Medications (35%)
- Brand/generic names and classes; therapeutic duplications
- Drug interactions and contraindications (drug-drug, -nutrient, -disease)
- Doses, dosage forms, routes; stability and beyond-use dating
- Side effects, indications, and proper storage (temperature, light)
Federal Requirements (18.75%)
- DEA schedules; refill rules (C-II none; C-III/IV up to 5 in 6 months)
- DEA forms: 222 ordering C-II, 106 theft/loss, 41 destruction
- Restricted programs: pseudoephedrine limits, REMS
- FDA recalls (Class I–III) and DSCSA tracking and tracing
Patient Safety and Quality Assurance (23.75%)
- High-alert and look-alike/sound-alike drugs; Tall Man lettering
- Error prevention: leading zero yes, trailing zero no; avoid "U"
- When to refer to the pharmacist (DUR, OTC advice, interactions)
- Reporting: MedWatch (drugs/devices), VAERS (vaccines); infection control
Order Entry and Processing (22.5%)
- Sig codes and abbreviations (bid, tid, gtt, OU/OD/OS, AU)
- Days' supply, quantity, weight-based dose, concentration math
- NDC segments: labeler, product, package; lot numbers and expiration
- Returns: return to stock, credit returns, reverse distribution
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