DOH Pharmacist Exam study materials
DOH Pharmacist Exam study resources

DOH Pharmacist Exam flashcards

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32 cards. Read the term and the definition here. The deck at the top of this page is optional.

Bioisostere
A functional group with similar size, shape, and electronic properties to another, used to replace it in a molecule to preserve activity while improving metabolism or stability.
Lipinski Rule of Five
A set of criteria predicting oral drug-likeness: molecular weight below 500, LogP below 5, hydrogen bond donors below 5, and acceptors below 10.
Prodrug
An inactive compound that requires chemical or enzymatic conversion in the body to release the active drug, used to improve solubility, permeability, or stability.
Alkaloid
A nitrogen-containing, usually basic plant secondary metabolite such as morphine, quinine, or atropine, often with potent pharmacological activity.
Cardiac glycoside
A plant glycoside, such as digoxin from Digitalis, whose aglycone inhibits sodium-potassium ATPase, increasing intracellular calcium and cardiac contractility.
Tannin
A polyphenolic plant compound that binds and precipitates proteins, producing an astringent effect and serving as an antidote for alkaloid poisoning.
Volatile oil
A terpenoid or phenylpropanoid plant extract obtained by distillation, evaporating at room temperature and responsible for characteristic plant aromas.
Bioavailability
The fraction of an administered dose reaching systemic circulation unchanged, calculated from the ratio of test to intravenous AUC adjusted for dose.
HLB system
A numerical scale classifying surfactants by hydrophilic-lipophilic balance, where low values favor water-in-oil and high values favor oil-in-water emulsions.
Sterility assurance level
The probability that a single unit in a sterilized batch remains non-sterile, typically set at one in one million for terminal sterilization processes.
Suppository displacement value
The number of parts by weight of drug that displaces one part of base, used to calculate correct base quantity when preparing suppositories.
Therapeutic index
The ratio of the toxic dose to the effective dose for a drug; a low value indicates a narrow margin requiring therapeutic drug monitoring.
Competitive antagonist
A drug that binds reversibly at the same receptor site as the agonist, shifting the dose-response curve rightward and increasing EC50 without lowering maximal effect.
Type B adverse reaction
An unpredictable, idiosyncratic adverse drug reaction that is not dose-related, such as anaphylaxis or Stevens-Johnson syndrome.
N-acetylcysteine
The antidote for acetaminophen overdose, replenishing glutathione stores and detoxifying the reactive metabolite NAPQI in the liver.
HbA1c target
The glycated hemoglobin goal, generally below seven percent for most adults with diabetes, reflecting average blood glucose over about three months.
INR
The international normalized ratio, a standardized measure of prothrombin time used to monitor warfarin therapy, typically targeted between two and three.
Therapeutic drug monitoring
Measurement of plasma drug concentrations to individualize dosing for drugs with narrow therapeutic index and clear concentration-effect relationships.
Five rights of dispensing
A safety checklist confirming the right patient, drug, dose, route, and time before dispensing, reducing medication errors.
LASA drugs
Look-alike or sound-alike medications whose similar names or packaging risk selection errors, mitigated by tall-man lettering and separate storage.
Informed consent
A patient's voluntary agreement to treatment after receiving and understanding information about benefits, risks, and alternatives, reflecting the principle of autonomy.
Volume of distribution
The apparent volume relating the amount of drug in the body to its plasma concentration, indicating the extent of tissue distribution.
Half-life
The time required for plasma drug concentration to fall by half, calculated as 0.693 times volume of distribution divided by clearance.
Steady state
The condition where drug input equals elimination, reached after approximately four to five half-lives of constant dosing.
Loading dose
An initial larger dose calculated as volume of distribution times target concentration divided by bioavailability, used to reach therapeutic levels rapidly.
Bioequivalence
A regulatory determination that two products have comparable rate and extent of absorption, with the ninety percent confidence interval for AUC and Cmax within 80 to 125 percent.
ABC analysis
An inventory classification method that ranks items by annual usage value, focusing control efforts on the small number of high-value items.
Cost-effectiveness analysis
A pharmacoeconomic method comparing alternatives by cost per unit of clinical outcome, such as cost per life-year gained.
QALY
A quality-adjusted life-year, a utility measure combining survival duration with health-related quality of life, used in cost-utility analysis.
Herd immunity
Indirect protection of susceptible individuals when a sufficient proportion of a population is immune, reducing transmission of an infectious disease.
Pharmacoepidemiology
The study of drug use and effects in large populations using observational designs such as cohort and case-control studies to detect safety signals.
Primary prevention
Public health measures that prevent disease before it occurs, such as immunization, health education, and risk-factor modification.