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64 Cards in this Set
- Front
- Back
- 3rd side (hint)
Effects of a drug depends on what? |
dosage |
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Patients commonly think what is related to strength? |
numerical dosage |
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dosage: qD |
quaque die – one a day |
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dosage: BID |
bis in die – twice a day |
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dosage: TID |
ter in die – three time a day |
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dosage: q#h |
– Quaque # hours – once every # hours |
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What are risks with patients self-administration meds? |
- taking when symptomatic - taking too much / too little - giving to friends - selling |
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What questions to ask before prescribing medication? |
- What dose will be effective? - What does will cause harm? - How is medication absorbed/eliminated? - How quickly does medication take effect? |
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Researchers typically test the effect of drug on ___ before moving onto human |
animals |
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ED50 stands for ___ ___ ___; Represents the specific dose of a given drug that is effective in 50% of the population |
effective dose value |
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Different medications will have different ___ |
ED50 |
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How is ED50 helpful? |
- Used to compare different medications and determine if a drug is more potent than another.- It can also help determine which drugs have a wider therapeutic range |
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___: refers to the amount of a drug that produces a certain level of therapeutic effect |
Potency |
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Drug X reaches its ED50 at 2.0 mg, when compared with Drug Y, which reaches its ED50 at 8.0 mg. This suggests that Drug X is ___ than Drug Y. |
stronger; more potent |
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___ – Maximal effect a drug can produce regardless of the dosage prescribed |
Efficacy |
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Taking more than approximately 3.0 mg of Drug X or 10.0 mg of Drug Y will not increase the drug’s effectiveness, as these or higher doses may place the individual at risk for experiencing adverse side effects, toxic doses, or even overdose. this is an example of ___? |
Efficacy |
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potency and efficacy |
review |
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x and y axis; closer to the left is more ___; closer to the sky, more ___ |
potent; efficacy |
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Drug ___ – with each subsequent dose of a medication a patient experiences INCREASED effective treatment outcomes without change medication dosage |
sensitization |
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Drug ___ – with each subsequent dose of a medication a patient experiences a REDUCTION in treatment outcome without change in dosage |
tolerance |
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___ (acronym) – dose at which a drug will cause a toxic effect in 50% of the population |
Toxic Dose – TD50 |
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It is important to know the relative difference between the average therapeutic dose and the average toxic dose. This is defined as the ___. |
Therapeutic Index (TI) |
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How is TI calculated?The smaller the TI the ___ the risk |
TI = TD50/ED50; higher |
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Drug safety lethality: For Drug Y the ED50 is 8mg and the TD50 is 10mgThe TI of Drug Y is 10/8 = 1.25This is a very small TI and thus Drug Y may be ___ to administer. |
risky; since it has less room for therapeutic improvement and may have more of a chance to produce a toxic or adverse drug effect with increases in dosage |
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___ refers to how a substance travels through the body and brain by absorption, distribution, metabolism, and elimination. |
Pharmacokinetics |
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Pharmacokinetics focuses on how the body ___ a drug |
effects |
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___ of drug administration can effect the speed in which it is absorbed and distributed |
route |
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___ - swallowing |
Oral |
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___ – dissolving under the tongue |
sublingual |
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___ – absorbing though the membranes of the nasal or oral cavities |
Nasal/mucosal membrane |
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___ = breathing into the lungs |
inhalation |
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___ - through the skin |
transdermal |
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___ - injection under the skin |
subcutaneous |
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___ - through the rectum |
intra-rectal |
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___ - injection into the skeletal muscle |
intramuscular |
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___ - jection into a major vein |
intravenous |
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4 ways drugs cross membranes? |
Passive diffusionFacilitated diffusionActive transportEndocytosis |
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___- proportion of a drug that enters circulation |
bioavailability |
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Unless a drug is given IV the bioavailability will always be less than ___%; Medications will be metabolized and some portion of it will be ___ before reaching circulation |
100; eliminated |
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___ is the movement of a drug throughout the body. |
distribution |
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5 factors that affect distribution? |
Lipophilicity Blood flow Capillary permeability Plasma and tissue binding Volume of distribution |
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___; - the more lipophilic the easier it passes through membranes___ some organs have more blood flow than others, areas with more blood flow will have a higher distribution of the substance (brain is more than skin)___ ___ - how leaky a capillary is, different organs are different (liver is more than brain) ___ and ___ binding- some drugs will bind to certain tissues more than others. Also some will bind to Albumin which is found in plasma, this will slow down distribution.___ -- ___- theoretical volume that drug needs to occupy to create a certain concentration in the plasma. |
LipophilicityBlood flowCapillary permeabilityPlasma and tissue bindingVolume of distribution |
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____ describes the process by which a drug is altered chemically in the body into its metabolite, which may be more or less active. |
Metabolism |
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Where does metabolism occur? |
Liver |
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How many step process for metabolism? |
2 step |
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Phase 1 of metabolism makes the drug chemical more ___. This is accomplished mostly by using the ___ ___ system. |
reactive; Cytohrome P450 |
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The cytochrome P450 system is important because other medications can ___ or ___ this system. |
speed; slow |
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Metabolism: Phase 2- The 'activated' drug molecule is combined with another molecule to produce an ___ compound which is usually more water soluble making it easier for ___. |
inactive; excretion |
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___ is the process by which a drug or its metabolite is removed from the body. |
Elimination |
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4 places elimination can occur? |
This usually occurs in the kidneys (urine) but it can also take place through the gastrointestinal tract (feces) , the skin (sweat) or lungs (exhaled air). |
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____- amount of time it takes to decrease plasma concentration of a drug by half |
Half Life (t1/2) |
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Half-life tells us about the ___ of action of a drug |
duration |
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How many half-lives to eliminate a drug completely? |
4 to 5 |
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Taking a 100 mg dose of an oral medication with a half-life of 15 minutes, the following is true:15 minutes after the drug administration, ___ of the drug remains in the body. (__% eliminated)30 minutes after the drug administration, __ mg of the drug remains in the body. (__% eliminated)45 minutes after the drug administration, __ mg of the drug remains in the body. (__% eliminated)1 hour after the drug administration, __ mg of the drug remains in the body. (__% eliminated)
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50; 50% / 25; 75% / 12.5; 87.5% / 6.25; / 93.75% |
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Elimination: When drug doses are repeatedly administered the drug will accumulate in the body until it reaches a point where the rate of administration is equal to the rate of elimination. This is called ___ ___. |
Steady State |
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How long to reach steady state? This is important because when prescribing a drug you want the plasma concentration to be effective and not toxic. You want the steady state of the drug to be in therapeutic range. |
4 - 5 half-lives. |
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___ is defined as the study of the time course and intensity of the pharmacological effects of drugs |
Pharmacodynamics |
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Pharmacodynamics focuses on how a drug ___ the body |
affects |
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effects of pharmacodynamics are dependent on the ___ and ___ of exposure |
dose; route |
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What three individual factors affect response to drug therapy? |
Genetics; Age; Gender |
Genetics: People metabolize drugs differently based on their P450 enzymesAgeChildren: Still undergoing brain development, neural network connectivity and maturation. Weight less and are rapid metabolizers of substances, will therefore need smaller doses to avoid adverse effectsGeriatric: Physiological changes due to age as well as medical problems may lead to issues with the liver being able to metabolize drugs or the kidney being able to eliminate certain drugs. The heart may be too weak to circulate certain drugs to reach their target.Gender: Differences between men and women in regards to development, puberty, body composition all effect metabolism of drugs. Pregnancy has effect on this as well, and when women become pregnant. |
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3 types of drug interactions? |
Canceling effectsSynergistic effectsParadoxical effects |
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Drug-interactions that can happen w/ non-drug materials? |
Grapefruit juice; alcohol; herbal supplements |
Grapefruit Juice: Mixing some heart medications with grapefruit juice may alter effectiveness of the medication ( interferes with metabolism)Herbal Supplements: Mixing St. John's Wort with SSRI medication can lead to Serotonin Syndrome which can be life threatening (additive effects of 2 drugs)Alcohol:19% of the population takes prescription drugs that interact with alcohol WHILE also drinking alcohol. Effects differ based on drug but can lead to organ failure |
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Patients may also be ___ to specific substances within the drug such as excipients (the other stabilizing, bulking, or filling agents within a drug) |
allergic; |
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Drug interactions: This can be problematic as it can lead to patients or health professionals misinterpreting an excipient's ___ effect to that of the prescribed medication |
adverse |
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