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188 Cards in this Set
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- Back
A,D,M,E
Stands for what in Pharmokinetics? |
Absorption
Distribution Metabolism Excretion |
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Define Pharmokinetics
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Movement of drugs through the body including the process, absorption, distribution metabolism and elemination.
Quantitative, time dependent changes of both plasma drug concentration and the total amount of drug in the body following administration. |
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Define Excretion
In what ways can a drub be excreted? |
Elimination of medication from the body through....
Renal (Kidney), Deification, Perspiration, respiration, lactation and lacrimation |
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Define Absorption
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Transfer of drug from its site of administration to the blood stream.
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Define Pharmacodynamics
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The study of uptake movement, binding and interactions of pharmacologically active molecules at their tissue sites of action.
Biochemical and physiological effects of drugs and their mechanisms of their actions. Including correlation of their actions and effects with their chemical structure. |
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Define Metabolism
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Process by which the body chemically alters drugs through enzymatic action. (biotransformation)
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Define Distribution
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Process by which a drug reversibly leaves the blood stream and enter the intestitum. (extracellular fluid)
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Define Ionized
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Charged
Has + or - ig: K+ |
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Define Unionized
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Not Charged
No + or - ig: K |
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Define Pharmacology
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Science concerning with drugs, their sources, appearances, chemistry action and uses.
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Define
Pharmacodynamics |
The study of the physiological effects of drugs and the mechanism of their action on the body.
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Define
Therapeutic Dose |
The amount of medication required to produce the desired effect.
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Define
Half Life |
Duration of action of drug is known as its half life. It is the period of time required foe the concentration or amount of drug in the body to be reduced by one-half.
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Define
Maximum Effective Dose |
Largest dose which is able to give with safety
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Define
Minimum Effective Dose |
The smallest dose that will produce an appreciable effect.
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Define
Passive Diffusion |
Passage of electrolytes to all arts of a solution, including through a permeable membrane.
Absorption process that occures in the body when carbohydrates are more highly concentrated in the intestine that in the blood. Plays apart in intestinal absorption. |
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Define
Active Transport Mechanism |
Movement of ions or molecules across cell membranes and epithelial layers, AGAINST a concentration gradient with the use of metabolic energy. It requires ATP for metabolic energy.
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What is the chemical nature of a drug?
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Lipid Soluble
or Water Soluble |
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Define
Facilitated Diffusion |
Otherwise known as Passive Transport.
Mechanisms in which a carrier mechanism involving portent and active transport which provides energy from the breakdown of high energy phosphate bonds. |
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What is the mode of transportation across a membrane?
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Lipid soluble drugs needs Lipid Transporter at the blood level. It can't dissolve in water.
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Lipid Soluble drugs need?
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Lipid transporter
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Water Soluble drugs can be dissolved in?
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Blood
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Are water soluble drugs safer drugs?
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Yes
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Define
Unbound Drugs |
Pharmacology ACTIVE drug that can cross the membrane. The drug is not bound to to a carrier proven or molecule.
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Define
Therapeutic Index |
Ratio of toxic dose to the effective dose.
(TI) = Toxic dose / Effective Dose You look for a Narrow Therapeutic Index |
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Lipid Soluble drugs need what to work?..
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Lipid Transporters
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Are Lipid Soluble drugs More Toxic to the body?
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YES
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Can Lipid Soluble drugs dissolve in blood?
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NO
But they can pass through the cell membrane. |
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Acidic Drugs are?
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Ionized
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Alkaline Drugs are?
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NOT Ionized
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Define
Efficacy |
Measure of how well a drug produces a response.
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Define
Potency |
A measure of the activity of a drug in a biological system.
Shows relative doses of two or more agonist to produce the same magnitude of effect. |
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Define
Antagonist |
A drug is called an Antagonist when binding to the receptor is NOT associated with a response. The drug has a effect only by preventing an agonist from binding to the recpetor.
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Define
Agonist |
A drug is called agonist when binding to the rector results in a response.
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Define
Zero Order Elimination Rate |
A constant amount of drug is eliminated per unit time.
*Drugs with zero order elimination have NO fixed half life. 4hr. 4hr 4hr 4hr. 80mg --70mg--60mg--50mg--40mg |
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Define
First Order Elimination Rate |
A constant faction of the drug is eliminated per unit of time. (t1/2)
* Directly proportional to plasma level. Most common elimination of drug which has a rapid elimination rate. 4hr. 4hr. 4hr. 4hr. 80mg--40mg--20mg--10mg--5mg |
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Define
Steady State |
Steady state is reached either when RATE IN = RATE OUT.
when values associated with a dosing interval are the same as those in the succeeding interval |
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Define
Plateau Principle |
Time to reach steady state is dependent only on the elimination half life of a drug, and independent of dose size and frequency of administration.
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Define
Loading Dose Effect |
It takes 4-5 half lives to achieve steady state.
*Some situation it may be necessary to give a higher dose (loading dose) to more rapidly achieve effective blood levels. |
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Define
Placental Barrier |
Term used for the placental membrane because it prevents the assuage of some material between the maternal and fetal blood.
Most small molecular weight drugs cross the placental barrier. |
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Define
Blood-Brain Barriers |
Selective barrier separating the blood from the parenchyma of the central nervous system
Permeable only to lipid soluble drugs or those of very LOW Molecular weight. |
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Define
Biotransformation |
Metabolic conversion of drug molecules to more water-soluble metabolites that are more deadly excreated.
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Phase 1 Biotransformation
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Modification of the drug molecule via oxidation, reduction or hydrolysis.
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Phase 2 Biotransformation
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Conjugation with endogenous compounds via the activity of transferases
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Define
Absorption |
Process of entry of a drug into the systemic circulation from the site of administration.
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Define
Bioavailability |
Measure of the fraction of an administered dose that reaches the systemic circulation.
Ie: Intravascular doses have 100% bioavaliability. |
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Define
First Pass Effect |
mechanism whereby drugs are absorbed across the intestinal wall and enter into the hepatic portal circulation and initially distributed to the liver.
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Define
Distribution |
Process of distribution of a drug from the systemic circulation to organs and tissue.
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What are the 2 types of special barriers?
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Blood Brain
Placental |
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Nonionized drugs have what charge?
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Uncharged form
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Ionized druge have what charge?
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Have a positive and negitive charge.
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What modes of drug transport are there?
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Passive Diffusion - Down Gradient
Facilitated Diffusion - Down Gradient Active Transport - Against Gradient |
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Define
Concentration Gradient |
Diffusion down a concentration gradient.
only free unionized drug from contribute tot he concentration gradient. *Gradual change in concentration of solute in a solution. |
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Surface Area
and Vascularity |
Regards to absorption of drugs into systematic circulation.
the larger the surface area the greater the vascularity, the better the absorption of the drug. |
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Drug permeation is dependent on?
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Solubility
Concentration Gradient Surface area vascularity |
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Water Soluble drugs are?
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Ionized Drugs
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Lipid Soluble Drugs are?
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Nonionized Drugs
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Unbound drugs are?
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Active Drugs or compounds that are NOT bound to a carrier protein - Pharmacolgically Active.
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Active Drugs are considered what type of drugs?
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Unbound
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Define
Passive Diffusion |
Movement of material from an area of high concentration to and area with lower concentration.
*It does not require Active Transport. |
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Define
Solubility |
Ability to diffuse through lipid bilayers (Lipid Solubility)
*Important for most drugs- however water solubility can influence permeation through aqueous phase. |
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Define
Tolerance |
process of adapting to a drug over a period of time and subsequently require higher doses to achieve the same effect.
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Normal PH is?q
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7.0
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Base or Alkalinity is levels
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8-10 PH
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Acidity PH levels are
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6-0 PH
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Define
therapeutic Index |
Therapeutic agent that causes the therapeutic effect to the amount that causes death or toxicity.
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Define
Narrow Therapeutic Index |
Small changes in the dosage could cause toxic effects
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Define
Bioavailability |
The fraction of administered drug that reaches the systemic circulation
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Define
Half-Life |
(t1/2) The time required for the concentration of a drug to drop by 50%.
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Define
Steady State |
When the plasma concentration of a drug remains constant, the rate of elimination = rate of input.
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Define
Efficacy |
the maximal RESPONSE produced by a drug
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Define
Potency |
?how much drug is required to elicit a given response )increase potency=Decrease dose)
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Define
Agonist |
An agent that can bind to a receptor and elicit a response.
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Define
Partial-Agonsit |
An agent that block the binding site and causes less response than a true agonist.
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Define
Antagonist |
Interacts with receptor by produces no action of its own. It blocks the action of agonist.
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Define
Therapeutic Index |
The ration of toxic dose to the effective dose.
TI = Toxic dose/effective dose |
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Define
Volume of Distribution (Vd) |
A hypothetical volume expressing the relationship between the total amount of drug in the body and the concentration of drug in the blood.
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Superscription
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Contains the symbol Rx, meaning "take throu" or "recipe"
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Inscription
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Specifies the name and strength of the dug
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Signature or Sig
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Gives the directions for taking the medication and route of administration
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Subscription
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Gives directions to the pharmacist. It designates the # of doses, the quantity to be dispensed and the form of the drug.
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What should be included on all prescriptions?
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1: Preprinted with PA's Name, Address and phone number.
2: Patient heading includes the PATIENTS name, address, date when the prescription was written and the Patients age if a a child. 3: Contains symbol Rx 4: Specifies the name and the strength of the drug and quantity. 5: Signa: which gives directions for taking medication. 6: Subscription: gives direction to pharmacist to fill 7: Singnature of PA 8: Refill line. NEVER TO LEAVE BLANK! 9: Drug Enforcement Administration Number required for controlled substances |
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Pregnancy Category A
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Controlled studies show no risk.
No risk to fetus |
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Pregnancy Category B
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No evidence of rush in humans.
animal findings show risk but humans show no risk |
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Pregnancy Category C
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Risk cannot be ruled out.
Human studies lacking, animal studies show positive for fetal risk. Potential benefits may justify risk |
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Pregnancy Category D
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Postive evidence of risk.
proof of risk to fetus.May be acceptable in life threatening situations. |
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Pregnancy Category X
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Contradicted in pregnancy.
Animal and human study show fetal risk. |
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Schedule I
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Highly abused, illegal substance
controlled substance |
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Schedule II
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High potential for abuse. Controlled substance
Must use triplicate forms, No refills allowed. |
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Schedule III-IV
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Potential for abuse - Controlled substance.
Rx good for 6 months may be refilled up to 5 times Can be phoned in. |
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Schedule V
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Low potential for abuse - controlled substance
Rx Required in CA good for 6 months with up to 5 refills |
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Non controlled
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No abuse potential
Rx good for 1 year Unlimited refills Can be phoned in |
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PO
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Orally
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PV
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Per Vagina
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PR
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Per Rectum
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IV
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Intravenous
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IM
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Inter Muscular
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SQ
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sub cutaneous
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OS
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Left eye
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OL
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Left eye
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OD
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Right Eye
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OU
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Both Eyes
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AS
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Left ear
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al
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Left ear
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AD
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Right ear
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AU
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Both ears
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ac
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before meals
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agit
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shake
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am
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morning
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amt
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amount
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ante
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before
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ASA
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Asprin
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aq
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water
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bid
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twice daily
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bp
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blood pressure
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c
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with
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CBC
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complete blood count
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Ca
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calcium
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caps
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capsules
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CI
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chloride
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c/o
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complaint of
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D/C
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discontinue
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diag, Dx
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diagnosis
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dil
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dilute
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disch
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discharge
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dr
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dram
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et
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and
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Etoh
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alcohol
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exp
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expired
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FBS
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fasting blood sugarq
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Fe
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iron
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fl
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fluid
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gm
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gram
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gr
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grain
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gt
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drop
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gtt
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drops
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H, h, hr
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hour
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H2O
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water
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hs
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bed time
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Hx
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history
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K
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potassium
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liq
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liquid
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MDI
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meter dose inhaler
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Mg
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magnesium
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ms
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milligram
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MgSO4
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magnesium sulfate
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mm
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millimeter
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MOM
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Milk of Magnesia
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MS
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Morphine Sulfate
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Na
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Sodium
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NaCl
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Sodium Chloride
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neg
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negative
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NKA
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no known allergies
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NKDA
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no known Drug allergies
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NPO
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nothing per mouth (oral)
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oint
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ointment
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oz
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ounce
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PB
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phenobarbital
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pc
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after meals
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per
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by
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pm
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after noon
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PO
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orally
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prn
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as needed
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q
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every
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qd
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every day
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qhs
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at every bed time
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qid
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4 times a day
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qod
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every other day
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q6h
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every 6 hours
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qs
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quantity sufficient
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R/O
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rule out
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Rx
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prescription
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SL
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sublingual
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SOB
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shortness of breath
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sol
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solution
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ss
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one half
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stat
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immediately
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tabs
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tablets
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tbsp
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tablespoon (15ml)
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temp
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temperature
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tid
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three times a day
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tr, tinc
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tincture
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tsp
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teaspoon (5ml)
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ung
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ointment
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vag
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vaginal
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vol
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volume
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VS
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vital signs
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x
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times
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