| Term 
 
        | pharmaceutic phase   Tablet and capsules     |  | Definition 
 
        | the dissolution of the drug, and what types of durgs go through this phase? |  | 
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        | Term 
 
        | Pharmokenetic Phase tablets and capsuls, liquid and parenteral drugs |  | Definition 
 
        | what the body does to the drug, a drugs activity from the time it enters the body untill it leaves. and what type of drugs go through this phase? |  | 
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        | Term 
 
        | Absorbtion Distribution Metabolism excreation half-life                 |  | Definition 
 
        | in the pharmocokinetic phase what are the activities of a drug |  | 
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        | Term 
 | Definition 
 
        | the transference of drug molecules from point of entry in the body into the blood system |  | 
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        | Term 
 | Definition 
 
        | protein or enzyme move drug across cell membrane |  | 
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        | Term 
 | Definition 
 
        | diffusion: from high to low |  | 
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        | Term 
 | Definition 
 
        | engulfing drug particle to move across cell |  | 
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        | Term 
 
        | active absorbtion,Passive absorbtion, and pinocytosis |  | Definition 
 
        | what are the way of absorbtion for a solid drug |  | 
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        | Term 
 
        | route of administration Drug solubility PH local conditions at site of administration Drug dosage serum dug levels |  | Definition 
 
        | what are the factors that influence rate of absorbtion |  | 
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        | Term 
 
        | IV imediate IM SC PO then other absorbtive sites, skin, vagina,rectum,eyes |  | Definition 
 
        | What are the routes of administration in order most rapid first? |  | 
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        | Term 
 | Definition 
 
        | this type of drug must have affinity for water- Passes through cell membranes thru water channels Ex. Vitamins, (pass readily) |  | 
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        | Term 
 | Definition 
 
        | This type of drug is non-ionized is absorbed readily but remains in fatty tissue, Not easily distributed Ex: Valium |  | 
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        | Term 
 | Definition 
 
        | A_________medication will be more readily absorbed in the stomach Ex: ibprophen |  | 
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        | Term 
 | Definition 
 
        | a_______________medication will not be absorbed untill it reaches the small intestine |  | 
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        | Term 
 | Definition 
 
        | a decrease in the size of an organ or tissue |  | 
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        | Term 
 | Definition 
 
        | a larger than normal dose given when maximal and quick effect is desired |  | 
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        | Term 
 | Definition 
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        | Term 
 
        | therapeutic (effect) range |  | Definition 
 
        | the desiredeffect in blood without toxicity, the desired concentration in blood serum |  | 
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        | Term 
 | Definition 
 
        | highest plasma concentration of drug after complete absorbtion. This is measured when complete absorbtion has been achieved. |  | 
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        | Term 
 | Definition 
 
        | when drug is at the lowest level this is drawn 30min before next dose |  | 
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        | Term 
 | Definition 
 
        | amt of time it takes for half a dose of a drug to be elimenated from the body |  | 
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        | Term 
 | Definition 
 
        | transportation from site of absorbtion to site of action is called? |  | 
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        | Term 
 
        | depends on physical and chemicalproperty of the drug (water or lipid soluable) and wheather drug has protien bonding copasity |  | Definition 
 
        | what are the factors affecting distribution? |  | 
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        | Term 
 | Definition 
 
        | Difficult to pass, permits lipid bound meds, and prevents water soluable meds |  | 
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        | Term 
 | Definition 
 
        | easieier passage of meds permits lipid souluable drugs to enter fetal circulation, prevents other meds from crossing? |  | 
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        | Term 
 | Definition 
 
        | most drugs are bound to__________ |  | 
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        | Term 
 | Definition 
 
        | available to cross cell membrane |  | 
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        | Term 
 | Definition 
 
        | not available for pharmacological action |  | 
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        | Term 
 | Definition 
 
        | the process  of inactivating and breaking down a med |  | 
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        | Term 
 | Definition 
 
        | primary site: the first-pass effect |  | 
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        | Term 
 | Definition 
 
        | enzymes in liver,lungs, kidneys,GI,skin break down med into? |  | 
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        | Term 
 | Definition 
 
        | what are the factors effecting metabolizm |  | 
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        | Term 
 | Definition 
 
        | enzyme system mature slowly |  | 
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        | Term 
 | Definition 
 
        | this type of person decrease overall metabolic capacity of liver ( toxicity at normal doses) |  | 
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        | Term 
 | Definition 
 
        | the process where the metabolites and drugs are elimenated |  | 
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        | Term 
 | Definition 
 
        | the main organ for drug elimenation |  | 
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        | Term 
 | Definition 
 
        | the time requried for the body to eliminate 50% of the drug |  | 
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        | Term 
 | Definition 
 
        | it takes _______half lives to elimiate 98% of adrug from a body |  | 
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        | Term 
 | Definition 
 
        | what the drug does to the body, the drug action and effect within the body. There is alteration of cell physiology |  | 
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        | Term 
 | Definition 
 
        | causes an increase of decrease in certain physiological function(hr,BP, urinary output) |  | 
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        | Term 
 | Definition 
 
        | the unintended effect of a drug |  | 
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        | Term 
 | Definition 
 
        | the decrease physiologic response of the body to a drug, requireing an increase in dosage to achievew the desired effect. |  | 
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        | Term 
 | Definition 
 
        | when rate of administration exceeds rate of metabolism |  | 
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        | Term 
 | Definition 
 
        | this is harmful reactions on tissues or organs   |  | 
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        | Term 
 | Definition 
 
        | the unusual, abnormal, or pecular reaction to a drug cause not clear |  | 
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        | Term 
 | Definition 
 
        | devepmental defects of a drug in the embryo or fetus |  | 
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        | Term 
 | Definition 
 
        | effects occure when 2 drugs with similar pharmocologicalactions are taken together |  | 
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        | Term 
 | Definition 
 
        | occures when 2 drugs with different pharmacological actions produced greater effects when taken together then either dose when taken alone ex: tylenol w codien |  | 
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        | Term 
 | Definition 
 
        | one drug interfers with the action of others, neutralizes or decreases effect of other ex: protamine sufate on heparine narcan on a narcotic |  | 
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        | Term 
 | Definition 
 
        | inappropriate intake of a substance |  | 
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        | Term 
 
        | generic drug nomenclature |  | Definition 
 
        | name given to a drug, less expensive |  | 
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        | Term 
 | Definition 
 
        | brand or proprietary name, 1st letter always capitolized |  | 
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        | Term 
 
        | controlled release sustained release slow actiog long acting time released |  | Definition 
 
        | name these abbreviation for types of drugs CR SR SA LA TR |  | 
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        | Term 
 
        | down &back straight & back up & back |  | Definition 
 
        | ways to give ear drops infant-3? school age? adult? |  | 
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        | Term 
 
        | anagesic, antipyretic,and anti-anflamatory |  | Definition 
 
        | pharmacological effects of salicylates (ASA)? |  | 
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        | Term 
 
        | by dialating peripheral blood vessels |  | Definition 
 
        | how do salicylates decrease body temp. |  | 
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        | Term 
 
        | it prolonges the bleeding time by inhibiting the aggregation (clumping)of platlets |  | Definition 
 
        | what effects does ASA have on bleeding |  | 
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        | Term 
 
        | relieving mild to moderate relieves elevated body temp tx inflamatory conditions reducing clots and strokes helps haintain pregancy |  | Definition 
 
        | list common uses of salicylates |  | 
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        | Term 
 
        | gi bleeding,gi upset,anorexia, nausea, allergic reaction,heartburn,vomiting |  | Definition 
 
        | adverse reactions with ASA |  | 
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        | Term 
 | Definition 
 
        | over dose of Salycilic meds, characterized by dizzyness,impaired hearing, Tinnitus nasua, vomiting, tacycardia, sweating, rapid deep breathing, mental confusion, possile coma is called |  | 
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        | Term 
 | Definition 
 
        | non-opioid analgesic inhibits platelet aggression, is an anaglgesic of choicewhen bleeding tendencys is an issue antipyretic |  | 
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        | Term 
 
        | liver, and tx, is macromyst(gastric Lavage) |  | Definition 
 
        | toxicity from nonsalycitates (acetaminaphen) effects what organ and what is the tx? |  | 
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        | Term 
 
        | charchole and gastric lavage |  | Definition 
 
        | what is the tx for salicylate overdose? |  | 
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        | Term 
 | Definition 
 
        | morphine, codine, hydrochlorides are all? |  | 
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        | Term 
 
        | synthetic narcotic agents |  | Definition 
 
        | methadone, levorphanol, and remifentanil are all? |  | 
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        | Term 
 
        | analgesic, antipyretic,and anti inflammatory |  | Definition 
 
        | phamscological effectsof NSAIDS? |  | 
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        | Term 
 
        | patient controlled anagesic |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Has a Long lasting and systemic effect |  | 
        |  |