Complete Review for the Pharmacy Technician: Drug Classifications and Formulations

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Vocabulary flashcards covering human anatomy, organ systems, pathophysiology, pharmacokinetics, pharmacodynamics, dosage forms, and core pharmacological principles from Chapter 1 of Complete Review for the Pharmacy Technician (4th Edition).

Last updated 6:29 PM on 10/18/26
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35 Terms

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Pharmacotherapy

The use of medications to treat human disease.

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Physiology

The study of human normal body function and the ways in which the body and its organ systems work.

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Pathophysiology

The study of what goes wrong and the disrupted physiologic processes in diseases.

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Homeostasis

A balanced state in which the body functions normally, organs work in concert, nutrients and oxygen are distributed, and metabolic wastes are processed and eliminated.

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Atomic Number

The number of positively charged protons located in the nucleus of an atom.

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Atomic Mass Number

The total sum of protons and neutrons present in the nucleus of an atom.

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Afferent Nerves

Nerves that gather sensory information from in and around the body and transmit it toward the brain.

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Efferent Nerves

Nerves that carry instructions and regulatory signals from the brain back to muscles, glands, and organs.

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Sebum

An oily substance secreted by sebaceous glands connected to hair follicles that prevents the skin and hair from drying out.

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Signs (of Disease)

Subjective clues describing how a patient experiences and characterizes their illness.

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Symptoms (of Disease)

Objective clues discovered by healthcare professionals during physical examination, laboratory testing, or diagnostic procedures.

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Epidemiology

The study and analysis of health patterns, causes of disease, and therapeutic outcomes across populations of people rather than individuals.

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Pharmacogenomics

The study of how an individual's genetic variations influence their response to medications and risk of disease.

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Pharmacokinetics

The study of the movement of drugs through the body, comprising absorption, distribution, metabolism, and excretion (ADME).

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Disintegration

The process in which a solid oral dosage form, such as a tablet, breaks apart into small particles within gastrointestinal fluids.

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Dissolution

The process by which drug particles dissolve into gastrointestinal fluids, allowing the drug to become available for absorption into the blood.

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Bioavailability

The ratio or percentage of an administered drug dose that successfully reaches the systemic circulation via the bloodstream.

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First-Pass Metabolism

The extensive breakdown and transformation of an orally administered drug in the liver before it ever reaches the systemic circulation, which decreases its oral bioavailability.

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Prodrug

An inactive chemical agent that requires metabolic conversion by the body into an active, therapeutic drug.

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Volume of Distribution

A mathematical parameter describing the extent to which a drug disperses out of the blood and into various bodily compartments and tissues.

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Clearance

The mathematical expression of the amount of drug eliminated or metabolized to inactive compounds by an organ or tissue over a given duration of time.

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Half-Life

The time required for the concentration of a drug in the serum to decrease by one-half (50%50\%).

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Pharmacodynamics

The study of what drugs do in the body and the relationship between serum or tissue drug levels and their pharmacological effects.

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Narrow Therapeutic Range

A narrow margin between a medication's therapeutic dose and toxic dose, where small variations in blood concentration can produce toxicity or therapeutic failure.

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Suspension

A liquid dosage form containing finely divided, insoluble drug particles dispersed throughout a vehicle that must be shaken thoroughly before measuring each dose.

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Elixir

A clear, sweetened oral liquid preparation that contains alcohol and is used to dissolve medications and mask unpleasant, bitter tastes.

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Suppository

A solid dosage form that remains solid at room or refrigeration temperatures but melts or dissolves when inserted into a body cavity such as the rectum, vagina, or urethra.

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Depot Injection

An intramuscular injectable suspension formulated to release medication slowly and continuously into the bloodstream over an extended duration, such as 33 to 4 weeks4\text{ weeks}.

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Generic Name

The standardized nonproprietary name assigned to an active drug ingredient by the United States Adopted Names (USAN) program.

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Brand Name

The proprietary or trade name designated to a pharmaceutical product by the manufacturer that first developed or marketed it.

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Off-Label Use

The clinical use of an FDA-approved drug for an unapproved indication that is not listed in the official manufacturer labeling.

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Adverse Effects

Unintended secondary effects (side effects) that occur when a drug is administered at normal, recommended doses.

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Contraindication

A specific disease, condition, or patient characteristic that makes the use of a particular medication unsafe or inadvisable.

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Cross Sensitivity

A condition in which a patient allergic to one drug experiences an allergic reaction when exposed to a structurally related medication.

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Cytochrome P450 (CYP 450) Enzymes

A family of specialized hepatic enzymes (such as CYP 3A4 and CYP 2C9) responsible for metabolizing medications and frequently involved in drug interactions.