1. Define
(a) Professional misconduct
(b) Breaches
(c) Pharmacy practice
2. A pharmaceutical personnel must
have regard for human life what are the obligations of pharmaceutical personnel on.
(a)
Induction
or inhibition of gestation.
…………………………………………………………………………………………………………………………………………………..
(b)Growth, development and performance
enhancer
…………………………………………………………………………………………………………………………………………………….
(c)
Termination
of life:
…………………………………………………………………………………………………………………………………………………...
3. A pharmaceutical personnel must ensure access
to essential medicine. Mention five (5) obligation
..................................................................................................................................................
4. A pharmaceutical personnel should
ensure availability of safe, efficacious and quality medicines. Mention five (a) obligations of the pharmaceutical personnel.
..................................................................................................................................................
5 (a) Mention code of ethics number
five
……………………………………………………………………………………………………….
(b) Mention (four) 4 obligation of pharmaceutical personnel on code of
ethics number 9.
…………………………………………………………………………………………………………………………..
6. Mention medicines and medical
supplies provided at a dispensary level.
………………………………………………………………………………………………….…………………………
7. Section 36 of the pharmacy act no. 1 of 2011 is about application for
Permits. Describe it
………………………………………………………………………………………………………………………………………………………
8. (a) Define
unfit medicine and cosmetic products
………………………………………………………………………………………………………………………………………………………
(b)Describe the procedures for handling of unfit medicine and cosmetics
products at facility level
……………………………………………………………………………………………………………………………………………………………..
9. Mention Minimum important information in the
Register book:
……………………………………………………………………………………………………………………………….
10. Mention Minimum important information in
Application Form for Disposal of unfit and cosmetics products.
………………………………………………………………………………………………………………………………………………………..
11. Draw a
format of Annex 1
………………………………………………………………………………………………………………………………..
12. What are the names of the following forms?
Annex
I ………………………………………………………………………………………
Annex II ………………………………………………………………………………………
Annex III
……………………………………………………………………………………..
Annex IV ………………………………………………………………………………………
13. What is inspection checklist forms?
……………………………………………………………………………………………
14. Define sorting of unfit medicines and cosmetic products.
…………………………………………………………………………………………………………………………………
15. Complete the table bellow
|
S/N |
Categories |
Disposal
methods |
|
1. |
Solids, semi-solids and Powders |
|
|
2. |
Liquids |
|
|
3. |
Antineoplastics |
|
|
4. |
Treated waste and landfill, high temperature incineration |
|
|
5. |
Landfill without waste inertization |
|
|
6. |
Disinfectants |
|
|
7. |
PVC plastics, glass (ampoules, bottles and vials) |
|
|
8. |
Recycle, burn, landfill |
16. Describe the procedures for sorting of unfit
medicine and cosmetics products
…………………………………………………………………………………………………………………………………………………………
17. Verification
process shall involve the following stages. Mention
……………………………………………………………………………………………………………………………………………………
18. Describe Verification
Exercise of Unfit Medicines and Cosmetic Products.
…………………………………………………………………………………………………………………………………………………….
19. Create a Model of Verification Form of
unfit medicine and cosmetics products
……………………………………………………………………………………………………………………………………………………
20. Where do members/Participants of
destruction of unfit medicine and cosmetics products are chosen from. Mention?
…………………………………………………………………………………………………………………………………….
21.
Mention members/Participants involved in destruction of unfit medicine and
cosmetics products
…………………………………………………………………………………………………………………………………………………….
22.
Describe the procedures for destruction of unfit medicine and cosmetics
products.
…………………………………………………………………………………………………………………………………………..
23. What
is the Certificate of Destruction of Unfit Medicines and Cosmetic Products?
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