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Enteral administration is less efficient due to first-pass metabolism.
Absorption is essential for drug effectiveness.
Inhalation provides rapid delivery to the lungs.
It is based on peak plasma concentration and dose.
Epinephrine is less affected by liver function.
It typically takes about 4-5 half-lives.
It pumps drugs out of cells to reduce absorption.
It is the fraction of the drug that reaches systemic circulation.
Drug-receptor complex formation triggers the response.
Protein and receptor phosphorylation mediate its action.
It suggests a wider margin of safety for the drug.
Continuous IV infusion maintains consistent drug levels.
Rectal administration targets the affected area directly.
Continuous IV infusion can lead to accumulation in liver impairment.
It takes about 3-4 half-lives for significant elimination.
An agonist activates the receptor to produce a response.
Gentamicin is effective against pan-sensitive E. coli.
It is calculated based on the ratio of effective to toxic doses.
CYP3A4 metabolizes a large number of drugs.
Smooth endoplasmic reticulum contains drug-metabolizing enzymes.
Acetaminophen glucuronidation is a metabolic process.
It resembles other opioid-related side effects.
12.5% remains after two half-lives.
Being a weak base with a pKa of 7 enhances permeability.
It ion traps the drug in urine to enhance elimination.
Glucuronidation remains effective despite aging.