| Term 
 | Definition 
 
        | scientific name, describes atomic, molecular structure |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Trade (brand, proprietary) name |  | Definition 
 
        | selected by drug company, copyright protected |  | 
        |  | 
        
        | Term 
 
        | 1962, Federal government mandated use of one official name per drug Listed in:
 United States Pharmacopeia
 National Formulary
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | groups drugs with similar characteristics |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | groups drugs by therapeutic use |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Plants, Animals, Minerals |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Metallic, non-metallic [iron, iodine, Epsom salts] |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Hormones [insulin], oils [cod liver oil], enzymes [pancreatin, pepsin], vaccines [micro-organisms] |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Alkaloids [caffeine, nicotine], glycosides [digoxin], gums [seaweed extractions], resins, oils [peppermint, castor oil] |  | 
        |  | 
        
        | Term 
 
        | synthetically made in laboratory |  | Definition 
 
        | Isolate and intensify active component Manipulate molecular structure
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Method influences the Quantity given
 Absorption rate
 Distribution in body
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Oral (PO): patient conscious, can swallow; drug withstands stomach acids |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | into capillary bed under tongue |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | in pouch between cheek and gum |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Rectal (PR), vaginal: suppositories, ointments, creams, gels |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | gases rapidly absorbed; metered-dose inhaler |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | local delivery through skin, mucous membrane [dermatologic, ophthalmic, nasal preparations] |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | “patch” applied to skin, drug enters blood through capillaries |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | “patch” applied to skin, drug enters blood through capillaries |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | directly into GI system, patient can’t ingest orally |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | : injected into skin (dermis) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | * Intravenous (IV): rapid onset, injected directly into blood |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Intramuscular (IM): injected into muscle; drug enters blood through capillaries |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Subcutaneous (SubQ, SC): injected into subcutaneous tissue; drug enters blood through capillaries |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Investigational New Drug (IND): new drug application after animal studies prove safety, effectiveness |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Phase I: tested on healthy volunteers Phase II: tested on people with specific disease
 Phase III: more people, look for adverse effects
 Phase IV: post-market surveillance; reports from doctors on therapeutic or adverse effects
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | New Drug Application (NDA): years later Treatment Investigational New Drug (treatment IND): expedited approval due to public health threat [AIDS drugs]
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Study of what happens from time drug enters body until it, and all its metabolites, leave body: |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | : rate drug leaves site of administration Fast: seconds, minutes (sublingual, IV, inhalation)
 Slow: (oral, IM, SC)
 Slowest: hours, days (rectally, sustained-release)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Influenced by: blood flow, stress, diet, drug formulation, drug-drug interaction |  | 
        |  | 
        
        | Term 
 
        | First-pass effect: liver metabolizes drug Oral drugs absorbed in small intestine - liver (first-pass effect)- circulated to rest of body
 |  | Definition 
 
        | May inactivate/lower amount of active drug released into circulation Necessitates higher oral drug dosage for desired effect
 |  | 
        |  | 
        
        | Term 
 
        | Distribution factors Drug delivery to site of action (body tissues, fluids)
 |  | Definition 
 
        | Blood flow: faster to heart, liver, kidneys; slower to internal organs, skin, fat, muscle Solubility: lipid-soluble cross cell membrane, blood-brain barrier; water-soluble don’t
 Protein binding: bound part therapeutically inactive; free (unbound) portion active
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Body changes drug from dosage form to excretable water-soluble form: Into inactive metabolites
 Into active metabolites with own pharmacologic action
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | inactive drugs, become active after metabolized |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Drug elimination from body: Kidneys -urine
 Lungs -exhalation
 Exocrine glands -sweat, saliva, milk
 Skin -sweat
 Intestinal tract -feces
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 50% of drug in blood eliminated every ½ life Helps determine dosage frequency
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Drug administration = drug excretion |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | time interval from drug administration to therapeutic effect |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | absorption rate = elimination rate |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | length of therapeutic effect |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Study of mechanism of drug action on biological system Drug forms chemical bond with specific receptor sites on surface of cell
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | initiate cell response after binding cell receptor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | incomplete binding, prevents cell response |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | : competes with agonist for receptor site; reversible binding |  | 
        |  | 
        
        | Term 
 
        | Antagonist Non-competitive: |  | Definition 
 
        | binds receptor, blocking agonist binding; irreversible binding |  | 
        |  |