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38 Cards in this Set

  • Front
  • Back
Drug
Chemical capable of producing a biological effect
Pharmacology
The study of mechanisms of drug action
Pharmacokinetics
What does the body do with the drug?

Absorption
Distribution
Metabolism
Excretion
Pharmacodynamics
What does the drug do to the body?
Toxicology
The study of poisons and harmful effects of drugs
Therapeutics
Treating disease with drugs
Pharmacy
Preparation, dispensing, and use of drugs
Pharmacognosy
Drug extraction from natural products
Pharmaceutics
Formulation of drugs
Drug Sources
Plants (Alkaloids)
Animals (Hormones)
Minterals
Synthetics
Tablets/Capsules
Active constituents with inert ingredients
Enteric Coatings
Polymers that will not disintegrate in gastric acid but will break down in the more alkaline intestines
Syrup
Sweetened aqueous solution
Elixir
Sweetened aqueous-alcoholic solutions
Enteral Administration
Oral, Rectal, Buccal, Sublingual
Parenteral Administration
Intravenous (IV), Intramuscular (IM), Subcutaneous (SC), Intrathecal, Intra-articular
Intrathecal Administration
Injection of a drug through the theca of the spinal cord into the subarachnoid space
Intra-articular Administration
Injection of a drug into a joint
Chemical Name
Specifies the chemical structure of the drug w/standard chemical nomenclature
Nonproprietary/Generic Name
Determined by the United States Adopted Names Council (USAN). Most appropriate for use in clinical practice.
Proprietary/Trade/Brand Name
Registered trademark belonging to a particular drug manufacturer and used to designate a drug product marketed by the manufacturer.
Primary Routes of Administration
Enteral, Parenteral, Transdermal, Inhalational, Topical
Routes That Avoid First Pass Hepatic Metabolism
Transdermal, Sublingual, Parenteral
Weak Acid
Chemical that is NOT charged when it is protonated

Only absorbed when protonated
Weak Base
Chemical that IS charged when it is protonated

Only absorbed when NOT protonated
pKa
the pH at which equal amounts of drug are charged and uncharged
Volume of Distribution (Vd)
The volume of fluid in which a drug would need to be dissolved to have the same concentration in that volume as it does in the plasma
Cp0
Concentration in plasma at time zero
Phase I Biotransformation
Oxidation, hydrolysis, or reduction
Phase II Biotransformation
Conjugation
Prodrugs
Administered as inactive compounds, but become active metabolites after biotransformation
Drug Biotransformation
Enzymatic metabolism of drugs to terminate the effect of a xenobiotic, or to activate a prodrug
Phase I Biotransformation
Oxidation, Hydrolysis, Reduction
Phase II Biotransformation
Conjugation
Influences of Drug Biotransformation
Genetics, Age, Pathology, Other Drugs
3 Phases of Renal Excretion
Glomerular Filtration, Active Tubular Secretion, Tubular Re-Absorption
Routes of Excretion
Renal (most), Biliary (high molecular weights), sweat, saliva
First Order Elimination Kinetics
Fraction of drug is removed per unit time.

Dependent upon plasma drug concentration.