Kinetics 14.5 - 16 Flashcards

1
Q

Fraction or percentage of the drug removed from the perfusing blood during passage through the organ

A

EXTRACTION RATIO

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2
Q

Measure of the elimination of the drug by that organ

A

EXTRACTION RATIO

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3
Q

EXTRACTION RATIO

T/F: Drugs with high hepatic extraction ratio have large
1st-pass effect

A

True

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4
Q

EXTRACTION RATIO

T/F; One of the highest extraction would actually be your hepatic extraction

A

True

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5
Q

EXTRACTION RATIO

Notice that all the administered drug passes
through the portal circulation and is immediately acted upon by the (liver/Kidney)

A

Liver

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6
Q

EXTRACTION RATIO

T/F: Although there are also some drugs that need to
pass through the liver to be activated but most are
inactivated and are prepared to be excreted

A

True

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7
Q

EXTRACTION RATIO

There is a renal clearance dumping them out into the urine either through the process of _______ or to ________

A

filtration; tubular secretion

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8
Q

Drugs are eliminated unchanged or as metabolites

A

EXCRETION

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9
Q

EXCRETION

(Polar/Non Polar) compounds are more efficiently eliminated

A

Polar

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10
Q

EXCRETION

most important organ

A

Kidneys

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11
Q

When will we take the peak concentration?

For IV, we said around 30 minutes after IV administration
2-3 hours for oral administration

A

When it
is already fully absorbed or distributed

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12
Q

: What happens when the peak concentration is
above the minimum toxic?

For example, at 18 units mg/L meaning its
already a toxic concentration of the plasma
concentration. How will you act and adjust the dose?

A

You lower down the dose

Let’s say you give 10 mg/mL yung
concentration, since your peak is outside
the therapeutic window , you will make it 5
or 8 mg/mL

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13
Q

What happens when your trough concentration would fall below the minimum effective concentration?

A

You increase the dose; If you increase the dose, you will increase the plasma concentration

It’s possible that it won’t breach; however,
since you increased the dose, the rate of
eliminated becomes faster so that at the
end of your dosing interval it will dip down
below the effective concentration. What you need to do is shorten the dosage interval or increase the frequency of
dosing . If that was every 8 hours, you need to give
the next dose at 6 hours, so that it won’t go
down

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13
Q

Drug used for COPD and asthma

A

Theophylline

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14
Q

Is this the reason why yung iniinom na gamot
need i-take every specific hours?

A

Yes, usually therapeutic drug monitoring
would be just used for drugs with a narrow
therapeutic window.

However, for drugs with wide therapeutic window and high therapeutic index, there’s no need to
measure the plasma concentration because the toxic level is distant from the therapeutic level

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15
Q
A
16
Q

THERAPEUTIC DRUG MONITORING

Theophylline:
○ MEC: ________
○ MTC: ________

A

○ MEC: 7 - 10 mg/L
○ MTC: 15 - 20 mg/L

17
Q

THERAPEUTIC DRUG MONITORING

Some drugs’ effective doses against severe
infections are also with accompanying side effects (2)

A

anti-TB drug, anti cancer drugs

18
Q

THERAPEUTIC DRUG MONITORING

they cause hepatotoxicity,
that’s why patients are highly monitored

A

anti-TB drug

19
Q

THERAPEUTIC DRUG MONITORING

although they have
benefits, they can also cause toxicity

A

anti cancer drugs

20
Q

PHARMACOKINETIC VARIABLES

Compliance of patient is important

A

. ABSORPTION

21
Q

PHARMACOKINETIC VARIABLES

Variation in bioavailability are usually due to
variation in metabolism during absorption

A

ABSORPTION

22
Q

PHARMACOKINETIC VARIABLES

. Most important parameter in designing dosage
regimen

A

CLEARANCE

23
Q

PHARMACOKINETIC VARIABLES

Creatinine clearance

A

CLEARANCE

24
Q

CREATININE CLEARANCE:
Good indicator of (renal/liver) function

A

Renal

25
Q

CREATININE CLEARANCE
Not reliable indicator for (renal/liver) function

A

liver

26
Q

PHARMACOKINETIC VARIABLES

VOLUME OF DISTRIBUTION:
binding to plasma proteins
- ↓ Vd
- ↑ Vd

A

↓ Vd

27
Q

VOLUME OF DISTRIBUTION:
binding to tissues
- ↓ Vd
- ↑ Vd

A

↑ Vd

28
Q

VOLUME OF DISTRIBUTION:
drug distributed to body waters, extracellular
accumulation of body fluids
- ↓ Vd
- ↑ Vd

A

↑ Vd

29
Q

PHARMACOKINETIC VARIABLES

Clearance and volume of distribution

A

HALF LIFE