Back to marketplace

Introduction To Pharmacology - Tutorial 4

No description yet. This curated deck is ready for daily study.

Total cards: 8•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (8)

#1
Front (Question)

Define the three different drug names

Back (Answer)

• Chemical name: describes the chemical composition, e.g. N-acetyl-p-aminophenol • Generic name: the official name listed in publications and used for prescribing. E.g paracetamol • Trade (brand name): marketed name, E.g. Panadol

#2
Front (Question)

Define the term pharmacodynamics

Back (Answer)

The effect of the drug on the body

#3
Front (Question)

Define the terms agonist & antagonist

Back (Answer)

• Agonist - binds to and activates receptor • Antagonist - binds to and deactivates receptor

#4
Front (Question)

Define the term pharmacokinetics

Back (Answer)

How the body affects a specific drug after administration

#5
Front (Question)

Name and describe the four pharmacokinetic processes in correct sequence

Back (Answer)

• Absorption - refers to the passage of medications from the site of administration into the blood. • Distribution - refers to the movement of the drug from the blood to the body’s tissues. • Metabolism - is the process of chemical modification of the drug • Excretion - is the removal of the drug from the body

#6
Front (Question)

State three factors that would influence each of the four pharmacokinetic processes

Back (Answer)

• Absorption: • Route of delivery • Body surface area • Blood flow to the area of absorption • Distribution: • Tissue binding • Cardiac function • Capillary permeability • Metabolism: • Genetics • Age • Disease states • Environmental factors (e.g diet) • Excretion: • Sweat • Bile • Breast milk

#7
Front (Question)

State five ways that drugs can be excreted

Back (Answer)

• Sweat • Bile • Breast milk • Faeces • Expired Air

#8
Front (Question)

Explain hepatic first pass effect & drug bioavailability

Back (Answer)

• Hepatic first pass effect - orally admistered drugs travel first through the portal system and liver before entering the systemic circulation - a variable amount of drug may be extracted before entering the systemic circulation Drug bioavailability - The proportion of the administered dose that reaches the systemic circulation intact - drugs delivered intravenously have 100% bioavailability