Adverse Effects Flashcards
what is a type A adverse drug reaction?
type A adverse drug reaction is an explainable/predictable adverse drug reaction
what is a type B adverse drug reaction?
unexplainable/idiosyncratic adverse drug reaction
what is a type C adverse drug reaction?
Chronic adverse drug reaction
what is a type D adverse drug reaction?
Delayed adverse drug reaction
which adverse drug reaction is most common?
Type A ADR’s account for approx. 80% of all reported ADR’s
name 4 examples of type A ADR’s
-
toxicity of overdose
- hepatic failure caused by high doses of acetaminophen
-
side effects
- sedation with the use of antihistamines
-
secondary effects
- development of diarrhea with antibiotic therapy
-
drug interaction
- theophylline toxicity in the presence of erythromycin therapy
describe the following example of type B ADR’s
- intolerance
- hypersensitivity
- pseudoallergic
- idiosyncratic
intolerance
- patients that are intolerant to certain drugs cannot be predicted; a number of patients are intolerant to aspirin and can experience tinnitus if they take the drug
describe the following example of type B ADR’s
- intolerance
- hypersensitivity
- pseudoallergic
- idiosyncratic
hypersensitivity
- anaphylaxis with penicillin administration; hypersensitivity is not dose-dependent or predictable through knowledge of the mechanism of action of the drug
describe the following example of type B ADR’s
- intolerance
- hypersensitivity
- pseudoallergic
- idiosyncratic
pseudoallergic
- radiocontrast dye reaction; pseudoallergic reactions occur on first exposure to a drug/agent in patients that are sensitive
- they do not need prior exposure as with type 1 hypersensitivity
describe the following example of type C ADR’s
- dependence
- chronic use
dependence
- some drugs such as benzodiazepines and B-blockers are known to induce physiological dependence if used chronically
describe the following example of type C ADR’s
- dependence
- chronic use
chronic use
some adverse effects only appear if drugs are used for months/years, e.g. steroids are associated with a risk of osteoporosis only if they are used chronically
type D ADR’s are delayed adverse effects that are normally ___ and ___ in nature; they are very rare and most commonly associated with the use of ____
type D ADR’s are delayed adverse effects that are normally carcinogenic and teratogenic in nature; they are very rare and most commonly associated with the use of chemotherapeutic agents
describe an on-target effect
exaggeration of the desired pharmacologic action of a drug
the increase in biological response in on-target effects can occur by which 3 mechanisms?
- deliberate of accidental dosing error
- alterations in the pharmacokinetics of the drug (e.g. decrease in liver of kidney function)
- alterations in the pharmacodynamics of the drug-receptor interaction (e.g. an increase in receptor number occurring during treatment)