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31 Cards in this Set
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- 3rd side (hint)
What is a drug? |
Substance intended for use in diagnosis, cure, treatment, or prevention of disease. Substance with a physiological effect when introduced into the body. |
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Dose |
Quantity of a medicine or drug taken at a particular time Total mg or mg/kg |
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Bioequivalence |
Same active pharmaceutical ingredient (api) at the same concentration and in the same dose form. Equivalent pharmacokinetics and efficacy |
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Dosage |
Quantity and frequency of a dose of medicine or drug Mg/kg/day or mg/kg every 12 hours |
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Dosage regimen |
Includes route of administration and duration of dosing Mg/kg intravenously every 12 hours for 7 days |
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Pharmacodynamics (PD) |
Study of the physiologic effects of drugs and the mechanism of action What a drug does to the body |
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Pharmacokinetics (PK) |
Absorption, distribution, metabolism and excretion What the body does to a drug |
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Pharmacogenomics |
Study of how genes affect responses to drugs |
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Chemotherapy |
Effect of drugs upon microorganisms, parasites and neoplasticism cells living and multiplying in a living organism Includes: antibacterial, antiviral, antifungal drugs Antipatasitic drugs Cancer therapy |
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Toxicology |
Study of the undesirable effects of chemicals on living systems |
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Side effects |
Drug action outside the desired site (may be good or bad) |
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Adverse drug reaction |
Change in the patient |
Used interchangeably with adverse drug effect |
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Adverse drug effect |
The effect of the drug |
Used interchangeably with adverse drug reaction |
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Adverse drug event |
An adverse outcome that occurs while a patient is on a drug (causality not yet determined. May or may not be related to drug) |
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Affinity |
Force of attraction between a drug and a receptor Higher affinity=harder to displace |
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Selectivity |
Specificity of the drug for the target receptor binding |
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Potency |
Comparative term... Concentration of different drugs necessary to induce the same magnitude of response |
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Efficacy (intrinsic activity) |
Ability of a drug to have a response |
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Agonist |
Binds to receptor and enhances activity |
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Partial agonist |
Binds to a receptor and only partially enhances response |
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Antagonist |
Binds to a receptor to stop response and not allow other molecules to bind |
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Competitive antagonist |
Binds to the same site on the receptor not allowing other molecules to bind |
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Non-competitive antagonist |
Binds to a site on the receptor that changed it’s conformation, not allowing other molecules to bind anymore |
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Reversible antagonist |
Binds to a receptor but can easily dissociate from it. Weak bonds like H-binds and can see waals |
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Irreversible antagonist |
Binds to a receptor and stays there Strong bonds like covalent bonds |
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Inverse agonist |
Bind to a receptor and cause a “negative” response |
Or reverse agonist |
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Chemical antagonism |
Direct chemical interaction between two drugs (Ex: weak acid and weak base) |
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Physiologic antagonism |
Two drugs act in the same physiologic system but act on different receptors or pathways |
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Pharmacokinetic antagonism |
One drug alters the response to another drug through changes in disposition |
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Lipophilocity |
How soluble a drug is in fats/oil |
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Hydrophilicity |
How soluble a drug is in water |
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