Intro to pcol Flashcards

1
Q

It is the study of substances that interact with
living systems through chemical processes.

Occurs by binding of substances to regulatory
molecules and activating or inhibiting normal body processes.

A

Pharmacology

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2
Q

It is the science of substances used to prevent,

diagnose and treat diseases.

A

Medical Pharmacology

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3
Q

Branch of Pharmacology that deals with the
undesirable effects of chemicals on living
systems, from individual cells to humans to
complex ecosystem.

A

Toxicology

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4
Q

It refers to the effects of chemicals on all
organism and their survival in groups and as a
species

A

Environmental Toxicology

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5
Q

It focuses on the Familial-induced hepatic drug
reaction where affected individuals show an
abnormal adverse response to a class of drug.

A

Pharmacogenetics

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6
Q

It refers to the relation of an individual’s genetic
make up to his/her response to specific drugs.

It also refers to the difference of individuals with
their response to therapeutic drugs that can be
predicted from their genetic make-up.

A

Pharmacogenomics

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7
Q

It is concerned with the variability of drug effects

between individuals and at a population level.

A

Pharmacoepidemiology

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8
Q

Is the branch of economics that aims to quantify
in economic terms the cost and benefit of drugs
that are used therapeutically.

A

Pharmacoeconomics

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9
Q

T or F
All substances under certain circumstances can
be toxic

A

True.

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10
Q

T or F
The chemicals in botanicals whether herbs or
plant extracts are no different from chemicals in
manufactured drugs except for much greater
portion of impurities in manufactured drugs.

A

False

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11
Q

T or F
All dietary supplements and therapies promoted
as health-enhancing should meet the same
standards of efficacy and safety as conventional
drugs and medical therapies.

A

True

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12
Q

defined as any substance that brings about a

change in biologic function through its chemical actions.

A

Drug

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13
Q

Many drugs found in nature are

A

alkaloids

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14
Q

Most of the drugs would have a molecular

weight between

A

100 MW – 1000 MW

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15
Q

MW of Li ion

A

7

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16
Q

This also determines the ability of the
drugs to pass the blood brain barrier as
well as the placental barrier.

A

Drug size

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17
Q

Drugs interact with receptors by means

of

A

chemical forces or bonds.

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18
Q

strongest and

irreversible bond

A

covalent

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19
Q

more common but
weaker than covalent
bond.

A

Electrostatic

20
Q
weakest and important 
in the interactions of 
highly lipid-soluble drugs 
with lipids of cell 
membranes.
A

Hydrophobic

21
Q

Complementary to the of the receptor site
in the same way that the key is
complementary to that of the receptor
site.

A

Drug shape

22
Q

Carvedilol has how many isomers?

23
Q

Action (or effect) of the drug to

the body

A

Pharmacodynamics

24
Q

It describes the effect of the body

to the drugs

A

Pharmacokinetics

25
A drug that would activate the receptor
Agonist
26
Competes with or prevent the binding of | the molecule
Antagonist
27
It binds to the different receptors other | than the agonist.
Allosteric Agonist
28
It binds to the different receptors other | than the antagonist.
Allosteric Antagonist
29
Selective (to avoid constant activation) and changes its function upon binding that the function of the biologic system is altered
Receptors
30
Diphenhydramine is highly selective to __ receptor and Ranitidine highly selective to __ receptor.
H1;H2
31
site which is a non-regulatory molecule such as albumin that would result in no detectable change in the function of the biologic system.
Inert Binding Sites
32
activate receptor systems to the | maximum event of which the system is capable
Full agonist
33
bind to the same receptors and activate them in the same way but do not evoke great a response, no matter how high the concentration
Partial agonist
34
drug will reduce constitutive activity, resulting in effects that are opposite of the effects produced by the conventional agonist at the receptor.
Inverse agonist
35
T or F In the case of drugs that bind covalently to the receptor site, the effect may persist until the drug-receptor complex is destroyed and new receptors or enzymes are synthesized
True
36
o Route of administration o entrance of drugs remote to the site of target tissue or organ
Absorption
37
Determinants of distribution:
Size of the organ, blood flow, solubility, binding
38
Mechanism of | Activation or Termination of Drug Action
Metabolism -termination of drugs before excretion as they are metabolized to biologically inactive metabolites
39
a process wherein drugs continue to act until they are | excreted
Drug Elimination without Metabolism
40
Most of the metabolism occurs in the liver with the help of _______ enzyme.
cytochrome P450
41
T or F | Elimination is a process similar to excretion
False
42
For most drugs and their metabolites, excretion is primarily by way of the _____
kidney
43
are secreted primarily by the | lungs.
Volatile anesthetic gases
44
rate of elimination is | proportional to the concentration.
First Order Elimination
45
rate of elimination is | constant regardless of concentration.
Zero Order Elimination
46
T or F | In Zero Order Elimination, concentration of drugs in plasma increases in linear fashion over time
False
47
T or F | Si Quen ay ubod ng ganda
True