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31 Cards in this Set

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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.

Dose

Quantity of a medicine or drug taken at a particular time


Total mg or mg/kg

Bioequivalence

Same active pharmaceutical ingredient (api) at the same concentration and in the same dose form.


Equivalent pharmacokinetics and efficacy

Dosage

Quantity and frequency of a dose of medicine or drug


Mg/kg/day or mg/kg every 12 hours

Dosage regimen

Includes route of administration and duration of dosing


Mg/kg intravenously every 12 hours for 7 days

Pharmacodynamics (PD)

Study of the physiologic effects of drugs and the mechanism of action


What a drug does to the body

Pharmacokinetics (PK)

Absorption, distribution, metabolism and excretion


What the body does to a drug

Pharmacogenomics

Study of how genes affect responses to drugs

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

Toxicology

Study of the undesirable effects of chemicals on living systems

Side effects

Drug action outside the desired site (may be good or bad)

Adverse drug reaction

Change in the patient

Used interchangeably with adverse drug effect

Adverse drug effect

The effect of the drug

Used interchangeably with adverse drug reaction

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)

Affinity

Force of attraction between a drug and a receptor


Higher affinity=harder to displace

Selectivity

Specificity of the drug for the target receptor binding

Potency

Comparative term...


Concentration of different drugs necessary to induce the same magnitude of response

Efficacy (intrinsic activity)

Ability of a drug to have a response

Agonist

Binds to receptor and enhances activity

Partial agonist

Binds to a receptor and only partially enhances response

Antagonist

Binds to a receptor to stop response and not allow other molecules to bind

Competitive antagonist

Binds to the same site on the receptor not allowing other molecules to bind

Non-competitive antagonist

Binds to a site on the receptor that changed it’s conformation, not allowing other molecules to bind anymore

Reversible antagonist

Binds to a receptor but can easily dissociate from it.


Weak bonds like H-binds and can see waals

Irreversible antagonist

Binds to a receptor and stays there


Strong bonds like covalent bonds

Inverse agonist

Bind to a receptor and cause a “negative” response

Or reverse agonist

Chemical antagonism

Direct chemical interaction between two drugs


(Ex: weak acid and weak base)

Physiologic antagonism

Two drugs act in the same physiologic system but act on different receptors or pathways

Pharmacokinetic antagonism

One drug alters the response to another drug through changes in disposition

Lipophilocity

How soluble a drug is in fats/oil

Hydrophilicity

How soluble a drug is in water