Module 1 Flashcards
Who has full prescriptive Authority?
MD or DO a.k.a. physicians
What is prescriptive authority?
The legal right to prescribe drugs
What are the two components of prescriptive authority?
Right to prescribe independently and right to prescribe without limitation
What scheduled drug classes can PAs prescribe to?
Scheduled II-V
In Texas, APRNs can prescribe what scheduled class of meds?
Scheduled III—V
What are controlled substances?
Meds that require a prescription and not at risk for addiction
What are scheduled drugs?
Drugs that are at risk for addiction
Legend or controlled drugs are good for how much time from the date of the prescription?
How good are they after they have been turned into the pharmacy?
From the date the prescription is written it is good for one month.
From the date the prescription is written and has been turned into the pharmacy, it is good for one year from the date it was written
Controlled drugs in class three through five are good for how long?
It is good for six months from the date it was written
But if not turned into the pharmacy, it will expire in 1 month.
Class II schedule drugs Are good for how long from the date of it being issued?
It is good for seven days from the date it was issued
What are the three primary reasons for a drug monitoring?
To determine therapeutic dosage, Evaluating medication adequacy, and identifying adverse effects
What are the four Processes of pharmacokinetics?
Absorption, distribution, metabolism, excretion
What is pharmacokinetics?
The study of drug movement throughout the body
What is absorption?
The drugs movement from that site of administration to the blood
What is distribution?
The drugs movement from the blood to the interstitial space of tissues and into cells
What is another name for metabolism?
Bio transformation
PGlycoprotein or PGP Is what?
It is a multi drug transporter proteins that transports a wide variety of drugs out of cells
For a drug to directly penetrate a Membrane what kind of solubility would it need to be?
Direct penetration of the membrane is most common
A drug must be lipid soluble or lipophilic
Can polar molecules and ions Dissolve in lipids?
No
Only non-ionized and non-polar can dissolve in liquids
The ionization of the drug is?
PH dependent
What is PH portioning also called ion trapping?
The process where a drug accumulates on the side of a membrane were the pH most favors it’s ionization
Which side do acidic drugs accumulate on?
Acidic side or alkaline side
Alkaline side
Basic drugs tend to accumulate on which side?
Acidic or alkaline
Acidic side
The rate of absorption determines what?
How soon effects will begin
The amount of absorption helps determine what?
How intense effects will be
The rate of dissolution helps determines what?
The rate of absorption
In regards to absorption, when the surface area is larger, the absorption is what?
Faster
When the surface areas larger, the absorption is faster
In regards to absorption, the greater the concentration gradient has, will have what effect on absorption?
Absorption will be faster
Which drugs are absorbed faster: High lipid soluble drugs or low lipid soluble drugs?
High lipid soluble drugs
What is distribution?
Movement of drugs from systemic circulation or blood to the side of drug action
Name 3 factors determine distribution
Blood flow to the tissues, ability of the drug to exit the vascular system, Ability of the drug to enter cells
In regards to distribution, and exiting the vascular system drugs usually leave the blood how?
Drugs in the vascular system leave the blood at capillary beds
In regards to the blood brain barrier why are neonates at risk?
The blood brain barrier has tight junctions that prevent drug passages, this is not Fully developed At birth
How do you most drugs cross the placenta?
Most drugs possible center via simple diffusion
Drugs that are non-ionized and non-polar can do you what?
Pass through membranes more easily Because they are more lipid soluble friendly
Does IV Have any barriers to absorption?
No, there is no barriers to absorption
In regards to protein binding,
Are drugs needing to be bound or free to be pharmacologically active?
Drugs need to be unbound or free to be pharmacologically active
Most drug metabolism that takes place in the liver is performed by hepatic microsomal enzyme system known as what?
The P450 system also know as cytochrome P450
Most drug metabolism occurs where?
Takes place in the liver
P4 50 enzymes can be inhibited Or induced by drugs,Leading to what?
To the development of drug to drug interactions which can result in an adverse drug reactions and therapeutic failures
A drug that induces the P4 50 enzyme can affect another drugs rate of metabolism and its effectiveness in what way?
It can increase another drug’s rate of metabolism which decreases it concentration and reduces effectiveness
This requires increase dosage and can cause therapeutic failure
A drug that inhibits the P4 50 enzyme can affect the rate of metabolism and its effectiveness how?
A inhibiting drug can decrease another drugs rate of metabolism and prolong its effects.
This will require decreased Dosages and may lead to toxic drug levels
What is a pro drug?
Is a compound that is pharmacologically in active when administered but once Undergoing metabolism it becomes active
The liver does not develop its full capacity to metabolize drugs until how long after birth?
Until approximately one year after birth
Drugs that increase the rate of drug metabolism Are called what?
Inducers
Drugs that decrease the rate of metabolism are called what?
Inhibitors
What is the first pass effect?
The rapid inactivation of certain oral drugs Because they are Carrie directly to the liver before they enter systemic circulation
What is enterohepatic recirculation?
It is a repeating cycle and went to drug is transport deliver to the intestate and then back to the liver
Drugs can remain in the body much longer than they otherwise would
Name six methods drugs can exit their body through
Urine Bile Sweat Saliva Breast milk Expired air
What are the three processes for excretion or elimination?
Glomerular filtration, passive tubular reabsorption, active tubular secretion
Can drugs that are polar, ionized, or a protein bound enter the breastmilk?
No
Only lipid soluble drugs have ready access to breastmilk
What is the minimum effective concentration (MEC)?
It is the plasma level less than which therapeutic effects will not occur
(Aka a drug must be present in concentrations at or greater than MEC)
What is toxic concentration?
The plasma level at which toxic effects begin
Drugs are having a narrow therapeutic range Should:
Be monitored for signs and symptoms of toxicity
What is a Drugs half-life defined as?
As the time required for the amount of the drug in the body to decrease by 50%
When a drug is administered repealing in the same dose, plateau will be reaching approximately how many half lives?
4-5 half lives
What is pharmacodynamics?
It is the study of a drug’s action on the body and how the drug produces it’s therapeutic effects
What is maximal efficacy? In relation to pharmacodynamics and that dose- response relationship
It is the largest effect that a drug can produce
What is relative potency?
Potency refers to the amount of drug we must give to elicit an effect
What is affinity?
It refers to the strength of the attraction between a drug and its receptor
Drugs with strong and high in affinity are…
Attracted to their receptors
Drugs with high affinity are effective in low doses and more potent
What is intrinsic activity?
It refers to the ability of a drug to activate the receptor after binding
Low intrinsic—low maximal efficacy
High intrinsic—maximal efficacy
Affinity an intrinsic activity are related to what pharmacodynamic theory?
Modified occupancy theory
What is an agonist?
A drug that mimics the body’s own regulatory molecule responses
Agonists=activate
Affinity allows binding and intrinsic activity allows the bound agonist to activate or turn on receptor function
Drugs a block the actions of an endogenous regulators are called what?
Antagonist
What are drugs that mimic the actions of endogenous regulatory molecules but they produce responses of intermediate intensity?
Partial Agonists
How do antagonist work?
They prevent receptor Activation by endogenous regulatory molecules and drugs
In regards to affinity And intrinsic activity, antagonists have what?
They have affinity for a receptor but No intrinsic activity
Affinity allows binding to a receptor but lack of intrinsic activity prevents receptor activation
In regards to affinity and intrinsic activity, Agonists have what?
Intrinsic activity Is high and affinity is high
What is the difference between non-competitive and competitive antagonist?
Non-competitive antagonists bind irreversibly
Competitive Antagonist bind reversibly to receptors
NI-non competitive irreversible
CR—competitive reversible
When continuously exposed to an agonist a cell can become…
Desensitized
Continuous exposure to antagonists causes the cell to become…
Hyper sensitive
What is ED 50?
It is defined as the average effective dose required to produce a therapeutic response in about half of the population
Can be considered the standard dose
What is LD50?
The average lethal dose in 50% of the population
Is a drug safe or unsafe if it has a large or wide therapeutic index
Relatively unsafe
Grapefruit juice raise his drug levels by inhibiting the CYP3A4 metabolism enzyme in which some meds will need to be changed how?
Dosage will need to be decreased
Grapefruit juice increases the drug levels
What are adverse drug reactions?
World health organization defines it as any noxious unintended and undesired effect that occurs at normal drug doses
What is a side effect?
Nearly unavoidable secondary drug affects produce a therapeutic doses
These are predictable, intensity is dose dependent
What is toxicity?
It is defined as the degree of detrimental physiological effects caused by excessive drug dosing
What is an allergic reaction?
An allergic reaction is an immune response
For an allergic reaction to occur, we exposure to a drug can trigger the response. There must be a prior sensitization of the immune system
What is an idiosyncratic effect?
An uncommon drug response resulting from a genetic predisposition
What is a paradoxical effect?
This is the opposite of the intended drug response
What is an Iatrogenic disease?
It is a disease that occurs as a result of medical care treatment with drugs
A.k.a. Drugs promote this disease
What is the QT interval?
It is the measure of time required for the ventricles to repolarize (relax) after contraction
When a QT interval is prolonged patients can develop what 2 heart rhythms?
They can develop torsades and Ventricular fibrillation
When is a med guide required?
The FDA makes it a requirement, when they determine that patient adherence to the directions for drug use is essential for efficacy and what they need to know about serious side effects
Created to minimize germ from potentially dangerous drugs
What is a black box warning?
It is the strongest safety warning still stay on the market
FDA requires this when serious or life-threatening risks related to the drug—this will alert providers for severe side effects
What is tolerance?
It is defined as a decrease responsiveness to a drug as a result of repeated drug administration
Will usually require higher doses
What is a reduction in a drug’s Responsiveness brought on by repeated dosing over a short time?
This can take days or longer to develop
Tachyphylaxis
What is bioavailability?
It refers to the amount of an active drug that reaches the systemic circulation (blood) from its site of admin
Think sustained release, enteric coating, extended or delayed release
Usually involves oral meds
What is precision medicine? And what is it related to?
Precision medicine refers to a more general approach to find it effective strategies for treatment of similar group of patients with specific genetic, lifestyle, and environmental factors
Pharmacogenomics
In the third trimester pregnancy Reno blood flow is doubled causing a large increase in the glomerular filtration rate what impact can this mean for a patient who is pregnant and taking medications?
Dosages of drugs may need to be increased due to the increase of drug elimination through the kidneys
This can also occur in the liver
For women who are pregnant tone and motility of the bowel are decreased which can have what effect on medications?
More time for drugs to be absorbed so a reduction in dosage might be needed
This goes for drugs that undergo enterohepatic recirculation
What are symptoms of a drug dependent infant?
Shrill cry, vomiting, and extremely irritability