Pharmacology and Pathology 1, 7.5 credits
Farmakologi och sjukdomslära 1, 7.5 hp- Course code
- 2DS001
- Course name
- Pharmacology and Pathology 1
- Credits
- 7.5 credits
- Form of Education
- Higher Education, study regulation 2007
- Main field of study
- Not applicable
- Level
- AV - Second cycle
- Grading scale
- Pass with distinction, Pass, Fail
- Department
- Department of Laboratory Medicine
- Decided by
- Programnämnden för sjuksköterskeutbildning och specialistutbildningar för sjuksköterskor
- Decision date
- 2007-06-05
- Revised by
- Education committee NVS
- Last revision
- 2017-03-13
- Course syllabus valid from
- Autumn 2008
Specific entry requirements
Qualification as a nurse certified by the National Board of Health and Welfare
Objectives
On completion of the course, the student should be able to understand and apply general pharmacological principles and the legislation regulating the use of drugs.
This course should, together with Pharmacology and pathology part 2, lead to qualification requirements for a specialist nurse to apply for prescription right of drugs for patients according to the Swedish National Board of Health and Welfare's Regulation (2001:16) of qualification requirements in the prescription of drugs
The course is divided in two parts.
Part 1: General pharmacology, 4.5 higher education credits
On completion of the part, the student should be able to understand and apply pharmacodynamic and pharmacokinetic principles related to:
- origin of effects and side effects of drugs
- pharmaceutical form and administration methods
- age, sex and genetic variability, and environmental factors
- pregnancy and breast feeding
- relation between dose, concentration and the effect of drugs
- origin of adverse drug reactions, interactions and release problems
Part 2: Drug-related legal framework, 3 higher education credits
A student should, on completion of the part, be able to analyse and apply:
- Pharmacy law (1992:859) and Pharmacy regulation (1992:1752), and related regulations and general guidelines
- LVFSF 2001:12 The Medical Products Agency's regulations of security assurance of drugs
- The regulations and general guidelines of the Swedish National Board of Health and Welfare (SOSFS 2000:1) of drug management in the health care
- Regulation (SOFS 2001:16) of qualification requirements for nurses in the prescription of drugs
- The regulations of the Medical Products Agency (LVFS 1997:10) of the prescription and distribution of drug etc
Student should also be able to:
- describe and understand principles of drug evaluation
Content
Part 1: General pharmacology, 4.5 higher education credits.
The main contents of the part focus on pharmacodynamic respective pharmacokinetic principles.
Part 2: Drug-related legal framework, 3 higher education credits.
The main contents of the part consist of laws and regulations concerning drugs and drug management, including the nurse's drug prescription.
General pharmacology, 4.5 hp
Drugrelated legal framework, 3.0 hp
Teaching methods
The course contains different working methods such as lectures, seminars, group discussions, assignments and independent knowledge acquisition and evaluation of the retrieved information.
When the course is given as Distance education
The distance education is IT-based and is characterised by independent and collaborative learning. Different working methods such as individual study assignments, work in groups, virtual discussions and seminars and lectures are used. The number of physical meetings is limited to at most 2 days/7.5 credit points
Examination
Part 1: All the outcomes are examined through a written examination.
Student without approved results after three completed examinations may be offered to take the course once more. However, there are at most six examination opportunities for each course. Examination times are announced at the beginning of the course. In case of failure of a written group examination, written individual examinations are required as above.
Part 2: - Pharmacy law and Drug legislation and related regulations and general guidelines are examined by an individual written assignment.
- Other outcomes are examined at seminars.
In case of absence from seminars, a written complementary assignment should be submitted for approval according to the course director's instructions.
For a Pass with distinction in the course, the grade Pass with distinction in the part General pharmacology 4.5 credits, is required.
Transitional provisions
The course has been cancelled.
Other directives
Course evaluation takes place in accordance with the guidelines established by the Board of Education.
Literature and other teaching aids
Lund : Studentlitteratur, 2005 - 140 s. ISBN:91-44-03540-3 LIBRIS-ID:9889402 Library search
senaste uppl. : Läkemedelsinformation AB, URL: www.fass.se
Stockholm : Liber, 2007 - 727 s. ISBN:978-91-47-08420-3 LIBRIS-ID:10324013 Library search
Stockholm : Apoteket AB, 2007 - 1260 s. ISBN:91-85574-57-0 LIBRIS-ID:10399282 Library search
3., [rev.] uppl. : Stockholm : Apotekarsocieteten, 2005 - 86 s. ISBN:91-974318-8-5 (korr.) z 97-43-188-5 LIBRIS-ID:10004488 Library search
Stockholm : Natur och kultur, 2001 - 273 s. ISBN:91-27-07715-2 (inb.) LIBRIS-ID:8240046 Library search
5., [rev. och uppdaterade] uppl. : Lund : Studentlitteratur, 2004 - 379 s. ISBN:91-44-02782-6 LIBRIS-ID:9208589 Library search
Stockholm : Socialstyrelsen, 2004 - 20 s. ISBN:91-7201-897-6 LIBRIS-ID:9692096 URL: http://www.socialstyrelsen.se/NR/rdonlyres/1B771FA3-F290-4CBE-B7A6-705DB19642B7/2671/20041015.pdf Library search