
24. What is ADRs?
25. Classify ADRs?
26. What are predisposing factors for ADRs?
27. What are the ways of reporting Pharmacovigillance data?
28. What are general information should Pharmacovigillance reporting forms contain?
29. What are the tools used for Monitoring Medicines safety?
30. What are characteristics of good documentation practices in pharmacovigilance?
31. How are pharmacovigilance Data and records managed?
32. What are the tools used for Monitoring Medicines safety?
33. What are characteristics of good documentation practices in pharmacovigillance?
34. How are pharmacovigillance Data and records managed?
35. What are the tools used for Monitoring Medicines safety?
36. What are characteristics of good documentation practices in pharmacovigillance?
37. How are pharmacovigillance Data and records managed?
38. What is a pharmacovigillance method?
39. What is spontaneous reporting?
40. What is targeted reporting?
41. What are counterfeit medicines?
42. What are substandard medicines?
43. What is the effect of substandard and counterfeit
44. medicines to the public health?
45. What to report in ADRs?
46. When to report ADRS?
47. What information is required in ADRs case report?
48. What are the ways to identify counterfeit and substandard medicines?
49. What is mini lab test kit?
50. What are the uses of TLC?
51. What are the methods to control substandard and counterfeit medicines?
52. What measures can be taken to control spread of substandard and counterfeit medicines in Tanzania?
53. What are factors contributing to existences of counterfeit and substandard medicines?
54. Mention points of entry of substandard and counterfeit medicines in Tanzania?
55. What are the loopholes that contribute to spread of substandard and counterfeit medicines in health system?
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