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39 Cards in this Set
- Front
- Back
Def of Potency
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Amount of a drug needed to produce effect
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Def of Efficacy
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Maximum intensity of effect or response that can pe produced by a drug. (regardless of dose)
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Example of Potency vs. Efficacy
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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 |
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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) |
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Def of LD 50 (lethal dose)
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Dose when half of the subjects die
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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??? |
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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. |
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6 Examples of Neurotransmitters
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1) acH (acetylcholine)
2) norepinephrine / epinephrine 3) dopamine 4) serotonin 5) GABA 6) histamine |
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Drugs can combine with a ________ to alter the function of the organism, either by _______ or ________ the function.
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Drugs can combine with a RECEPTOR to alter the function of the organism, either by ENHANCING or INHIBITING the function.
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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. |
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Def of Antagonist
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A drug that counter acts the action of the agonist.
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3 Types of Antagonists
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1) Competitive
2) Noncompetitive 3) Physiologic |
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Routes of administration affects?
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Affects the onset & duration of response.
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Def of Enteral
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Drug is placed directly into the GI tract by oral or rectal.
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Def Parenteral
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Drug given bypasses the GI tract by injection, inhalation, topical, etc. (usuallly refers to injection)
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2 Types of Enteral Drugs
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1) Oral
2) Rectal |
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Oral drugs (9 facts)
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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 |
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Rectal drugs (2 facts)
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1) useful if patient is vomitting or unconscious
2) Poor absorption & poor compliance |
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8 Types of Parenteral Drugs
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1) Intravenous
2) Intramuscular 3) Subcutaneous 4) Intradermal 5) Intrathecal 6) Intra peritoneal 7) Inhalation 8) Topical |
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Intravenous Drug (2 facts)
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1) Most rapid drug reponse with immediate onset.
2) Best for emergencies |
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Intramuscular Drugs (2 facts)
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1) usually in deltoid or gluteal mass.
2) irritating drugs better tolerated in this route |
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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 |
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Topical route
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Through skin, oral mucosa, sublingually
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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 |
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Def of pharmacokinetics
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The study of how a drug enters, circulates, is changed, and leaves the body.
Includes absorption, distribution, metabolism and excretion. |
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Def of Absorption
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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. |
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Absorption is Effected by ...
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Physicochemical factors, site of absorption, distribution, metabolism, and excretion.
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Drugs are found in the blood in 2 forms..
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1) Bound
2) Free |
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Free drug in blood
- Is what...? - Can pass where? |
Exerts (puts into use) the pharmacologic effect
Can pass across cell membrane |
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Bound drug in blood
- Is a...? |
Is a reservoir for the drug.
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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. |
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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. |
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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 |
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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 |
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Route of drug excreation
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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 |
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Factors altering drug effects (11)
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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) |
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Calculation of children's dose (3)
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1) Weight
2) Age 3) Surface area (fx of weight & height) |
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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 |
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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. |