Introduction to pharmacology Flashcards

Taught by Mam. Kencho UNIT 1

1
Q

Define pharmacology?

A

Pharma: means drug or poison
Logy: Is the study
Pharmacology is the study of actions of drug on living organisms including chemical and physical properties, biochemical and physiological effects, mechanism of actions, therapeutic uses and adverse effects, of the drugs.

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2
Q

What are drugs?

A

Drugs are derived from the french word Drouge (dry herbs)
Drugs are chemicals that effects the processes of living organisms

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3
Q

What are the sources of drugs?

A

There are two sources of drugs.
1. Natural Sources
2. Synthetic

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4
Q

What are natural source drugs?

A
  1. Plants: morphine, atropine, digoxin, quinine
  2. Animals: Insulin, heparin, antitoxic sera
  3. Minerals: MGSO4, gold, iron, sulphur
  4. Microorganisms: Cephalosporins, tetracycline, penicillin
  5. Humans: Immunoglobulins, growth hormone
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5
Q

Synthetic source of drugs

A

Obtained from cell culture, recombinant DNA technology
Eg: Quinolones, Omeprazole, sulfonamide

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6
Q

Nomenclature of the drugs

A
  1. The chemical name: it is the technical description of the actual molecule and also referred as IUPAC id
  2. The generic name or the non property name: Official medical name accepted by the competent scientific body
  3. The brand name: The name assigned by the manufacture and the name in which the product is marketed
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7
Q

What is pharmacokinetics?

A

It means what body does to the drug or the quantitative study of drug movement in, through and out of the body by following processes: Absorption, distribution, metabolism and excretion also bioavailability.

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8
Q

Wat is absorption

A

It is the movement of drug from the site of administration to the circulation (speed of drug action = rate of absorption)

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9
Q

What determines absorption?

A
  1. Aqueous solubility
    rate of dissolution governs rate of absorption except in drugs given through IV
  2. Concentration
    Passive transport depends on concentration. Drugs given in concentrated solution absorbs faster than the drugs given in dilute solution
  3. Area of absorbing surface
    Larger the surface area, faster the absorption
  4. Vascularity of absorbing surface.
    Increased blood flow hastens the absorption
  5. Route of administration
    Fastest (Liquid, elixirs, syrup) Slowest (Enteric coated tablets)
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10
Q

Bioavailability

A

Refers to the rate and extent of abasorption of administered drug from ints dosage form determined by circulation time curve in the blood and excretion in urine
It is also the measure of fraction of administered dose of drug that reaches the systemic circulation in unchanged form

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11
Q

What is distribution

A

When the drug reaches the pblood system, it gets distributed to the other tissues.
Concentration gradient being from plasma to tissue.

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12
Q

What is the extent of distribution determined by

A

Lipid solubility
Ionization of physiological pH
Extent of binding of plasma and tissue proteins
Differences in regional blood flow
Body mass ratio and disease conditions

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13
Q

What is metabolism

A

Metabolism is also known as biotransformation and it means chemical alterations of drug in the body
An essential pharmacokinetic process is that it needs to make lipid soluble and non polar compounds into water soluble and polar compounds so they are excreted by various process from the body

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14
Q

What is the primary and other side of metabolism?

A

Primary side of metabolism is LIVER and others are plasma, kidney, intestine and lungs

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15
Q

What does metabolism lead to?

A
  1. Inactivation
  2. Active metabolite from active drug
  3. Activation from an inactive drug
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16
Q

First Pass Metabolism

A

Phenomenon of drug metabolism at a specific location in the body which leads to the reduction in the concentration of the active drug before it reaches the site of action

17
Q

What is excretion?

A

Excretion means removal of medication from the body

18
Q

what is t1/2 life

A

time taken for the plasma concentration of the drug to reduce to half of it’s value

19
Q

significance of t1/2 life

A
  1. Duration of action of drug
  2. Frequency of administration
  3. Time needed for action - steady state concentration
  4. To calculate loading and maintenance doses
20
Q

What is biological half life

A

It is the time required for total amount of drug in the body to be reduced to half.

21
Q

What is drug dose

A

it is an appropriate amount of drug needed to produce a certain degree of response in a patient

21
Q
A
21
Q

Factors determining dosage

A
  1. Age
  2. Sex
  3. Body weight and surface area
  4. Specific disease conditions
  5. Half life
  6. Tolerance
22
Q

What is pharmacodynamics?

A

What drug does to the body.
IT includes the physiological and biochemical effects of drugs and their mechanism of action

23
Q

what are the principles of drug actions or pharmacodynamics

A
  1. Irritation
  2. Depression
  3. Stimulation
  4. Cytotoxic action
  5. Replacement
24
Q

What are the mechanisms of drug action

A

Physical action - Absorptive property of charcoal
chemical action - chelating, acidifying, alkalinizing
through enzymes - enzymes are important target of drug action through either inhibition or stimulation
Through receptors - drugs chemically bind to specific site receptor sites

25
Q

What are agonist, antagonist and partial agonist

A

Agonist - Drug fits at receptor site well
Antagonist - Chemically block another chemical from getting to a receptor
Partial agonist - Attach to the receptor but only provide small effect

26
Q

What are the basic drug action

A

Desired action - expected response of the medication
Side effects - Known and frequently experienced or expected reactions to the drug
Adverse effect - Unexpected, unpredictable reactions that are not related to usual effect of normal dose of the drug

27
Q

What is adverse drug reactions or ADR?

A

Are any reactions that is unexpected, undesirable and occurs doses normally used and are not preventable

28
Q

Roles of nurses in ADR

A
29
Q
A