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188 Cards in this Set

  • Front
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A,D,M,E

Stands for what in Pharmokinetics?
Absorption

Distribution

Metabolism

Excretion
Define Pharmokinetics
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.
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
Define Absorption
Transfer of drug from its site of administration to the blood stream.
Define Pharmacodynamics
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.
Define Metabolism
Process by which the body chemically alters drugs through enzymatic action. (biotransformation)
Define Distribution
Process by which a drug reversibly leaves the blood stream and enter the intestitum. (extracellular fluid)
Define Ionized
Charged

Has + or -

ig: K+
Define Unionized
Not Charged

No + or -

ig: K
Define Pharmacology
Science concerning with drugs, their sources, appearances, chemistry action and uses.
Define
Pharmacodynamics
The study of the physiological effects of drugs and the mechanism of their action on the body.
Define
Therapeutic Dose
The amount of medication required to produce the desired effect.
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.
Define
Maximum Effective Dose
Largest dose which is able to give with safety
Define
Minimum Effective Dose
The smallest dose that will produce an appreciable effect.
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.
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.
What is the chemical nature of a drug?
Lipid Soluble
or
Water Soluble
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.
What is the mode of transportation across a membrane?
Lipid soluble drugs needs Lipid Transporter at the blood level. It can't dissolve in water.
Lipid Soluble drugs need?
Lipid transporter
Water Soluble drugs can be dissolved in?
Blood
Are water soluble drugs safer drugs?
Yes
Define
Unbound Drugs
Pharmacology ACTIVE drug that can cross the membrane. The drug is not bound to to a carrier proven or molecule.
Define
Therapeutic Index
Ratio of toxic dose to the effective dose.

(TI) = Toxic dose / Effective Dose

You look for a Narrow Therapeutic Index
Lipid Soluble drugs need what to work?..
Lipid Transporters
Are Lipid Soluble drugs More Toxic to the body?
YES
Can Lipid Soluble drugs dissolve in blood?
NO

But they can pass through the cell membrane.
Acidic Drugs are?
Ionized
Alkaline Drugs are?
NOT Ionized
Define
Efficacy
Measure of how well a drug produces a response.
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.
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.
Define
Agonist
A drug is called agonist when binding to the rector results in a response.
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
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
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
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.
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.
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.
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.
Define
Biotransformation
Metabolic conversion of drug molecules to more water-soluble metabolites that are more deadly excreated.
Phase 1 Biotransformation
Modification of the drug molecule via oxidation, reduction or hydrolysis.
Phase 2 Biotransformation
Conjugation with endogenous compounds via the activity of transferases
Define
Absorption
Process of entry of a drug into the systemic circulation from the site of administration.
Define
Bioavailability
Measure of the fraction of an administered dose that reaches the systemic circulation.

Ie: Intravascular doses have 100% bioavaliability.
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.
Define
Distribution
Process of distribution of a drug from the systemic circulation to organs and tissue.
What are the 2 types of special barriers?
Blood Brain

Placental
Nonionized drugs have what charge?
Uncharged form
Ionized druge have what charge?
Have a positive and negitive charge.
What modes of drug transport are there?
Passive Diffusion - Down Gradient

Facilitated Diffusion - Down Gradient

Active Transport - Against Gradient
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.
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.
Drug permeation is dependent on?
Solubility

Concentration Gradient

Surface area vascularity
Water Soluble drugs are?
Ionized Drugs
Lipid Soluble Drugs are?
Nonionized Drugs
Unbound drugs are?
Active Drugs or compounds that are NOT bound to a carrier protein - Pharmacolgically Active.
Active Drugs are considered what type of drugs?
Unbound
Define
Passive Diffusion
Movement of material from an area of high concentration to and area with lower concentration.

*It does not require Active Transport.
Define
Solubility
Ability to diffuse through lipid bilayers (Lipid Solubility)

*Important for most drugs- however water solubility can influence permeation through aqueous phase.
Define
Tolerance
process of adapting to a drug over a period of time and subsequently require higher doses to achieve the same effect.
Normal PH is?q
7.0
Base or Alkalinity is levels
8-10 PH
Acidity PH levels are
6-0 PH
Define
therapeutic Index
Therapeutic agent that causes the therapeutic effect to the amount that causes death or toxicity.
Define
Narrow Therapeutic Index
Small changes in the dosage could cause toxic effects
Define
Bioavailability
The fraction of administered drug that reaches the systemic circulation
Define
Half-Life
(t1/2) The time required for the concentration of a drug to drop by 50%.
Define
Steady State
When the plasma concentration of a drug remains constant, the rate of elimination = rate of input.
Define
Efficacy
the maximal RESPONSE produced by a drug
Define
Potency
?how much drug is required to elicit a given response )increase potency=Decrease dose)
Define
Agonist
An agent that can bind to a receptor and elicit a response.
Define
Partial-Agonsit
An agent that block the binding site and causes less response than a true agonist.
Define
Antagonist
Interacts with receptor by produces no action of its own. It blocks the action of agonist.
Define
Therapeutic Index
The ration of toxic dose to the effective dose.

TI = Toxic dose/effective dose
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.
Superscription
Contains the symbol Rx, meaning "take throu" or "recipe"
Inscription
Specifies the name and strength of the dug
Signature or Sig
Gives the directions for taking the medication and route of administration
Subscription
Gives directions to the pharmacist. It designates the # of doses, the quantity to be dispensed and the form of the drug.
What should be included on all prescriptions?
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
Pregnancy Category A
Controlled studies show no risk.

No risk to fetus
Pregnancy Category B
No evidence of rush in humans.

animal findings show risk but humans show no risk
Pregnancy Category C
Risk cannot be ruled out.

Human studies lacking, animal studies show positive for fetal risk.

Potential benefits may justify risk
Pregnancy Category D
Postive evidence of risk.

proof of risk to fetus.May be acceptable in life threatening situations.
Pregnancy Category X
Contradicted in pregnancy.

Animal and human study show fetal risk.
Schedule I
Highly abused, illegal substance

controlled substance
Schedule II
High potential for abuse. Controlled substance

Must use triplicate forms, No refills allowed.
Schedule III-IV
Potential for abuse - Controlled substance.

Rx good for 6 months
may be refilled up to 5 times
Can be phoned in.
Schedule V
Low potential for abuse - controlled substance

Rx Required in CA
good for 6 months with up to 5 refills
Non controlled
No abuse potential

Rx good for 1 year
Unlimited refills
Can be phoned in
PO
Orally
PV
Per Vagina
PR
Per Rectum
IV
Intravenous
IM
Inter Muscular
SQ
sub cutaneous
OS
Left eye
OL
Left eye
OD
Right Eye
OU
Both Eyes
AS
Left ear
al
Left ear
AD
Right ear
AU
Both ears
ac
before meals
agit
shake
am
morning
amt
amount
ante
before
ASA
Asprin
aq
water
bid
twice daily
bp
blood pressure
c
with
CBC
complete blood count
Ca
calcium
caps
capsules
CI
chloride
c/o
complaint of
D/C
discontinue
diag, Dx
diagnosis
dil
dilute
disch
discharge
dr
dram
et
and
Etoh
alcohol
exp
expired
FBS
fasting blood sugarq
Fe
iron
fl
fluid
gm
gram
gr
grain
gt
drop
gtt
drops
H, h, hr
hour
H2O
water
hs
bed time
Hx
history
K
potassium
liq
liquid
MDI
meter dose inhaler
Mg
magnesium
ms
milligram
MgSO4
magnesium sulfate
mm
millimeter
MOM
Milk of Magnesia
MS
Morphine Sulfate
Na
Sodium
NaCl
Sodium Chloride
neg
negative
NKA
no known allergies
NKDA
no known Drug allergies
NPO
nothing per mouth (oral)
oint
ointment
oz
ounce
PB
phenobarbital
pc
after meals
per
by
pm
after noon
PO
orally
prn
as needed
q
every
qd
every day
qhs
at every bed time
qid
4 times a day
qod
every other day
q6h
every 6 hours
qs
quantity sufficient
R/O
rule out
Rx
prescription
SL
sublingual
SOB
shortness of breath
sol
solution
ss
one half
stat
immediately
tabs
tablets
tbsp
tablespoon (15ml)
temp
temperature
tid
three times a day
tr, tinc
tincture
tsp
teaspoon (5ml)
ung
ointment
vag
vaginal
vol
volume
VS
vital signs
x
times