how them drugs work and adrs - Sheet1 Flashcards

1
Q

What is maximal efficacy?

A

The largest effect a drug can produce.

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

Why is maximal efficacy important in patient care?

A

It ensures the intensity of the medication aligns with the patient’s needs.

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

What is relative potency?

A

The amount of a drug needed to produce an effect.

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

What is a receptor in receptor theory?

A

A cellular molecule to which a drug binds to produce its effects.

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

How do drugs interact with receptors?

A

They mimic or block regulatory molecules, altering physiological activity.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the “lock and key” model in drug-receptor binding?

A

Drugs fit receptors like a key fits a lock, either activating or blocking the receptor.

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

What are agonists?

A

Drugs that activate receptors and mimic the body’s regulatory molecules.

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

What characteristics do agonists have?

A

Affinity and high intrinsic activity.

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

What are antagonists?

A

Drugs that block receptors and prevent receptor activation.

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

Do antagonists have intrinsic activity?

A

No, they have affinity but no intrinsic activity.

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

What are partial agonists?

A

Drugs that activate receptors but produce a smaller response than full agonists.

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

How do noncompetitive antagonists work?

A

They bind irreversibly to receptors, reducing the maximal response.

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

Is the impact of noncompetitive antagonists permanent?

A

No, new receptors are synthesized over time.

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

How do competitive antagonists work?

A

They bind reversibly to receptors, with the highest concentration determining receptor occupation.

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

What are the three outcomes of drug interactions?

A

Increased effects, decreased effects, or unique responses.

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

Name four basic mechanisms of drug-drug interactions.

A

Direct chemical/physical interaction, pharmacokinetic interaction, pharmacodynamic interaction, and combined toxicity.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Why are drug interactions significant for drugs with a narrow therapeutic range?

A

Small changes in drug levels can lead to toxicity or therapeutic failure.

18
Q

How can the risk of drug interactions be minimized?

A

Reduce the number of drugs, take thorough histories, adjust dosages/timing, and monitor for toxicity.

19
Q

How does grapefruit juice interact with medications?

A

It can increase the levels of certain drugs in the blood, enhancing effects or toxicity.

20
Q

Name a drug class significantly affected by grapefruit juice.

A

Calcium channel blockers, statins, benzodiazepines, and immunosuppressants.

21
Q

Give an example of a calcium channel blocker affected by grapefruit juice.

A

Felodipine (Plendil) or Nifedipine (Procardia, Adalat).

22
Q

Name a statin that interacts with grapefruit juice.

A

Atorvastatin (Lipitor) or Simvastatin (Zocor).

23
Q

Name a benzodiazepine that interacts with grapefruit juice.

A

Diazepam (Valium) or Midazolam (Versed).

24
Q

What are some neurological medications affected by grapefruit juice?

A

Buspirone (BuSpar), Sertraline (Zoloft), or Carbamazepine (Tegretol).

25
Q

What are adverse drug reactions (ADRs)?

A

Undesirable effects that occur at normal drug doses.

26
Q

Who is at the highest risk for ADRs?

A

The very old, very young, and individuals with severe illness.

27
Q

What is a side effect?

A

An unintended, predictable secondary effect of a drug at normal therapeutic doses, usually not serious.

28
Q

What is toxicity?

A

Harmful effects of a drug caused by excessive dosing or unsafe levels in the body.

29
Q

What organs are commonly affected by toxic drug effects?

A

Liver, kidneys, heart, lungs, inner ear, bone marrow, skeletal muscle, tendons.

30
Q

What are signs of hepatotoxicity?

A

Liver failure, jaundice, dark urine, light stool, nausea/vomiting, RUQ pain, appetite loss.

31
Q

What is an allergic reaction?

A

A hypersensitive immune response to a drug, often involving histamine release.

32
Q

Are severe allergic reactions common?

A

No, very few drugs cause severe allergic reactions.

33
Q

What is an idiosyncratic effect?

A

A rare, unpredictable drug response unique to an individual due to genetic differences.

34
Q

What is a paradoxical effect?

A

A drug effect opposite to what is expected.

35
Q

What is iatrogenic disease?

A

A condition unintentionally caused by medical treatment or drugs.

36
Q

What is physical dependence?

A

The body’s adaptation to a drug, leading to withdrawal symptoms when stopped suddenly.

37
Q

What is a carcinogenic effect?

A

The ability of a drug to cause cancer.

38
Q

What is a teratogenic effect?

A

The ability of a drug to cause developmental abnormalities in a fetus.

39
Q

How can ADRs be prevented?

A

Obtain thorough medical history, assess the patient, avoid med errors, know usual side effects, watch for ADRs, and educate patients/families.

40
Q

What is a Black Box Warning?

A

The strongest safety warning issued by the FDA.

41
Q

What is REMS?

A

Risk Evaluation and Mitigation Strategies to reduce drug-related harm.

42
Q

How are serious ADRs reported in the US?

A

Through organizational policy or MedWatch, a voluntary reporting system.