Module 2 study guide Flashcards
Idiosyncratic reaction
Adverse effects that are completely unexpected and not previously known to be associated with a particular medicine.
Involves abnormal susceptibility to a medication, possibly from genetic trait or dysfunction of a metabolic enzyme.
Medication biotransformation
Occurs in liver
Ability to cause biotransformation
Kidney, skin, lungs, GI tract
Four possible effects on body
Inactive substance can become active - Metabolite
Capable of producing desired or unwanted clinical effects
Inactive medication can be changed into another active medication- active metabolite
Active medication, may be completely or partially inactivated- inactive metabolite
Medication is transformed into a substance that is easier for the body to eliminate- inactive/ active metabolite
Steven johnson syndrome
Severe and possibly Fatal reaction that mimics a burn
May be caused by some antibiotics and anti seizure meds
Lipid soluble vs. water soluble
Lipid or fat soluble meds require higher weight based dose in older adults because of their higher body fat percentage and increased fat distribution
Water soluble requires higher weight based dose for infants because they have a higher percentage of body water
All but the larger lipid soluble medication can easier pass through cell Membranes
Acetylcholinesterase inhibition
Nerve agent toxicity which permits excessive release of ACH which leads to elevated levels in the body
Atropine is treatment
Synergism
Two meds with similar effects combined to produce an effect greater than the sum of the meds effects\
EX: fentanyl and versed acts as a chemical sedative
Potentiation
Definition: effect of one med is greatly enhanced by the presence of another med which does not produce the same effects
EX: promethazine is given to increase the effects of codeine or other antitussives for more improved relief of cough than is achieve by the antitussives alone.
Bioavailability
Definition: percentage of the unchanged med that reaches systemic circulation
Varies significantly from one med to another except when administered by IV
Meds by IV have 100% bioavailability
Irrelevant with meds that are sequestered such as activated charcoal
EX: the reduction in bioavailability due to first pass hepatic metabolism has already been taken into account with oral dosing explaining why the oral doses are significantly higher than IV doses given for the same purpose
Biotransformation
A process with four possible effects on a medication absorbed into the body: (1) an inactive substance can become active, capable of producing desired or unwanted clinical effects. (2) an active medication can be changed into another active medication. (3) an active medication may be completely or partially inactivated. (4) a medication is transformed into a substance (active or inactive) that is easier for the body to eliminate
Acetaminophen contraindications
Hypothermia either related to the toxic affects of the med
Environmental exposure
Known hypersensitivity
Severe active liver disease
Ace inhibitor side effects
Chronic dry cough, life threatening angioedema
Immune mediated medication response
Medications and substances present in the environment can trigger an exaggerated response from the body’s immune system, which is generally described as an allergic reaction. (medication sensitivity, anaphylaxis)
Alpha blocking medications
Alpha adrenergic receptor antagonists
Prevent endogenous catecholamines from reaching alpha receptors, primarily in smooth muscle of blood vessels
Lower BP (particulars diastolic)
Decrease systemic vascular resistance
Pts taking alpha blockers at home are susceptible to orthostatic hypotension and tachycardia.
Prescribed to pts with hypertension, enlarged prostate gland, glaucoma
Renal Failure
More susceptible to the adverse effect of medications than other patients. Renal Failure hinder the capability of the kidneys to eliminate medications properly. (last step in Pharmacokinetics)
Liver Failure
Patients with liver dysfunction are at risk of toxicity from oral medications, even at their conventional dose because the first pass effect is impaired in these individuals
A larger amount of the medication will reach their circulatory system
Alpha-1 Receptors
Adrenergic Receptor, Alpha-1 receptors primarily cause vasoconstriction
Alpha-2 Receptors
Adrenergic Receptor, Alpha-2 receptors generally cause smooth muscle contraction, inhibition of insulin release, induction of glucagon release, and suppression of further norepinephrine release
Lb to kg calculation
Lbs÷2.2 (on calculator)
Lbs÷2 then minus 10% (for freehand)