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74 Cards in this Set

  • Front
  • Back

Drug-drug interactions

-can occur when taking 2 or more drugs


-can be desired and intended


-can be undesired and unintended

3 consequences of drug-drug interactions

1. Intensification of effects


2. Reduction of effects


3. Creation of unique response

4 basic mechanisms of drug-drug response

1. Direct chemical or physical interaction


2. Pharmacokinetic interaction


3. Pharmacodynamic interaction


4. Combined toxicity

Drug absorption effects in drug-drug interaction

-drug enhanced or reduced


-ex: laxities, elevating gastric pH

2 ways drug distribution can be altered

1. Competition of protein binding


2. Alteration of extracellular pH

Metabolism alteration or drug interaction

Inducing synthesis of hepatic drug-metabolizing enzymes

Inducer

When a drug metabolism is stimulated by increasing the synthesis of a hepatic drug metabolizing CYP enzymes

Substrate

A drug that is metabolized by an enzyme

Inhibitor

Drug that decreases the metabolism of other drugs by inhibiting the activity of the enzymes

4 effects that drugs that induce p-glycoprotein have on other drugs

PGP exports drugs from cellls


1. Reduced absorption


2. Reduced fetal drug exposure


3. Reduced brain drug exposure


4. Increased drug elimination

Desirable drug-drug interactions

- drugs that increase therapeutic effects


-drugs that reduce toxicity



-drugs tha

Serious drug interactions is proportional to?

-drugs that reduce therapeutic effects


-increases toxicity

Ways nurses minimize adverse drug-drug interactions

1. Decrease # of medications


2. Take through drug history


3. Adjust dosage when inducer of metabolism is added or deleted


4.adjust administer timing

Co-administration with food can cause

1. Decreased/increased absorption


2. Grapefruit juice affecting metabolism


3.increase toxicity


4.drug action impact


5. Timing of administration

When should you administer dose when it states to take ok an empty stomach?

2 hours after a meal or 1 hour before

Pharmacodynamics

The study of what drugs do to the body and how they do it

Difference between pharmacokinetics and pharmacodynamics

Pharmacokinetics is how drugs move through the body and pharmacodynamics is about the effect drugs have on the body

Dose-response relationship

As the dose increases, the response will increase

Maximal efficacy and where on the dose-response curve is it

The largest effect a drug can produce


Efficacy is noticed on the curve as the height of the dose-response curve

Receptors and examples of receptors

-Chemicals in body that most drugs interact with


-examples are hormones, neurotransmitters, and regulatory molecules

4 Types of receptor families

1. G-coupled receptor system


2. Ligand-gated ion channel


3. Cell membrane embedded enzyme


4. Transcription factor

Selective drug and selective receptor

-selectivity is the drug elicits response for which it is given


-selective drug compared to a selective receptor, the receptors are selective for specific drugs due to it being the only drug to fit in that receptor

Simple occupancy theory

The intensity of a response of a drug is proportional to the number of receptors occupied

Modified occupancy theory

The relationship between affinity and intrinsic activity


High affinity = high potency


Increase intrinsic activity = increased max efficacy

Affinity

Strength of the attraction between a drug and its receptor

Agonist

Activate receptor


Mimics endogenous chemicals


Have affinity and increased intrinsic activity

Partial agonist

Agonist with moderate intrinsic activity, only activity on a certain level


The max effect = less then full agonist

Antagonist

Prevent or decrease receptor activation


Have affinity but no intrinsic activity

Non competitive antagonist

Bind irreversibly

Competitive antagonist

Able to bind reversibly

Drug responses that do not need a receptor

-antacids


-antiseptics


-laxative


-chelating agents

What makes it impossible to know how exactly a patient will respond to a medication

Interpatient variability

ED50

Dose require to produce an effective or therapeutic response to 50% of the population

Therapeutic index

Measure of the safety of the drug

Larger therapeutic index

Safer

Smaller or narrow therapeutic index

Less safe

Adverse drug reaction

Any unintended effect that occurs at Norma drug doses

Mild adverse drug reactions

Drowsiness


Nausea


Itching


Rash

Severe adverse drug reaction

Respiratory distress


Neutropenia


Heaptocellular injury


Anaphylaxis


Hemorrhage

Side effect

Nearly unavoidable secondary drug effect produced at therapeutic doses whereas adverse effects can be avoided

Toxicity

Adverse drug reaction caused by excessive dosing but may also occur at normal dosing

Allergic reaction

Immune response


Determined by the degree of sensitivity rather then dosage

Are allergies common to drugs?

No

Idiosyncratic effect

Drug response from genetic predisposition

Paradoxical effect

The opposite of intended drug response

Iatrogenic disease

Disease produced by drugs (or physician)

Physical dependence

Develops after long term use or certain drugs

Abstinence syndrome

Can result after discontinuation of drug depended treatment after the body has adapted to drug exposure

Carcinogenic effect

Only a few drugs are carcinogenic



Cancer drugs have the most carcinogenic potential

Teratogenic effect

Drug-induced birth defects

2 types of organ specific toxicity

1. Hepatotoxic drugs- leading to liver failure


3. QT interval drugs- changes cardiac rhythm

Medication guides

Documents FDA approved to educate patient on minimizing harm from potentially harmful drugs

Black boxed warning

Strongest safety warning a drug can carry and still remain on the market

2 purposes of blacked box warning

1. Potentially severe side effects- fetal harm


2. Ways to prevent or reduce harm

REMS

Risk evaluation and mitigation strategy


Plan to minimize drug induced harm

Medication error

Major cause of morbidity and mortality

3 causes of fatal medication errors

1. Human factors


2. Communication mistakes


3. Drug name confusion

3 common human errors in drug therapy

1. Performance deficits- most common


2. Knowledge deficits


3. Miscalculation of dosage

Types of medication errors

Prescribing


Transcription


Dispensing


Administration

Factors that contribute to age related variations in drug response

1. Increase severity of illness


2.multiple pathologies


3. Treatment with multiple drugs

Affects of kidney disease on drug excretion

- reduced excretion and increased toxicity


-decrease dosage must happen

Liver disease and drug metabolism

-liver function decline, decreasing metabolism, and increasing drug levels

Electrolyte abnormalities and drug toxicity

When drugs are given thar decrease an electrolyte like potassium, while potassium levels are already low, this can cause fatal responses

Tolerance

Decrease responsiveness to drug after increased use


Requires higher doses

3 categories of drug tolerance

1. Pharmacodynamic tolerance-associated with long term administration of drugs


2. Metabolic tolerance-accelerated drug metabolism


3. Tachyphylaxis- reduced drug response due to repeated dosing

Placebo effect

Any response based on psychological reaction to drug

Are placebo effects beneficial

Not always and they can detract from the patients progress with them thinking the drug is harmful

Bioavailability

Ability of drug to reach the systemic circulation from its site of administration

What preparation would bioavailability likely occur in

Oral- due to tablet disintegration time, enteric coating, and sustained release formulas

Affect of diarrhea on drug absorption

Decreased drug absorption due to the diarrhea accelerating the drug through the intestine

Gender related drug differences

1. Women metabolize alcohol slower


2. Certain opioid analgesics are more effective in women


3. Quinidine cause greater QT interval in women

What effect can starvation have on drugs

Starvation can reduce the bonding of drugs

What interaction can drugs have on comorbities

Drugs taken to treat one condition may complicate management of another

Factors that influence patient to take medication

Manual dexterity


Visual acuity


Intellectual capacity


Physiologic state


Attitude toward drugs


Ability to pay