Pharmacodynamic Phase Flashcards

1
Q

PHARMACODYNAMIC PHASE

A

Study of drug concentration and its effects on the body

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2
Q

Drug response can cause?

A

a primary or secondary physiologic
effect, or both.

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3
Q

Dose Response

A

Relationship between the minimal versus the maximal amount of drug dose needed to produce desired drug response

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4
Q

Maximal Efficacy

A

Maximum drug effect

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5
Q

Onset

A

Time it takes to reach minimum effective concentration after a drug is administered.
Example: start of lowering temperature after fever

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6
Q

Peak

A

Drug reaches the highest blood or plasma concentration
Example: Totally healed

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7
Q

Fastest drug to reach the peak are those given in?

A

IV: 3-10minutes
Oral route: 1-3 hours

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8
Q

Duration

A

Length of time drug has a pharmacologic effect.

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9
Q

Agonists

A

Produce a response
Example: Epinephrine

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10
Q

Antagonist

A

Block a response.
Example: Drug - Cimetidine, Receptor - Histamine

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11
Q

Nonspecific Drug Effects

A

Drugs that affect various body sites
○ Eyes, heart, lungs, GI tract

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12
Q

Nonselective Drug Effects

A

drugs that affect various receptors
○ Alpha 1, Beta 1, Beta 2

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13
Q

CATEGORIES OF DRUG ACTION

A
  1. Stimulation or depression (Nervous System)
  2. Replacement (Taking insulin for Diabetes)
  3. Inhibition, Antimicrobial, Cytotoxic, or Killing of Organisms (Antibacterial, Antifungals)
  4. Irritation (Constipation: can irritate the lining of GI tract to
    perform peristalsis)
  5. Modification of Immune Status (Anti-inflammatory drugs)
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14
Q

Therapeutic Index

A

Estimates margin of safety of a drug
through the use of a ratio that measures the effective dose
and the lethal dose

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15
Q

Drug with Low TI

A

has a narrow margin of safety (hindi ganun ka-safe, needs to be monitored for toxic effects even if tama ang pagadminister).

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16
Q

Drug with High TI

A

has a wide MOS (Margin Of Safety) (very safe).

17
Q

Therapeutic Range

A

Should be between the minimum effective concentration in the plasma for obtaining desired drug action and the maximum toxic concentration.

18
Q

Peak Drug Level

A

Highest plasma concentration of a drug (at a peak level) at a specific time which indicate rate of absorption.

19
Q

Through Drug Level

A

Lowest plasma concentration (taken immediately before the next dose; for low TI) of a drug, which measures the rate at which a drug is eliminated.

20
Q

if a drug’s peak level is high, if a drug’s through level
is high, it means?

A

toxicity can occur

21
Q

LOADING DOSE

A

When immediate drug response is desired, a large initial
dose is given to achieve a rapid minimum effective
concentration in plasma.
Example: Digoxin for CHF, para umepekto agad in improving heart contraction and lessen congestion. Usually has a loading dose.

22
Q

All Loading Dose are?

A

one-time dose, then sinusundan lang ng maintenance dose (which is less dosage).

23
Q

Side Effects

A

Desirable and undesirable
Example: Benadryl (side effect is drowsiness)
■ Taking a certain drug in the morning while taking an exam, and got drowsy (undesirable)
■ Taking a certain drug in the evening to have a good sleep (desirable)

24
Q

Adverse Reactions

A

undesirable (allergic reactions, superinfection, organ toxicity)

25
Q

Toxic Effects

A

dangerous and may be considered lethal.
○ Drugs with low TI; can cause neurotoxicity, autotoxicity, hepatotoxicity, and nephrotoxicity

26
Q

PHARMACOGENETICS

A

Effect of a drug action that varies from a predicted drug
response because of genetic factors or hereditary influence. (not effective for other race)

27
Q

Tolerance

A

Decreased responsiveness over the course of therapy.
Ex: Drug tolerance for narcotics can result in decrease pain relief. To avoid tolerance, drugs must be finished.

28
Q

Tachyphylaxis

A

Rapid decrease in response to the drug. Acute tolerance.

29
Q

PLACEBO EFFECT

A

Psychologic benefit from a compounds that may not have
the chemical structure of a drug effect
○ Usually done in clinical drug studies