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what is generic name and what are the characteristics?
a common and standardized name derived from the more complex chemical name
not capitalized, is the name of all of that drugs regardless of the brand name (e.g., acetaminophen, cetirizine, diphenhydramine)
what is the brand name and what are the characteristics?
a trade name established by the producer of the medications
capitlized (acetaminophen → Tylenol, cetirizine → Zyrtec, diphenhydramide → Benadryl)
what is bioequivalent in term of pharmacology?
the principle that a generic medication would include the (1) same active ingredient and that the generic medication would have the (2) same rate and extent of absorption while producing the (3) same therapeutic effects as the brand name counterpart
what is pharmaceutical equivalent in term of pharmacology?
the prinnciple that a medication whether generic or brand name must (1) contain the same type and amount of active ingredients, (2) same dosage form (e.g., capsule, solid pill, syrup, etc), (3) same strength, and (4) same route of administration (e.g., enteral, parenteral, etc)
what is therapeutic equivalent in term of pharmacology?
basically pharmaceutical equivalent + bioequivalent
pharmaceutical equivalent = same type/amount of active ingredient, same form, same strength, and same route
bioequivalent = same active ingredients, same rate and extent of absorption, and same therapeutic effects
what is biosimilar in term of pharmacology?
a biological medicine highly similar to another already approved biological medicine (both are similar in structure)
differences between enteral and parenteral route of administration and what are some of the examples?
enteral - administration of medications that uses the gastrointestinal (GI) tract
→ oral
→ sublingual
→ buccal
→ rectal
→ feeding tube
parenteral - administration of medications that bypass the gastrointestinal tract - only reserved for the injection-based route of administration
→ intravenous (IV)
→ intramuscular (IM)
→ subcutaneous
→ intradermal
what are other route of administration that is not enteral or parenteral?
inhalation
topical
otic
ophthalmic
what does the acronym LADME stand for in pharmacology and a short description for each?
Liberation - the breakdown of the medications - drug is released from its dosage form
Absorption - process where a drug is transferred from site of entry to circulating fluid
Distribution - transport of drug through the entire body
Metabolism - process of body inactiviting drugs
Excretion - process of body eliminating the drugs from our system whether that be through excretion, pee, or internal metabolism.
what is half-life in term of pharmacology? what are some factors that impact half life
the time required for 50% of the medication to be eliminated from the body
factors impacting half life of medication
age
genetics
health conditions (kidney or liver disease can delay drug metabolism - heart failure can impact the drug distribution and
what are factors that can influence liberation?
whether or not if the medication have an enteric coating (does not dissolve in the stomach but rather in the intestine)
the route of administration (e.g., IV will allow for faster entry and breakdown of dosage form as it is administred directly in the bloodstream)
acidity of stomach (if given oral)
nutritional state (depending on the drug, a meal can increase, decrease, or have no effect, on the breakdown of the medication
motility of GI tract
what are some factors that can influence absorption?
hydration (dehydration can cause the medication to take longer to be absorbed)
body composition (e.g., fat mass) (a weightlifter body will take longer to absorp the medication compared to a frail old man)
metabolsim rate
blood flow
GI content/nutritional status
age
genetic
what are the factors that influence distribution of medication throughout the body?
blood flow
chemical properties
what is a therapeutic index?
a number range between the minimum effective concentration of a medication and the level where the medications would be toxic
what does it mean when a medication have a high therapeutic index?
when a medication have a high therapeutic index, the mediacation is lower risk and is generally safer as the range between the minium effectiveness and the toxicity level is large so there is less chance of making an error
what does it mean when a medication have a lw therapeutic infex?
the medication is higher risk because the range to which the concentration of the medication need to be for it to start working and the concentration to which the medication will become toxic is very narrow which would open less room for errors
what is an agonist medication?
a type of medications that activate a receptor in the body
what is an antagonist medication?
a type of medication that block a recaptor in the body
what is a partial agonist medication?
a medication that perform the function of both agonist and antagonist
a medication with a shorter half-life have a ___________ elimination
faster
what are some of the patient-specific factors that influence a medication’s half-life?
age
blood circulation
diet
hydration status
kidney function
liver function
obesity
gender
history of drug use
Presence of drugs that compete for binding sites or interact in other ways
genetic
for these type of questions - kind of critically think about how each factors might affects a medication’s half life and pick those answer
drug A has a half-life of 2 hours, if the initial plasma level of the drug is 1200 mg/L, what will its plasma level be after 8 hours?
75 mg/L
drug Z has a half-life of 8 hours, if the initial plasma level is 4800 mg/L, how many hours will it take for the plasma level to reach 180 mg/L?
about 40 hours
drug X has a half0life of 8 hours, if 800 mg is administered at 0100, hoq much of the drug would be eliminated after 24 hours?
700 mg of the drugs would be eliminated after 24 hours
true or false: increasing the amount of medication would slow down the onset of action for a medications
false; increasing the amount of medication can fastern the onset of action for the medication
what is peak action in term of pharmacology?
time of greatest amount of therapeutic effects
what is the duration of action in term of pharmacology?
how long did the medications last?
what is adverse reaction (ADR) in term of pharmacology?
a response to a drug that is noxious and unintended and which occurs at doses normally used in man for prophylaxis, diagnosis, or therapy of disease (e.g., itching, nausea, loss of appetite, weight loss, etc)
prophylaxis
action done to prevent the disease
what is an allergic reaction in term of pharmacology?
also known as hypersensitivity
reaction occur when patient is exposed to a drug, develops antibodies, and hen there is reexposed to drugs and has a reaction
what is the difference between adverse reaction (ADR) and allergic reaction?
adverse reaction (ADR) is symptoms that might occur due to intake of the medication but is usually not life-threatening and is unintended while allergic reaction is symptoms that occur due to the body’s hypersenstivity and can be life threatening
what is the additive effect in term of pharmacology?
using multiple medication with similar effects will increase the effect (the combined effect of two or more drugs acting together is exactly equal to the sum of their individual effects) (e.g., taking aspirin and acetaminophen together for added pain relief)
what is the synergistic effect in term of pharmacology?
using a medication and consuming something that would add onto the effect (e.g., taking a drowsy medication while also consuming alcohol)
what is the antagonistic effect in term of pharmacology?
taking a medication to counter the adverse effects of another medications (e.g., taking antiobiotic with birth control as antibiotic increase the likel