Generic names, brand names, and classifications of medications
Therapeutic equivalence
Common and life-threatening drug interactions and contradictions (e.g., drug-disease, drug-drug, drug-dietary supplement, drug-laboratory, drug-nutrient)
Strengths/dose, dosage forms, routes of administration, special handling and administration instructions, and duration of drug therapy
Common and severe medication side effects, adverse effects, and allergies
Indications of medications and dietary supplements
Drug stability (e.g., oral suspensions, insulin, reconstitutables, injectables, vaccinations)
Narrow therapeutic index (NTI) medications
Physical and chemical incompatibilities related to non-sterile compounding and reconstitution
Proper storage of medications (e.g., temperature ranges, light sensitivity, restricted access)
Federal Requirements
Federal requirements for handling and disposal of non-hazardous, hazardous, and pharmaceutical substances and waste
Federal requirements for controlled substance prescriptions (i.e., new, refill, transfer) and DEA controlled substance schedules
Federal requirements (e.g., DEA, FDA) for controlled substances (i.e., receiving, storing, ordering, labeling, dispensing, reverse distribution, take-back programs, or loss or theft of)
Federal requirements for restricted drug programs and related medication processing (e.g., pseudoephedrine, Risk Evaluation and Mitigation Strategies [REMS])
FDA recall requirements (e.g., medications, devices, supplies, supplements, classifications)
Patient Safety and Quality Assurance
High-alert/risk medications and look-alike/sound-alike [LASA] medications
Error prevention strategies (e.g., prescription or medication order to correct patient, Tall Mann lettering, separating inventory, leading and trailing zeros, bar code usage, limit use of error-prone abbreviations)
Issues that require pharmacist intervention (e.g., drug utilization review [DUR], adverse drug event [ADE], OTC recommendation, therapeutic substitution, misuse, adherence, post-immunization follow-up, allergies, drug interactions)
Event reporting procedures (e.g., medication errors, adverse effects, and products integrity, MedWatch, near miss, root-cause analysis [RCA])
Types of prescription errors (e.g., abnormal doses, early refill, incorrect quantity, incorrect patient, incorrect drug)
Hygiene and cleaning standards (e.g., handwashing, personal protective equipment [PPE], cleaning counting trays, countertop, and equipment)
Formulas, calculations, ratios, proportions, allegations, conversions, Sig codes (e.g., b.i.d., t.i.d., Roman numerals), abbreviations, medical terminology, and symbols for days supply, quantity, dose, concentration, dilutions
Equipment/supplies required for drug administration (e.g., package size, unit dose, diabetic supplies, spacers, oral and injectable syringes)
Lot numbers, expiration dates, and National Drug Code (NDC) numbers
Procedures for identifying and returning dispensable, non-dispensable, and expired medications and supplies (e.g., credit return, return to stock, reverse distribution)
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