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39 Cards in this Set

  • Front
  • Back
Def of Potency
Amount of a drug needed to produce effect
Def of Efficacy
Maximum intensity of effect or response that can pe produced by a drug. (regardless of dose)
Example of Potency vs. Efficacy
Ingesting enough of either whiskey or beer can cause a person to be drunk or unconcious.

They have the same EFFICACY (drunkeness), but their POTENCIES differ because less whiskey is required to produce the same result as several beers
Def of ED50 (3)
Example
1) Dose of a drug required to produce a specific effect in 50% of subjects

2) Dose that produces half the maximum effict

3) The higher the potency of a drug, the lower the ED50 will be

EX. meperidine (100mg) equals morphine (10mg)
Def of LD 50 (lethal dose)
Dose when half of the subjects die
When drugs are distributed to their site of action, the elicit a _________ effect.

Drugs _______ _____ _____ _____ as an endogenous agent in the body or they ______ ____ ______ of an endogenous agent in the body.
They DO or DO NOT impart a new function???
When drugs are distributed to their site of action, the elicit a PHARMACOLOGIC effect.

Drugs PRODUCE THE SAME ACTION as an endogenous agent in the body or they BLOCK THE ACTION of an endogenous agent in the body.
They DO NOT impart a new function???
Neurotransmitter sends message across a ________.
The neurotransmitter interacts with a _______. They fit together like a puzzle.
Then an ______ is signaled to be activated.
Neurotransmitter sends message across a NERVE SYNAPSE.
The neurotransmitter interacts with a RECEPTOR. They fit together like a puzzle.
Then an ENZYME is signaled to be activated.
6 Examples of Neurotransmitters
1) acH (acetylcholine)
2) norepinephrine / epinephrine
3) dopamine
4) serotonin
5) GABA
6) histamine
Drugs can combine with a ________ to alter the function of the organism, either by _______ or ________ the function.
Drugs can combine with a RECEPTOR to alter the function of the organism, either by ENHANCING or INHIBITING the function.
Def of Agonist

Note: Naturally occuring __________ are agonists.
A drug that has an affinity for a receptor, combines with the receptor, and produces an effect.
Note: Naturally occuring NEUROTRANSMITTERS are agonists.
Def of Antagonist
A drug that counter acts the action of the agonist.
3 Types of Antagonists
1) Competitive
2) Noncompetitive
3) Physiologic
Routes of administration affects?
Affects the onset & duration of response.
Def of Enteral
Drug is placed directly into the GI tract by oral or rectal.
Def Parenteral
Drug given bypasses the GI tract by injection, inhalation, topical, etc. (usuallly refers to injection)
2 Types of Enteral Drugs
1) Oral

2) Rectal
Oral drugs (9 facts)
1)Common, most popular, simplistic, safe
2) May cause nausea and stomach irritation
3) Some drugs can't be given this way, because of acidity or enzymes in GI tract.
4) Small intestine has a large absorbing area
5) Initially passes through the liver
6) Can inactivate some drugs
7) Termed first pass effect
8) Drugs w/ a high first-pass effect have a larger oral-to-parenteral dose ratio
9) Drugs interactions can occur whtn 2 drugs are present in the stomach
Rectal drugs (2 facts)
1) useful if patient is vomitting or unconscious

2) Poor absorption & poor compliance
8 Types of Parenteral Drugs
1) Intravenous
2) Intramuscular
3) Subcutaneous
4) Intradermal
5) Intrathecal
6) Intra peritoneal
7) Inhalation
8) Topical
Intravenous Drug (2 facts)
1) Most rapid drug reponse with immediate onset.

2) Best for emergencies
Intramuscular Drugs (2 facts)
1) usually in deltoid or gluteal mass.
2) irritating drugs better tolerated in this route
Other Parenteral Drug Examples
- Subcutaneous
- Intradermal
- Intrathecal
- Intra peritoneal
- Inhalation
- Topical
- Subcutaneous --> insulin
- Intradermal --> TB skin
- Intrathecal --> the space under the arachnoid membrane of the brain or spinal cord
- Intraperitoneal --> injection into the peritoneum (body cavity).
- Inhalation --> asthma, NO2
- Topical --> acne
Topical route
Through skin, oral mucosa, sublingually
Topical route
- 1 fact
- 7 examples
1) most drugs do not penetrate intact skin

Examples
1) Local anesthetic gel or spray
2) Sublingual nitroglycerine
3) Sublingual strips & gels (Periochip)
4) Transdermal patch
5) Lidocaine patch
6) birth control patch
7) creams
Def of pharmacokinetics
The study of how a drug enters, circulates, is changed, and leaves the body.

Includes absorption, distribution, metabolism and excretion.
Def of Absorption
Process by which drug molecules are transferred from the site of administration to the circulating blood.

This process requires the drug to pass through biologic membranes.
Absorption is Effected by ...
Physicochemical factors, site of absorption, distribution, metabolism, and excretion.
Drugs are found in the blood in 2 forms..
1) Bound

2) Free
Free drug in blood
- Is what...?
- Can pass where?
Exerts (puts into use) the pharmacologic effect

Can pass across cell membrane
Bound drug in blood
- Is a...?
Is a reservoir for the drug.
Distribution
- definition
- allows...?
- effects...?
Def = the passage of drugs into various body fluid compartments.

Allows a drug to be made available at its site of action so that it can exert it activity.

Effects how rapidly the drug produces a desired reponse & duration.
Distribution
- occurs...?
Occurs when a drug moves to various sites in the body.
Both to the site of action & to non-specific tissues where no action is desired.
Distribution
- effected by...? (5)
Effected by:
1) size of organ
2) blood flow to organ
3) solubility of drug
4) plasma protein binding capacity
5) presence of barriers
Metabolism
- definition
- where?
Def = Bodies way of changing a drug so that it can be more easily excreated

Where = Most commonly this transformation takes place in the Liver
Route of drug excreation
1) renal (kidney) - most important
2) lungs
3) bile
4) GI tract
5) sweat
6) saliva
7) breast milk
...Drugs can be excreated unchanged or metabolized
Factors altering drug effects (11)
1) patient compliance
2) phycological factors
3) tolerance (need for increasingly larger doses)
4) pathology (liver and kidney disease)
5) time of administration
6) route of administration
7) gender
8) genetic variation
9) drug interactions
10) age / weight
11) Environment (smoking induces enzymes)
Calculation of children's dose (3)
1) Weight

2) Age

3) Surface area (fx of weight & height)
Half Life
- Def of
- 2 Types
Amount of time it takes for the concentration of a drug to fall to half of its level in the blood.

Types
1) short half life = short duration
2) long half life = long duration
If the half life is 30 mins.

After 30 min ___% of the drug remains.

After another 30 min, half of the __% = __% remains

After another 30 min, half of the __% = __% remains

By __ or __ half lives the drug is gone.
If the half life is 30 mins.

After 30 min 50% of the drug remains.

After another 30 min, half of the 50% = 25% remains

After another 30 min, half of the 25% = 12.5% remains

By 4 or 5 half lives the drug is gone.