Glossary
The terms, abbreviations, and forms you have to know — in plain English. Filter by domain or search.
367 terms
- -azoleMedications
- Antifungals that block ergosterol synthesis in the fungal cell membrane; e.g., fluconazole, ketoconazole.
- -caineMedications
- Local anesthetics that numb tissue by blocking nerve signals; e.g., lidocaine, benzocaine.
- -cillinMedications
- Penicillin-class antibiotics that kill bacteria by disrupting cell-wall synthesis; e.g., amoxicillin.
- -cyclineMedications
- Tetracycline-class antibiotics; broad-spectrum, avoid with dairy/antacids; e.g., doxycycline.
- -dipineMedications
- Suffix for calcium channel blockers (e.g., amlodipine)
- -floxacinMedications
- Suffix for fluoroquinolone antibiotics (e.g., ciprofloxacin)
- -gliptinMedications
- DPP-4 inhibitors that lower blood sugar; e.g., sitagliptin.
- -glitazoneMedications
- Diabetes drugs improving insulin sensitivity; e.g., pioglitazone.
- -mabMedications
- Monoclonal antibody biologics targeting specific proteins; e.g., adalimumab.
- -mycin / -micinMedications
- Antibiotic suffix seen in aminoglycosides and macrolides; e.g., azithromycin, gentamicin.
- -nibMedications
- Kinase-inhibitor cancer drugs that block tumor-growth signals; e.g., imatinib.
- -ololMedications
- Suffix for beta blockers (e.g., metoprolol)
- -pam / -lamMedications
- Benzodiazepines for anxiety/seizures; enhance GABA; e.g., diazepam, lorazepam, alprazolam.
- -parinMedications
- Anticoagulant heparins that prevent clots; e.g., enoxaparin, dalteparin.
- -prazoleMedications
- Suffix for proton pump inhibitors (PPIs)
- -prilMedications
- Suffix for ACE inhibitors (e.g., lisinopril)
- -sartanMedications
- Suffix for ARBs (e.g., losartan)
- -statinMedications
- Suffix for cholesterol-lowering statins
- -terolMedications
- Beta-2 agonist bronchodilators that open airways; e.g., albuterol, salmeterol.
- -tidineMedications
- H2 blockers that reduce stomach acid; e.g., famotidine, cimetidine (ranitidine was withdrawn in 2020).
- -triptanMedications
- Migraine drugs that constrict cranial blood vessels; e.g., sumatriptan.
- -virMedications
- Antiviral drugs that inhibit viral replication; e.g., acyclovir, oseltamivir.
- -zosinMedications
- Alpha-1 blockers that relax blood vessels and the prostate; e.g., prazosin, doxazosin, terazosin.
- 1 gr = 65 mgOrder Entry & Processing
- Apothecary grain to milligram conversion.
- 1 kg = 2.2 lbOrder Entry & Processing
- Kilogram to pound conversion for weight-based dosing.
- 1 lb = 454 gOrder Entry & Processing
- Pound to gram conversion for weight.
- 1 oz = 30 mLOrder Entry & Processing
- Approximate fluid ounce to milliliter conversion.
- 1 tbsp = 15 mLOrder Entry & Processing
- Standard household-to-metric conversion for a tablespoon.
- 1 tsp = 5 mLOrder Entry & Processing
- Standard household-to-metric conversion for a teaspoon.
- 340BOrder Entry & Processing
- A federal program letting qualifying safety-net facilities buy outpatient drugs at deeply discounted prices.
- 5% w/vOrder Entry & Processing
- 5 grams per 100 mL
- 72-hour emergency supplyFederal Requirements
- State-law allowance (length varies by state) letting a pharmacist dispense a short emergency supply when the prescriber cannot be reached.
- A1cMedications
- Hemoglobin A1c — a blood test reflecting average glucose over roughly the past three months, so it shows long-term diabetes control rather than a single moment.
- aaOrder Entry & Processing
- Of each; equal amounts of listed ingredients.
- ACOrder Entry & Processing
- Before meals
- ac & hsOrder Entry & Processing
- Before meals and at bedtime (four times daily).
- ADOrder Entry & Processing
- Right ear (auris dextra).
- Additive effectMedications
- When two drugs with the same effect stack, so the risk adds up even though neither dose is wrong on its own. It is why a duplication matters.
- AdjudicationOrder Entry & Processing
- Real-time claim submission to insurer determining coverage and copay.
- AdjuvantMedications
- An ingredient added to a vaccine to strengthen the immune response. Two-component vaccines mix the antigen with its adjuvant at reconstitution and must then be used within a set time.
- Administration errorPatient Safety & Quality Assurance
- A mistake made when the drug is actually given to the patient.
- Adverse drug eventPatient Safety & Quality Assurance
- Any injury resulting from the use of a medication, whether preventable or not.
- Adverse drug reactionPatient Safety & Quality Assurance
- An unintended, harmful response to a drug given at normal doses.
- Alert fatiguePatient Safety & Quality Assurance
- What happens when a system fires so many warnings that people stop reading them. The fix is fewer, better alerts — not telling staff to try harder.
- AlligationOrder Entry & Processing
- Mixing two strengths to reach a target strength
- AmbienMedications
- Brand name for zolpidem, a sedative-hypnotic for sleep
- AmoxilMedications
- Brand name for amoxicillin, a penicillin antibiotic
- Anabolic Steroid Control ActFederal Requirements
- Placed anabolic steroids into Schedule III of the CSA.
- ANCMedications
- Absolute neutrophil count — the number of a specific infection-fighting white cell. Clozapine requires ANC monitoring because it can cause severe neutropenia.
- AnteroomPatient Safety & Quality Assurance
- Transition area for hand hygiene and garbing before the buffer area.
- AnticholinergicMedications
- Blocks acetylcholine. The predictable set follows: dry mouth, blurred vision, constipation, urinary retention and confusion — which is why these drugs are risky in older adults and in men with an enlarged prostate.
- AntihistamineMedications
- Blocks histamine to treat allergy symptoms. First-generation agents like diphenhydramine cross into the brain and sedate; second-generation agents like loratadine largely do not.
- ARBMedications
- Angiotensin receptor blocker; lowers blood pressure; generics end in -sartan.
- ARCOSFederal Requirements
- The DEA system that tracks controlled substances moving between manufacturers and distributors. It is a supply-chain tool, not a patient-level database like a PDMP.
- ASOrder Entry & Processing
- Left ear (auris sinistra).
- AUOrder Entry & Processing
- Both ears (auris utraque).
- Authorized collectorFederal Requirements
- A pharmacy or other registrant that has modified its DEA registration so it may accept unused controlled substances back from patients. It is an opt-in status, not automatic.
- Auxiliary labelOrder Entry & Processing
- Supplemental warning sticker (e.g., "Take with food") added to a prescription.
- AWPOrder Entry & Processing
- Average Wholesale Price, a drug pricing benchmark
- Barcode medication administrationPatient Safety & Quality Assurance
- Scanning drug and patient barcodes to verify the right dose at bedside.
- Basal insulinMedications
- A long-acting insulin such as glargine that gives steady background coverage through the day, as opposed to a mealtime insulin taken with food.
- Benzalkonium chlorideMedications
- A preservative in many eye drops. It absorbs into contact lenses, so lenses come out before the drop and go back in about 15 minutes later.
- Beta blockerMedications
- Slows heart rate and lowers blood pressure by blocking adrenaline; ends in -olol.
- Beyond-use datePatient Safety & Quality Assurance
- The date after which a product should no longer be used. For a DISPENSED container it can be no later than the manufacturer expiration, and no more than one year from dispensing. Repackaged unit-dose follows a stricter rule: the earliest of six months, 25% of the time remaining, or the manufacturer expiration.
- BIDOrder Entry & Processing
- Twice daily
- Biennial inventoryFederal Requirements
- A controlled-substance count taken every 2 years
- BINOrder Entry & Processing
- Bank Identification Number routing the insurance claim.
- BioavailabilityMedications
- The share of a dose that actually reaches the bloodstream in active form. Swallowing a sublingual product wastes most of it — partly poor absorption, partly first-pass metabolism.
- Biological safety cabinetPatient Safety & Quality Assurance
- Vertical-airflow hood protecting worker and product when compounding hazardous drugs.
- Black box warningPatient Safety & Quality Assurance
- FDA's strongest label warning, officially called a boxed warning, about serious or life-threatening drug risks.
- Boxed warningMedications
- The most serious warning the FDA can require on a drug label, printed inside a black border. It flags a risk that can be fatal or permanently disabling.
- BradykininMedications
- A substance ACE normally breaks down. ACE inhibitors let it build up, which causes the dry cough. ARBs do not block that enzyme, so switching to one usually clears the cough.
- BuccalMedications
- Medication placed between cheek and gum to dissolve.
- Buffer areaPatient Safety & Quality Assurance
- Cleanroom zone housing the hood where sterile compounding takes place.
- C1V1 = C2V2Order Entry & Processing
- The dilution equation: concentration times volume before equals concentration times volume after. Because the amount of active drug does not change when you add diluent, a stronger, smaller volume becomes a weaker, larger one — solve for whichever of the four values is missing. Example: to make 100 mL of 5% from a 25% stock, V1 = (5 x 100) / 25 = 20 mL of stock, then add diluent to 100 mL.
- Calcium channel blockerMedications
- Relaxes blood vessels and slows heart; many end in -dipine.
- capOrder Entry & Processing
- Capsule dosage form.
- CapitationOrder Entry & Processing
- A payment model where the plan pays a fixed amount per patient per period, regardless of how much that patient uses.
- CardioselectiveMedications
- A beta blocker that acts mainly on beta-1 receptors in the heart, such as metoprolol or atenolol. Selectivity is RELATIVE, not absolute — it fades at higher doses, so caution in asthma still applies.
- CardizemMedications
- Brand name for diltiazem, a calcium channel blocker
- Chemo gownPatient Safety & Quality Assurance
- Disposable, closed-front gown of tested low-permeability material worn when handling hazardous drugs.
- Chemotherapy glovesPatient Safety & Quality Assurance
- Thicker, tested gloves worn, often double, when handling hazardous drugs.
- Chemotherapy spill kitPatient Safety & Quality Assurance
- Supplies used to safely contain and clean up a hazardous drug spill.
- Child-resistantPatient Safety & Quality Assurance
- Packaging designed so most young children cannot open it quickly. It is child-RESISTANT, not childproof, and it is a different thing from tamper-evident.
- Class I recallFederal Requirements
- Reasonable probability of serious harm or death
- Class III recallFederal Requirements
- Not likely to cause adverse health effects
- Closed system transfer devicePatient Safety & Quality Assurance
- Device preventing hazardous drug vapor or liquid from escaping during transfer.
- CoinsuranceOrder Entry & Processing
- Percentage of drug cost the patient pays.
- Collection receptacleFederal Requirements
- The locked container an authorized collector uses to take back unused medicines. Contents may never be counted, sorted, inventoried, or individually handled.
- Combat Methamphetamine Epidemic Act (CMEA)Federal Requirements
- 2005 law restricting sale of pseudoephedrine and other meth precursors.
- Compounding aseptic isolatorPatient Safety & Quality Assurance
- Enclosed glovebox providing a sterile environment for compounding sterile preparations.
- ConsigneePatient Safety & Quality Assurance
- Anyone who received a recalled product from the firm — including your pharmacy. Firms must account for every consignee, which is why you answer a recall notice even holding none of the lot.
- Contact timePatient Safety & Quality Assurance
- How long a disinfectant must stay visibly wet on a surface to work. Wiping it dry early means the surface was not disinfected.
- ContraindicationMedications
- A condition making a drug unsafe to use for a patient.
- Control solutionOrder Entry & Processing
- A liquid of known glucose value used to check that a meter and its strips are reading correctly. Not a cleaner and not a treatment.
- Controlled Rx transferFederal Requirements
- CIII-CV prescriptions transfer one time only (or shared refills on same real-time database).
- Controlled Substances Act (CSA)Federal Requirements
- 1970 law creating the drug schedules and regulating controlled-substance manufacture and distribution.
- CopayOrder Entry & Processing
- Fixed amount the patient pays per prescription.
- Corresponding responsibilityFederal Requirements
- Pharmacist shares legal duty to ensure a controlled Rx is legitimate.
- CoumadinMedications
- Brand name for warfarin, an anticoagulant
- CozaarMedications
- Brand name for losartan, an ARB
- Credit returnOrder Entry & Processing
- Sending damaged, incorrect, or short-dated stock back to the supplier or wholesaler for account credit.
- CSOSFederal Requirements
- Controlled Substance Ordering System: DEA-approved electronic ordering of any schedule, with no paper Form 222
- CSOS digital certificateFederal Requirements
- The credential for ordering controlled substances electronically. It is issued to ONE named person, cannot be shared or backed up, and a power of attorney does not let you use someone else's.
- CYP2D6Medications
- A liver enzyme that varies between people. Ultra-rapid metabolizers convert codeine to morphine unusually fast, which is why codeine is contraindicated in children after tonsillectomy.
- Data entryOrder Entry & Processing
- Workflow step entering prescription details into the pharmacy system.
- DAWOrder Entry & Processing
- Dispense As Written: a substitution code
- DAW 0Order Entry & Processing
- No product selection indicated; generic substitution allowed.
- DAW 1Order Entry & Processing
- Prescriber requires brand; substitution not allowed.
- DAW 2Order Entry & Processing
- Patient requested brand-name product.
- Days supplyOrder Entry & Processing
- Total quantity divided by amount used per day
- DEAFederal Requirements
- Enforces the Controlled Substances Act and registers handlers of controlled drugs.
- DEA Form 106Federal Requirements
- Reports theft or significant loss of controlled substances
- DEA Form 222Federal Requirements
- Orders Schedule I and II controlled substances
- DEA Form 223Federal Requirements
- The certificate of registration DEA issues, including after a modification such as a name or address change.
- DEA Form 224Federal Requirements
- Application to register a pharmacy with the DEA
- DEA Form 225Federal Requirements
- Registration application for manufacturers, distributors, importers, and exporters of controlled substances.
- DEA Form 41Federal Requirements
- Records the destruction of controlled substances
- DEA numberFederal Requirements
- Registrant identifier verified by a checksum of its digits; format is two letters plus seven digits.
- DeductibleOrder Entry & Processing
- Amount patient pays before insurance begins covering costs.
- DeltasoneMedications
- Brand name for prednisone, a corticosteroid
- Deteriorated drug errorPatient Safety & Quality Assurance
- NCC MERP type 70.13 — dispensing a product that has expired or degraded. Distinct from an omission, a monitoring error, or a wrong dose.
- Digital data loggerPatient Safety & Quality Assurance
- The thermometer used to monitor vaccine storage. Its probe sits in a buffered solution such as glycol so it reflects the temperature of the vaccine, not the air, which swings every time the door opens.
- Dimensional analysisOrder Entry & Processing
- Calculation using unit conversion factors to cancel units.
- dispOrder Entry & Processing
- Dispense; the quantity to be given.
- DispenserFederal Requirements
- DSCSA term for the pharmacy — the trading partner that gets the drug to the patient.
- Dispensing errorPatient Safety & Quality Assurance
- A mistake made in the pharmacy while filling or labeling a prescription.
- Do Not Use listPatient Safety & Quality Assurance
- Joint Commission list of abbreviations banned to prevent misreading.
- Dose counterOrder Entry & Processing
- The counter on a metered-dose inhaler. It is the only reliable end-point: the canister keeps spraying past 000 even though the dose is no longer assured, so floating or shaking it proves nothing.
- Drug Facts labelMedications
- The standardized OTC label panel: Active ingredients, Purpose, Uses, Warnings, Directions. Reading it is how you spot a duplicate active ingredient across two products.
- Drug library (DERS)Patient Safety & Quality Assurance
- The dose limits programmed into a smart infusion pump. Running the pump in basic mode bypasses them, which is why library bypass is tracked as a safety event.
- Drug-disease contraindicationPatient Safety & Quality Assurance
- A DUR category: the drug is unsafe given a condition the patient already has, such as a non-selective beta blocker in asthma.
- Dry powder inhaler (DPI)Medications
- An inhaler with no propellant — your own fast, deep breath lifts the powder. It never takes a spacer, and you must never breathe out into it, because moisture clumps the powder.
- DSCSAFederal Requirements
- Drug Supply Chain Security Act; builds electronic track-and-trace across the drug supply chain.
- Ductus arteriosusMedications
- A fetal blood vessel that must stay open until birth. NSAIDs can close it early, which is why they are avoided from about 30 weeks.
- DUROrder Entry & Processing
- Drug utilization review; automated safety check during adjudication.
- DUR alertOrder Entry & Processing
- System warning of interactions, duplications, or dosing concerns.
- Durham-Humphrey AmendmentFederal Requirements
- 1951 law distinguishing prescription (legend) drugs from OTC drugs.
- eGFRMedications
- Estimated glomerular filtration rate — a calculated measure of how well the kidneys filter. Drug labels use it to set dose limits; metformin is contraindicated below 30.
- ElixirMedications
- Clear, sweetened, alcohol-containing oral liquid dosage form.
- Emergency Schedule IIFederal Requirements
- Oral order allowed; written Rx must follow within 7 days
- Enteric-coatedMedications
- Coating that delays release until the intestine; do not crush.
- Error-prone abbreviationsPatient Safety & Quality Assurance
- Shorthand like U, QD, or MSO4 that ISMP says to spell out.
- ETASUFederal Requirements
- Elements To Assure Safe Use — the strictest REMS requirements, the ones that actually gate dispensing: certified prescribers, certified pharmacies, enrolled patients, or restricted settings. A Medication Guide is NOT an ETASU.
- Expiration dateOrder Entry & Processing
- Manufacturer's date guaranteeing potency of the original product.
- Exposure incidentPatient Safety & Quality Assurance
- A needlestick, cut or splash involving potentially infectious material. OSHA requires the employer to provide confidential medical evaluation and follow-up at no cost to the employee.
- Failure mode and effects analysisPatient Safety & Quality Assurance
- Proactive review predicting how a process could fail before errors happen.
- FDAFederal Requirements
- Regulates drug approval, safety, labeling, and manufacturing quality.
- FDA Adverse Event Reporting SystemPatient Safety & Quality Assurance
- FDA database (FAERS) collecting adverse event and medication error reports.
- FDCA (1938)Federal Requirements
- Food, Drug, and Cosmetic Act requiring premarket safety proof after sulfanilamide deaths.
- Federal transfer warningFederal Requirements
- Label statement: transfer of this drug to anyone other than the patient is illegal.
- Filter needleOrder Entry & Processing
- A needle with a built-in filter, used to draw medication out of a glass ampule so glass fragments stay behind. Swap it for a regular needle before injecting.
- First airPatient Safety & Quality Assurance
- Clean air flowing directly from a HEPA filter to a critical site.
- First-pass metabolismMedications
- The liver breaking a drug down after oral absorption, before it reaches the bloodstream. Sublingual, buccal, rectal and injected routes bypass it, which is why the same drug can need a very different dose by mouth.
- Five rightsPatient Safety & Quality Assurance
- Right patient, drug, dose, route, and time
- FormularyOrder Entry & Processing
- Insurer's list of covered/preferred medications.
- GarbingPatient Safety & Quality Assurance
- Putting on protective attire in order before entering a compounding cleanroom.
- Geometric dilutionOrder Entry & Processing
- Mixing potent drug with base in gradually increasing amounts.
- GlucophageMedications
- Brand name for metformin (type 2 diabetes)
- gttOrder Entry & Processing
- Drop(s)
- Half-lifeMedications
- Time for blood drug concentration to drop by half; guides dosing frequency.
- HemolysisPatient Safety & Quality Assurance
- Red blood cells rupturing. It is what happens when a hypotonic fluid such as plain sterile water is infused.
- HEPA filterPatient Safety & Quality Assurance
- Removes at least 99.97% of 0.3-micron particles
- Hepatitis B vaccination (OSHA)Patient Safety & Quality Assurance
- The employer must OFFER hepatitis B vaccination at no cost within 10 working days of assignment to at-risk duties. An employee who declines signs a declination and may still request it later, free.
- High-alert medicationPatient Safety & Quality Assurance
- Can cause severe harm if given in error (e.g., insulin)
- HIPAAFederal Requirements
- Protects patient health information (PHI)
- Hospital internal codeFederal Requirements
- A suffix the hospital appends to its own DEA number for a resident or staff prescriber who has no personal registration, written after a hyphen. The hospital keeps a list you can verify against.
- HPA axis suppressionMedications
- The body slowing its own steroid production because a potent steroid is being absorbed. It is why high-potency topical steroids carry limits on amount, duration, and covering the area.
- HSOrder Entry & Processing
- At bedtime
- HyperkalemiaMedications
- High blood potassium. ACE inhibitors, ARBs and potassium-sparing diuretics like spironolactone all push it up, which is why potassium is watched when they are combined.
- HypokalemiaMedications
- Low blood potassium. It sensitizes the heart to digoxin, so toxicity can occur even when the digoxin level looks acceptable.
- HypotonicPatient Safety & Quality Assurance
- Thinner than blood. Sterile Water for Injection is hypotonic, so infusing it without a solute pulls water into red cells until they burst — which is why it is a diluent, never an infusion.
- IDOrder Entry & Processing
- Intradermal; into the skin.
- IMOrder Entry & Processing
- Intramuscular (into the muscle)
- Incident reportPatient Safety & Quality Assurance
- An internal record of a safety event, written in objective factual terms without blame. It goes to the pharmacy quality process, not into the patient chart.
- Incidental disclosureFederal Requirements
- Protected health information overheard as a by-product of a permitted conversation. It is not a HIPAA breach as long as reasonable safeguards were in place.
- Independent double checkPatient Safety & Quality Assurance
- A second person verifies a high-alert dose
- Initial inventoryFederal Requirements
- Complete controlled-substance count taken when a pharmacy first begins dispensing.
- INRMedications
- International Normalized Ratio — a standardized measure of how long blood takes to clot. It is how warfarin therapy is monitored; a typical atrial-fibrillation target is 2 to 3.
- InscriptionOrder Entry & Processing
- Part of the Rx naming the drug, strength, and quantity.
- IntolerancePatient Safety & Quality Assurance
- An unpleasant but non-immune reaction, such as nausea. Recording it as an allergy can wrongly block a whole drug class the patient could safely take.
- Intradermal (ID)Order Entry & Processing
- Into the skin itself, almost flat to the surface, raising a small wheal. It is the tuberculin skin-test route — shallower than subcutaneous.
- Inventory turnoverOrder Entry & Processing
- How many times a year a pharmacy sells through its stock: annual cost of goods sold divided by average inventory value. Higher means less cash sitting on the shelf.
- ISMPPatient Safety & Quality Assurance
- Institute for Safe Medication Practices
- ISO Class 5Patient Safety & Quality Assurance
- Cleanliness standard for the critical area where sterile compounding occurs.
- IVMedications
- Intravenous; medication given directly into a vein.
- Kefauver-Harris AmendmentFederal Requirements
- 1962 law that ADDED proof of effectiveness to the existing safety requirement, after the thalidomide tragedy. Safety alone was already required by the 1938 FDCA — effectiveness is what this amendment introduced.
- Labeler codeOrder Entry & Processing
- The first NDC segment, assigned by the FDA to the manufacturer, REPACKAGER or relabeler. A repackager holds its own code, so a repackaged bottle carries its NDC rather than the original manufacturer's.
- Laminar airflow hoodPatient Safety & Quality Assurance
- Provides ISO Class 5 air for sterile compounding
- LancetOrder Entry & Processing
- A small blade or point used to prick the skin for a blood glucose sample. It is held by a lancing device that sets the depth.
- LASAPatient Safety & Quality Assurance
- Look-alike/sound-alike drug names
- LasixMedications
- Brand name for furosemide, a loop diuretic
- Leading zeroPatient Safety & Quality Assurance
- Write 0.5 mg, never .5 mg, to prevent 10-fold errors
- Legend drugFederal Requirements
- Prescription-only drug bearing "Rx only" on its label.
- LevigationOrder Entry & Processing
- Grinding a powder with a small amount of liquid to reduce particle size before mixing.
- Light-resistant containerPatient Safety & Quality Assurance
- A container that blocks enough light to protect a photosensitive drug. Repackaging into a clear vial destroys that protection — though an opaque outer covering or secondary packaging can restore it.
- LipitorMedications
- Brand name for atorvastatin, a statin
- LipodystrophyMedications
- Lumpy or pitted changes in fat under the skin from injecting the same spot repeatedly. Rotating injection sites prevents it, and it also makes absorption unpredictable.
- Loop diureticMedications
- A strong diuretic such as furosemide that acts on the loop of Henle. It dumps potassium, which is why potassium is monitored and why it is sometimes paired with a potassium-sparing agent.
- Market withdrawalFederal Requirements
- A firm removing a product for a minor issue that would not trigger legal action by the FDA. It is not a recall.
- MedGuidePatient Safety & Quality Assurance
- FDA-required patient handout warning of serious risks for certain drugs.
- Medication errorPatient Safety & Quality Assurance
- Any preventable event that may cause inappropriate medication use or patient harm.
- Medication reconciliationPatient Safety & Quality Assurance
- Comparing a patient's medication list across care transitions to prevent errors.
- MedWatchPatient Safety & Quality Assurance
- FDA program for reporting adverse drug events
- mEqMedications
- Milliequivalent — a measure of the amount of an electrolyte, used for potassium, sodium and calcium salts. Potassium chloride 750 mg equals 10 mEq.
- MERPPatient Safety & Quality Assurance
- ISMP's Medication Errors Reporting Program collecting reports to prevent future errors.
- Minimum necessaryFederal Requirements
- Use or share only the PHI a task requires
- Monitoring errorPatient Safety & Quality Assurance
- An NCC MERP error type: the patient was not watched the way the drug requires, such as a level or lab that should have been drawn and was not.
- Multi-dose vialPatient Safety & Quality Assurance
- A vial meant for more than one withdrawal. Use a NEW needle and a NEW syringe for every entry, and disinfect the septum first — a used syringe contaminates the vial for everyone after.
- Narrow therapeutic indexMedications
- A drug where the effective dose and the toxic dose sit close together, so small changes in blood level matter. Warfarin, lithium, digoxin and phenytoin are the classic examples.
- NDCOrder Entry & Processing
- 10-digit code on the label (padded to 11 digits for billing): labeler, product, package
- NDC barcode scanPatient Safety & Quality Assurance
- Scanning the stock bottle during fill to confirm the correct product.
- NDC numberFederal Requirements
- 10- or 11-digit code identifying labeler, product, and package size.
- Near missPatient Safety & Quality Assurance
- An error that is caught before it reaches the patient. If it reached the patient but caused no harm, that is a no-harm error (NCC MERP Category C), not a near miss.
- NebulizerOrder Entry & Processing
- A device that turns liquid medication into a mist breathed in over several minutes. Needs no coordination, so it suits small children and patients in distress.
- Needle gaugeOrder Entry & Processing
- How thick a needle is — and it runs backwards: the HIGHER the gauge number, the thinner the needle. A 30 G needle is finer than an 18 G.
- Negative pressure roomPatient Safety & Quality Assurance
- Room where air flows inward to contain hazardous drug contamination.
- NeurontinMedications
- Brand name for gabapentin (nerve pain and seizures)
- NeutropeniaMedications
- An abnormally low neutrophil count, leaving the patient vulnerable to infection. Severe neutropenia is the reason clozapine requires ongoing ANC monitoring.
- NexiumMedications
- Brand name for esomeprazole, a proton pump inhibitor
- NIOSH hazardous drug listPatient Safety & Quality Assurance
- List published by NIOSH, a CDC agency, naming drugs that need special handling; USP <800> is the standard that requires following it.
- Non-retrievableFederal Requirements
- The DEA destruction standard: the controlled substance must be permanently altered so it can never be used by anyone again. It does not require a DEA agent to witness the destruction.
- NorvascMedications
- Brand name for amlodipine, a calcium channel blocker
- NSAIDMedications
- Non-steroidal anti-inflammatory drug for pain/inflammation; e.g., ibuprofen, naproxen.
- OBRA '90Federal Requirements
- Requires pharmacists to offer counseling and perform drug utilization review for Medicaid patients.
- Occlusive dressingMedications
- Covering a topical medicine with a bandage or wrap. It drives far more drug into the skin, which is why potent steroids say not to do it unless a prescriber directs it.
- ODOrder Entry & Processing
- Right eye (oculus dexter).
- OligohydramniosMedications
- Too little amniotic fluid around the fetus. NSAIDs can cause it from about 20 weeks of pregnancy, which is why use is limited from then on.
- Omission errorPatient Safety & Quality Assurance
- Failure to give a scheduled or ordered dose of medication.
- One-time CII transferFederal Requirements
- An electronic CII prescription may be transferred once between pharmacies for initial dispensing.
- Ophthalmic vs oticMedications
- Ophthalmic means for the eye and must be sterile; otic means for the ear. An ophthalmic product may be used in the ear when directed, but an ear drop must NEVER go in the eye.
- Oral syringeOrder Entry & Processing
- A syringe for liquid doses taken by mouth. It will not accept a needle, which is exactly what makes it safe — an oral dose can never be injected by mistake.
- Orally disintegrating tablet (ODT)Medications
- A tablet that dissolves on the tongue without water. Handle it with dry hands and peel the foil back rather than pushing the tablet through it.
- OSOrder Entry & Processing
- Left eye (oculus sinister).
- OTC monographFederal Requirements
- An FDA rulebook setting the ingredients, doses and labeling an over-the-counter category may use. A product that conforms needs no new drug application.
- OUOrder Entry & Processing
- Both eyes (oculus uterque).
- P-listFederal Requirements
- The EPA’s list of acutely hazardous wastes under RCRA. Warfarin above 0.3% is P001 — the same drug is a clinical medicine on the shelf and a listed hazardous waste once discarded.
- P075Federal Requirements
- The EPA hazardous-waste code for nicotine and its salts. The listing excludes FDA-approved OTC patches, gums and lozenges; prescription nicotine products remain listed.
- Package codeOrder Entry & Processing
- Last NDC segment identifying the package size and type.
- Partial fill (CII)Federal Requirements
- If the pharmacy cannot supply the full amount, the rest must be filled within 72 hours; a partial fill requested by patient or prescriber may be completed within 30 days.
- PCOrder Entry & Processing
- After meals
- PCAPatient Safety & Quality Assurance
- Patient-controlled analgesia: an infusion pump the patient triggers for pain relief. The safeguard is that only the patient presses the button; someone else pressing it (PCA by proxy) defeats it.
- PCNOrder Entry & Processing
- Processor Control Number directing claim to correct plan.
- PDMPFederal Requirements
- Prescription Drug Monitoring Program — a STATE-run database of dispensed controlled substances. There is no national DEA PDMP.
- Peak and troughMedications
- Two timed blood levels: the peak is drawn after a dose has distributed, the trough immediately BEFORE the next dose. Used for aminoglycosides and vancomycin.
- Peak flow meterOrder Entry & Processing
- A handheld device that measures how fast a patient can blow air out. It monitors asthma control; it does not deliver any medication.
- Pen needleOrder Entry & Processing
- The disposable needle screwed onto an insulin pen for each injection. Pens are dispensed without needles, so these are supplied alongside.
- Perpetual inventoryFederal Requirements
- Running count of Schedule II stock updated with each receipt and dispense.
- Personal protective equipmentPatient Safety & Quality Assurance
- Gowns, gloves, and masks worn to protect against exposure and contamination.
- Piggyback (secondary set)Order Entry & Processing
- A small-volume IV bag hung above the primary bag so it infuses first, commonly used for intermittent antibiotic doses.
- PlavixMedications
- Brand name for clopidogrel, an antiplatelet
- POOrder Entry & Processing
- By mouth
- Post-exposure prophylaxis (PEP)Patient Safety & Quality Assurance
- Treatment started after a needlestick or splash to prevent infection. OSHA requires the employer to provide evaluation, source testing, PEP when medically indicated, and counseling at no cost.
- Potassium-containing salt substituteMedications
- A table-salt replacement made from potassium chloride. Harmless for most people, but a real hazard with ACE inhibitors, ARBs or spironolactone, which already raise potassium.
- Potassium-sparing diureticMedications
- A diuretic such as spironolactone that removes fluid without dumping potassium — it blocks aldosterone. Paired with a loop diuretic it offsets potassium loss; combined with an ACE inhibitor it can push potassium too high.
- Power of Attorney (DEA 222)Federal Requirements
- Written authorization letting an agent sign DEA Form 222 orders for the registrant.
- PPIMedications
- Proton pump inhibitor that strongly reduces stomach acid; ends in -prazole.
- PPPAFederal Requirements
- Poison Prevention Packaging Act: child-resistant containers
- PRMedications
- Per rectum; rectal route of administration.
- PR (per rectum)Order Entry & Processing
- By rectum. Chosen when a patient cannot keep anything down, and it partly bypasses first-pass metabolism.
- Prescribing errorPatient Safety & Quality Assurance
- A mistake in drug selection, dose, route, or directions made at ordering.
- PrilosecMedications
- Brand name for omeprazole, a proton pump inhibitor
- Prior authorizationOrder Entry & Processing
- Insurer approval required before a drug is covered.
- PRNOrder Entry & Processing
- As needed
- ProAirMedications
- Brand name for albuterol, a rescue bronchodilator
- Product codeOrder Entry & Processing
- Middle NDC segment identifying drug, strength, and form.
- ProphylaxisMedications
- Using a medication to prevent disease rather than treat it.
- PSE logbookFederal Requirements
- Record of PSE sales kept two years with buyer name, address, and ID.
- Pseudoephedrine 30-day limitFederal Requirements
- 9 grams per customer per 30 days (7.5 g if mail-order).
- Pseudoephedrine daily limitFederal Requirements
- 3.6 grams per customer per day of PSE base may be sold.
- Pure Food and Drug ActFederal Requirements
- 1906 law prohibiting misbranded and adulterated drugs; first major federal drug law.
- PVOrder Entry & Processing
- Per vagina; vaginal route of administration.
- q4hOrder Entry & Processing
- Every 4 hours around the clock.
- q6hOrder Entry & Processing
- Every 6 hours
- q8hOrder Entry & Processing
- Every 8 hours around the clock.
- qAMOrder Entry & Processing
- Every morning.
- QDOrder Entry & Processing
- Once daily (every day); on ISMP error-prone list, spell out "daily".
- qHSOrder Entry & Processing
- Every night at bedtime.
- QIDOrder Entry & Processing
- Four times daily
- QODOrder Entry & Processing
- Every other day; error-prone abbreviation, spell out "every other day".
- qPMOrder Entry & Processing
- Every evening.
- qsOrder Entry & Processing
- Quantity sufficient; add enough to reach a total.
- Quality assurancePatient Safety & Quality Assurance
- Ongoing system of checks confirming pharmacy processes meet safety standards.
- QuarantinePatient Safety & Quality Assurance
- Physically separating suspect or recalled stock and marking it clearly so it cannot be selected. Not the same as discarding it — the notice decides its fate.
- Ratio-proportionOrder Entry & Processing
- Calculation method solving one unknown from equal ratios.
- RCRAFederal Requirements
- The Resource Conservation and Recovery Act — the federal law, administered by the EPA, that governs hazardous waste including discarded pharmaceuticals.
- Read-backPatient Safety & Quality Assurance
- Repeating a verbal order back to the prescriber, spelling look-alike drug names and confirming the dose, before it is accepted.
- Readily retrievableFederal Requirements
- Records that can be separated out from all other records in a reasonable time, or marked so they are visually identifiable — the red C convention. It is a formal DEA standard, not a figure of speech.
- RecallPatient Safety & Quality Assurance
- Removal of a defective or unsafe drug product from the market.
- Recall depthFederal Requirements
- How far down the distribution chain a recall reaches — wholesaler, retail, or consumer level. A consumer-level recall means the pharmacy notifies the patients who received the affected lot.
- ReconstitutionMedications
- Adding a diluent to a powder to make a liquid, often refrigerated after mixing.
- Red flag (dispensing)Federal Requirements
- Warning sign of possible diversion or forgery requiring pharmacist review before dispensing.
- Refill too soonOrder Entry & Processing
- Rejection when a refill is requested before allowed date.
- REMSFederal Requirements
- An FDA safety program managing a drug's serious risks
- Return to stockOrder Entry & Processing
- Putting a prescription that was never picked up back into inventory and reversing the claim. Only possible because the product never left your control.
- Reverse distributorOrder Entry & Processing
- A licensed company that takes expired or unsaleable stock from a pharmacy and processes it for manufacturer credit and destruction.
- Reye syndromeMedications
- Rare but severe brain and liver injury linked to salicylates given during a viral illness in children and teenagers. It is the reason aspirin is avoided in that age group.
- Root cause analysisPatient Safety & Quality Assurance
- Structured investigation to find the underlying cause of a serious error.
- Safety Data SheetPatient Safety & Quality Assurance
- Document detailing a chemical's hazards, handling, and emergency measures.
- SalicylateMedications
- The aspirin family. It matters beyond aspirin itself: bismuth subsalicylate is a hidden salicylate, which is why it is avoided in a child or teenager with a viral illness because of Reye syndrome.
- Schedule IFederal Requirements
- High abuse potential and no accepted medical use
- Schedule IIFederal Requirements
- High-abuse drugs with accepted medical use; no refills allowed (e.g., oxycodone, Adderall).
- Schedule II refillsFederal Requirements
- Not allowed; a new prescription is required
- Schedule IIIFederal Requirements
- Moderate abuse potential; may be refilled up to 5 times within 6 months.
- Schedule III-IV refillsFederal Requirements
- Up to 5 times within 6 months
- Schedule IVFederal Requirements
- Low abuse potential (e.g., alprazolam); refillable up to 5 times in 6 months.
- Schedule VFederal Requirements
- Lowest abuse potential; some may be sold OTC with restrictions where state law allows.
- Secure and Responsible Drug Disposal ActFederal Requirements
- The 2010 law that let patients hand unused controlled substances back to authorized collectors. Before it, there was no lawful way to return them to a pharmacy.
- Sentinel eventPatient Safety & Quality Assurance
- An unexpected event causing death or serious harm
- Separate CII recordsFederal Requirements
- Schedule II records must be kept separate from all other pharmacy records.
- Sewer banFederal Requirements
- The EPA prohibition on discharging hazardous waste pharmaceuticals into a sewer system that runs to a public treatment works. No flushing, no pouring down the drain.
- Short-datingOrder Entry & Processing
- Stock close enough to its expiration date that it should be pulled and credited now, while the wholesaler still accepts it.
- SigOrder Entry & Processing
- Directions for how the patient takes the drug
- SLMedications
- Sublingual; medication dissolved under the tongue for fast absorption.
- SL nitroglycerinFederal Requirements
- PPPA-exempt from child-resistant packaging
- Spacer (valved holding chamber)Order Entry & Processing
- A chamber attached to a metered-dose inhaler that holds the puff, so the patient does not have to press and inhale at the same instant. Also cuts the drug left in the mouth.
- Specific gravityOrder Entry & Processing
- Ratio of a substance's weight to equal volume of water.
- SSRIMedications
- Antidepressant that raises serotonin; e.g., sertraline, fluoxetine.
- statOrder Entry & Processing
- Immediately, right away
- Sterile techniquePatient Safety & Quality Assurance
- Practices that keep compounded sterile products free of contamination.
- SublingualMedications
- Under the tongue. The tablet or film dissolves there and absorbs straight into the bloodstream, bypassing the stomach and first-pass metabolism — which is why swallowing it wastes most of the dose.
- SUBQOrder Entry & Processing
- Subcutaneous (under the skin)
- SubQ / SCMedications
- Subcutaneous; injection into fatty tissue under the skin.
- SubscriptionOrder Entry & Processing
- Prescriber's directions to the pharmacist for preparing/dispensing.
- SulfonylureaMedications
- A diabetes drug class ending in -ide (glipizide, glyburide) that makes the pancreas release insulin. Because it works whether or not you have eaten, it can cause hypoglycemia — unlike metformin.
- SuperscriptionOrder Entry & Processing
- The Rx symbol beginning the prescription order.
- suppOrder Entry & Processing
- Suppository dosage form.
- SuppositoryMedications
- Solid dosage form inserted rectally or vaginally that melts to release drug.
- SuspensionMedications
- Liquid dosage form with undissolved particles; shake well before use.
- SynthroidMedications
- Brand name for levothyroxine (thyroid hormone)
- tabOrder Entry & Processing
- Tablet dosage form.
- Tall man letteringPatient Safety & Quality Assurance
- Mixed-case letters that tell look-alike drug names apart
- Tamper-evidentPatient Safety & Quality Assurance
- Packaging that visibly shows if it has been opened. Federal rules require it on most OTC products. A broken seal means the product does not go on the shelf.
- Temperature excursionMedications
- When stored product goes outside its labeled temperature range. Label it DO NOT USE, keep it separate, and contact the manufacturer or program — do not discard it and do not dispense it.
- The Joint CommissionPatient Safety & Quality Assurance
- Organization that accredits and sets safety standards for healthcare facilities.
- Therapeutic duplicationMedications
- Two drugs on one profile doing the same job — same class, the same drug under brand and generic, a combination product plus one of its own ingredients, or an OTC on top of a prescription. Flag it for the pharmacist.
- Therapeutic substitutionPatient Safety & Quality Assurance
- Dispensing a chemically different drug in the same class as the one prescribed (not just a generic of it). State generic-substitution laws do NOT cover this — it needs prescriber authorization, or in a hospital a P&T-approved interchange protocol.
- TIDOrder Entry & Processing
- Three times daily
- TopicalMedications
- Applied to skin or mucous membranes for local effect.
- Toprol-XLMedications
- Brand name for metoprolol, a beta blocker
- Trailing zeroPatient Safety & Quality Assurance
- Avoid 5.0 mg (reads as 50); write 5 mg
- Transaction history (T3)Federal Requirements
- DSCSA documentation of ownership: transaction information, history, and statement.
- TranscriptionOrder Entry & Processing
- Converting a prescriber's order into an accurate, fillable pharmacy record.
- TransdermalMedications
- Delivered through the skin via a patch for slow systemic absorption.
- TriturationOrder Entry & Processing
- Reducing particle size by grinding with a mortar and pestle.
- TrocheMedications
- A lozenge that dissolves slowly in the mouth to treat the mouth and throat locally rather than being swallowed.
- TrOOPOrder Entry & Processing
- True Out-Of-Pocket: the running total a Medicare Part D patient has actually paid, which is what moves them through the benefit phases.
- Tuberculin syringeOrder Entry & Processing
- A 1 mL syringe with fine graduations, used for very small volumes. It is marked in millilitres, not insulin units.
- Two patient identifiersPatient Safety & Quality Assurance
- Using two unique identifiers, such as name and date of birth, before dispensing.
- Two-year record retentionFederal Requirements
- Federal law requires controlled-substance records be kept at least two years.
- U-100 / U-500Medications
- Insulin concentrations. U-100 is 100 units per mL and is the standard; U-500 is five times as concentrated and is a high-alert product precisely because a U-100 syringe would measure it wrongly.
- U&COrder Entry & Processing
- Usual and Customary — what your pharmacy charges a cash-paying customer for a prescription. Plans generally pay the lower of their rate or your U&C.
- UDOrder Entry & Processing
- Ut dictum, meaning "as directed."
- ungOrder Entry & Processing
- Ointment (unguentum).
- USP <795>Patient Safety & Quality Assurance
- Standards for nonsterile compounding
- USP <797>Patient Safety & Quality Assurance
- Standards for sterile compounding
- USP <800>Patient Safety & Quality Assurance
- Standards for handling hazardous drugs
- USP coolPatient Safety & Quality Assurance
- 8 to 15 degrees C — a storage range distinct from refrigeration (2-8) and controlled room temperature (20-25).
- VAERSPatient Safety & Quality Assurance
- Vaccine Adverse Event Reporting System for reporting problems after vaccination.
- Vented administration setOrder Entry & Processing
- An IV set with a filtered air vent, used with rigid GLASS containers so air can replace the fluid draining out. Collapsible plastic bags do not need one.
- VerificationOrder Entry & Processing
- Pharmacist's final check of the filled prescription before dispensing.
- Verify DEA checksumFederal Requirements
- Add digits 1,3,5; add digits 2,4,6 times two; sum's last digit equals digit seven.
- VICPPatient Safety & Quality Assurance
- The National Vaccine Injury Compensation Program, run by HRSA. It is the separate no-fault program that pays compensation for vaccine injuries. VAERS only collects reports; it never determines causation and never pays anything.
- WACOrder Entry & Processing
- Wholesale Acquisition Cost — the manufacturer’s list price to the wholesaler, before discounts. Not what the pharmacy actually paid.
- Will-callOrder Entry & Processing
- Storage area holding filled prescriptions awaiting patient pickup.
- XanaxMedications
- Brand name for alprazolam, a Schedule IV benzodiazepine
- ZoloftMedications
- Brand name for sertraline, an SSRI antidepressant