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Course, academic year 2025/2026
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OS - Clinical Pharmacology - DVA1028
Title: OS - Clinical Pharmacology
Guaranteed by: Department of Medical Chemistry and Clinical Biochemistry (13-352)
Faculty: Second Faculty of Medicine
Actual: from 2023
Semester: summer
Points: 3
E-Credits: 3
Examination process: summer s.:
Hours per week, examination: summer s.:0/20, C [HS]
Capacity: unknown / unknown (10)
Min. number of students: 5
4EU+: no
Virtual mobility / capacity: no
Key competences:  
State of the course: taught
Language: English
Teaching methods: full-time
Level:  
Note: course can be enrolled in outside the study plan
enabled for web enrollment
Guarantor: prof. MUDr. Richard Průša, CSc.
MUDr. Hundie Tesfaye, Ph.D.
Annotation - Czech
The Optional Subject is mainly recommended to 5th year and above students of General Medicine Organized by: Department of Medical Chemistry and Clinical Biochemistry, Division of Clinical Pharmacology. All interested may contact: MUDr. Hundie Tesfaye, Ph.D. on ext. Tel. 5656, Motol Hospital Capacity: max. 10 students/group The Optional Subject is planned to take place from 20. 4. - 24. 4. 2026 for international students group usually starting at 14:00 i.e., 3-4 hours for five consecutive working days. Location: Second Floor, G (Pediatric part of the hospital building). Unless announced to be elsewhere.
Last update: Hrůšová Michaela, Bc., DiS. (15.09.2025)
Course completion requirements

Lectures on days 2 -5 will be followed by workshops aiming interactive discussion and case

supported learning and decision-making.

Terms and conditions to get course attendance credits:

Attendance of minimum 4 out of 5 days or 3 out of 5 days provided that an attendee must perform

pharmacological analysis of 4 model clinical cases including appropriate resolution and

recommendations.

N.B.: International students, who attended the course as complementary to Erasmus programme,

must take examination composed of triple of questions only in case they request classified

grading/marks.

Last update: Greňo Václav (11.12.2025)
Literature - Czech
In case of request /need reference books will be indisposition for the course attendees.

The following reference books will be indisposition for the course attendees:

1. Chatu: The Hands-on Guide to Clinical Pharmacology ISBN-13: 978-1405191951

2. Ebadi: Desk Reference of Clinical Pharmacology ISBN-13: 978-1420047431

3. Wecker, Lynn : Brody's human pharmacology :molecular to clinical.

Philadelphia, Mosby Elsevier, 5th ed. ISBN 978-0-323-05374-7

4. Hyacinth Martin: Clinical Decision Making: Case Studies in Pharmacology ISBN-13: 978-1401835217

5. A textbook of clinical pharmacology and therapeutics / London : Hodder

Arnold, 2008. 5th ed. ISBN 978-0340900468

6. Clinical pharmacology / Bennett, P. N. Edinburgh ; New York : Churchill

Livingstone, 10th ed. ISBN 9780443102448

7. Applying medication math skills : a dimensional analysis approach / Karen Clement-O'Brien, Gary M. Lawler.. Albany : Delmar Publishers, c1999.

8. Applied therapeutics : the clinical use of drugs / edited by Mary Anne Koda-Kimble ... [et al.].. Philadelphia : Wolters Kluwer/Lippincott Williams & Wilkins, c2009.

Last update: Palowska Stanislava (14.09.2021)
Requirements to the exam

The formal examination is not applicable after this course.

Last update: Palowska Stanislava (14.09.2021)
Syllabus
Organized by: Department of Medical Chemistry and Clinical Biochemistry,
Division of Clinical Pharmacology.
All interested may contact Mudra. Hundie Tesfaye, Ph.D. on ext. Tel. 5656, Motol Hospital

Capacity: max. 10 students/group

The Optional Subject is scheduled to take place from 20. 4. - 24. 4. 2026 usually starting at 14:00 and lasting 3-4 hours for five consecutive working days.

Location: Second Floor, G (Pediatric part of the hospital building), unless announced to be elsewhere.

Context:
During the study of preclinical compulsory courses, the medical student is hardly engaged in patient management or confronted with the real clinical problem. Pharmacology is one of the basic subjects included in mandatory preclinical subjects, where the student mainly works hard to overcome anatomy of drugs and classes.

Therefore, the course offered now is aiming to help the shortly graduating future physicians how to practice rational pharmacotherapy. The course is limited to few students to work in small group after consecutive lectures. After attending the course supported by interactive discussion and case problem solving, the student is expected to have better knowledge of modern aspects of pharmacokinetics and its clinical importance, challenges associated to clinical trials and good clinical practice, problem of generics versus patented drugs, drugs prescription in special population, importance of therapeutic drug monitoring and rational pharmacotherapy.

The overall scope of the course is to emphasize the need of individual approach to help achieving quality care for patients complying with the evidence-based medicine.

Day 1.
(20.4.2026)

Core lectures:

  • Introduction to Clinical Pharmacology
  • Good Clinical practice
  • Phases of Clinical trials in human subjects I-IV and ethical challenges
  • Pharmaceutical aspects of drugs and clinical importance
  • Adverse drug reactions, role of pharmacovigilance

Day 2.
(21.4.2026)

Lecture + Work-shop

  • Standard operation procedures during drug prescription/good prescribing practice.

Day 3.
(22.4.2026)

Lecture + Work-shop

  • Special population PK/PD and clinical importance

Day 4.
(23.4.2026)

Lecture + Work-shop

  • Drug-drug interaction risk, PK/PD and toxicological significances

Day 5.
(24.4.2026)

Lecture + Work-shop

  • Importance and methods of therapeutic drug concentration monitoring in biological specimen

Lectures on days 2-5 will be followed by workshops aiming interactive discussion and case supported learning and decision-making.

Last update: Greňo Václav (11.12.2025)
Schedule semestral
Educational week Date From - To Education type Theme Teacher Files Note
2820.04.202614:00 - 18:00lecture+seminarIntroduction to Clinical Pharmacology Good Clinical practice Phases of Clinical trials in human subjects I-IV and ethical challenges Pharmaceutical aspects of drugs and clinical importance Adverse drug reactions, role of pharmacovigilance MUDr. Hundie Tesfaye, Ph.D. 
21.04.202614:00 - 18:00lecture+seminarStandard operation procedures during drug prescription/good prescribing practice. MUDr. Hundie Tesfaye, Ph.D. 
22.04.202614:00 - 18:00lecture+seminarSpecial population PK/PD and clinical importanceMUDr. Hundie Tesfaye, Ph.D. 
23.04.202614:00 - 18:00lecture+seminarDrug-drug interaction risk, PK/PD and toxicological significancesMUDr. Hundie Tesfaye, Ph.D. 
24.04.202614:00 - 18:00lecture+seminarImportance and methods of therapeutic drug concentration monitoring in biological specimen MUDr. Hundie Tesfaye, Ph.D. 
 
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