Pharmacotherapy Flashcards

1
Q

What is Pharmacokinetics?

A

“what the drug does to the body”, describes a drug’s pathway into, through and out of the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the four phases of pharmacokinetics?

A

Absorption, Distribution, Metabolism and Excretion (ADME)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What could Pharmacokinetics help with?

A

Define onset, duration and intensity of a drugs effect (which could be impacted by patient related factors and drug properties)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What factors influence drug response?

A

-physiologic: age, sex, weight
-pathophysiologic: kidney and liver function
-Genetic variability: lack of certain enzymes
-drug interaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the three ways for a drug to cross a cell membrane?

A
  • direct penetration of cell membrane
    -channel and pores
    -transport systems
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Factors affecting drug absorption:

A

-rate of dissolution
- surface area
- blood flow
- lipid solubility
- pH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the bioavailability of IV drugs?

A

100%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is bioavailbility?

A

its amount of drug absorbed / drug dose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is bioavailability affected by?

A

Gastric Emptying time, the pH of the Stomach, The speed of the drugs moves through the GI tract

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is Bioequivalence?

A

2 different drugs products or dosage forms of the same drug produce the same concentration vs. time curves (important for generic products)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the First Pass Effect?

A

The First Pass Effect is when drugs taken orally travel from the GI tract to the liver through the hepatic portal circulation. In the liver, they can be metabolized or inactivated before entering the bloodstream, which can reduce their therapeutic effects. To avoid this, drugs can be administered through other routes like parenteral, sublingual, or transdermal. An example is nitroglycerin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the characteristics, advantages, and disadvantages of the Intravenous (IV) route of drug administration?

A

Characteristics:

No barriers to absorption, leading to instant and complete drug delivery.

Advantages:

Rapid onset of action.
Precise control over drug administration.
Suitable for dissolving drugs in large fluid volumes.
Allows safe administration of irritant drugs through high-flow veins.
Disadvantages:

High cost and inconvenience.
Safety issues associated with IV administration.
Irreversibility once administered.
Risk of fluid overload.
Potential for infection at the injection site.
Possibility of embolism when not properly administered.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are the characteristics, advantages, and disadvantages of Intramuscular (IM) and Subcutaneous (SC) routes of drug administration?

A

Characteristics:

No significant barriers to absorption as drugs can pass freely through the capillary wall.
Absorption pattern depends on drug solubility in water and blood flow.
Advantages:

Suitable for poorly soluble drugs.
Can be used for depot preparations, allowing slow, sustained release of medication.
Disadvantages:

Discomfort and potential pain associated with injection.
Inconvenience compared to oral administration.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the characteristics, of the oral route of drug administration, including different dosage forms?

A

Characteristics:

Barriers to absorption: epithelial cells lining GI tract, capillary wall (most drugs pass freely).
Absorption pattern influenced by: drug solubility and stability, gastric and intestinal pH, gastric emptying, presence of food, co-administration of other drugs, and dosage form (e.g., enteric coating).

Dosage Forms:

Liquids: suspensions, emulsions, elixirs, solutions.
Capsules: hard (can be opened, immediate or controlled release), soft (generally cannot be opened).
Tablets/Caplets: various types (immediate release, enteric coated, extended release, etc.), caution with extended release forms (cannot be crushed, if scored can be halved). Check drug monographs for specific instructions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the advantages, and disadvantages of the oral route?

A

Advantages:

Easy and convenient administration.
Available in many dosage forms.
Inexpensive compared to other routes.
Generally considered safe.
Disadvantages:

Variability in absorption.
Potential inactivation of the drug during digestion.
Specific patient requirements (e.g., ability to swallow).
Possible local irritation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How do you calculate volume distribution?

A

Amount of drug in body/ plasma concentration— it is the movement of drugs through the body

17
Q

What factors affect the pharmacokinetics?

A
  • Blood flow to tissues
    -exiting the vasculature
  • blood brain barrier (BBB)
  • placental drug transfer
  • protein binding
  • ability of drug to pass through cells (relies on lipid solubility,
    transport systems, etc.)
18
Q

Which of the following will enter tissues readily and decrease concentration in the blood?

a) high protein bound drugs
b) Low protein Bound Drugs

A

Low Protein Bound Drugs

19
Q

Most drugs pass through the ____ and metabolized by cytochrome ______ enzymes or ______ enzymes.

A

(1) liver (2) P450 (3) CYP

20
Q

What do Enzyme Inducers do?

A

Decrease level of drug in the body

21
Q

What do Enzyme Inhibitor do?

A

Increase level of drug in body

22
Q

How does excretion happen?

A

VIA Urine, Bile, Sweat, Saliva, Expired air or breast milk

23
Q

3 processes of renal drug excretion

A

Glomerular Filtration
Passive Tubular Secretion
Active Tubular Secretion

(GPA)

24
Q

Factors affecting renal drug excretion

A

1) PH Dependent ionization (like absorbs like)
2) Competition for active tubular transport
3) Age (newborn have limited capacity to excrete drugs)

25
Q

What is Half life and what does it effect?

A

Half life= time required for amount of drug in body to decrease by 50%
It impacts dose interval

26
Q

Loading Dose

A

Large Initial dose to reach the therapeutic range more quickly

27
Q

Maintenance Dose

A

Smaller dose given to remain in the plateau stage once its reached

28
Q

Pharmacodynamics

A

The study of what drugs do the body and how they do it

29
Q

Dose response relationship

A
30
Q

Affinity

A

The strength of attraction between a drug and its receptor

31
Q

Intrinsic Activity

A

The ability of a drug to activate a receptor following binding

32
Q

Agonists

A

Mimic the body’s own regulatory molecules

33
Q

Antagonists

A

Block the actions of endogenous regulators

34
Q

Drug Interaction

A

An interaction where the efficacy or toxicity of one or more of the drugs is altered

35
Q

Types of drug interactions

A

1) drug-drug
2) drug-food
3) drug-herb

36
Q

Pharmacokinetics changes ____ levels

A

drug levels

37
Q

Pharmacodynamics enhances the ___ of drugs

A

effect

38
Q
A