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When to wash hands
Before and after patient contact, after touching contaminated surfaces, before preparing any medication, after removing gloves
Proper Hand Washing Technique
Wet hands , soap, scrub 20 seconds, rinse, dry
Alcohol based hand rub (ABHR)
Acceptable alternative UNLESS hands are visibly soiled or after C.diff exposure (soap and water required for C.diff)
Gloves
Always when handling medications, hazardous drugs, or patient samples
Gown/Lab coat
Sterile compounding, hazardous drugs handling (chemo)
Mask/Respirator
Sterile compounding, hazardous drug preparation (N95 for some)
Eye protection/ Face shield
Hazardous drug compounding, splash risk
Hair covers/Shoe covers
Required in clean room/sterile compounding
Counting trays
Clean with 70% isopropyl alcohol (IPA) between patients; dedicated trays for penicillin based drugs (allergy risk from residue)
Countertops
Disinfect regularly with approved solutions
Laminar flow hood (sterile compounding)
Clean with 70% IPA before use, and every 30 min during use and after spills
Hazardous drug spills
Use a hazardous spill kit; double glove; seal waste in appropriate containers
ISO 5
Where actual drug preparation happens (inside hood)
ISO 5
Buffer area/cleanroom around the hood
ISO 8
Ante-area (where you gown up before entering)
Wrong Drug
Incorrect medication Dispensed
Wrong Dose
Incorrect strength given
Wrong Patient
Medication given to the wrong person
Wrong Route
Incorrect administration route
Wrong Quantity
Incorrect amount dispensed
Wrong Time
Medication given at wrong time
Omission Error
Dose not given/missed
Unauthorized Drug
Drug dispensed without valid order
QD/Daily
Once daily
BID
Twice daily
TID
Three times daily
QID
Four times daily
Q4H
Every 4 hours
Q6H
Every 6 hours
Q8H
Every 8 hours
Q12H
Every 12 hours
PRN
As needed
AC
Before meals
PC
After meals
HS
At bedtime
Drug Utilization Review (DUR)
Computer flags a drug interaction, allergy, or duplication → stop and alert pharmacist
Adverse Drug Event (ADE)
Patient calls saying they had a bad reaction to their medication
OTC Recommendation
Patient asks which OTC product to use for their symptoms → pharmacist only
Therapeutic substitution
Prescriber asks for a different drug in same class (e.g., brand → generic, or switching statin) → pharmacist approval needed
Drug misuse/abuse concerns
Patient seems to be misusing medications, early refills on controlled substances, multiple prescribers
Adherence issues
Patient hasn't refilled a critical medication in months (e.g., blood pressure, insulin)
Post-immunization care
Patient has adverse reaction after vaccine given in pharmacy
Allergy concerns
Prescription written for drug the patient is allergic to
Unclear/ambiguous prescription
Illegible writing, missing dose or directions
Drug-disease concern
Prescribed drug appears contraindicated for a known condition in patient profile
Prospective DUR
BEFORE dispensing (most common)
Generic Substitution
Same drug, different manufacturer (brand → generic)
Therapeutic Substitution
Different drug, same class (e.g., omeprazole → pantoprazole)
Concurrent DUR
While patient is in hospital, during treatment
Retrospective DUR
AFTER dispensing (look back at records)
Insulin (High Alert Meds)
Wrong type or dose → hypoglycemia, death
Anticoagulants (warfarin, heparin, apixaban) (High Alert Meds)
Too much → major bleeding; too little → clot/stroke
Opioids (morphine, fentanyl, oxycodone) (High Alert Meds)
Respiratory depression, death at high doses
Concentrated Electrolytes (KCI, NaCl 3%, MgSO4) (High Alert Meds)
IV bolus can be fatal — must be diluted
Chemotherapy Agents (High Alert Meds)
Narrow therapeutic index; toxic to healthy cells
Neuromuscular Blocking Agents (succinylcholine) (High Alert Meds)
Paralyzes patient — must have airway support ready
Methotrexate (oral) (High Alert Meds)
Weekly dosing often confused with daily → toxicity/death
Hypertonic Saline (NaCl 3%) (High Alert Meds)
Rapid infusion → brain damage
IV digoxin (High Alert Meds)
Narrow therapeutic index; toxicity risk
Why is using “U” for units dangerous?
It looks like “0” or “4,” which can cause a serious insulin overdose. Write “units”.
Why should “MS,” “MSO₄,” and “MgSO₄” be avoided?
They can be confused (morphine vs. magnesium sulfate). Write the full drug name.
Why is “D/C” considered unsafe?
It can mean discontinue or discharge. Always spell out the intended meaning.
Why should “cc” not be used?
It can look like “00” in handwriting. Use mL (milliliters) instead.
Why is “µg” risky?
The “µ” can look like “m,” causing a 1000× dosing error. Write mcg (micrograms).
Why is “QOD” dangerous?
It can be misread as “QD” or “QID.” Write “every other day.”
Why is “QD” unsafe?
It can be confused with “QID” (4 times daily). Write “daily.”
Why should “IU” not be used?
It can be mistaken for “IV” or “10.” Write “international units”.
Barcode scanning
Scan drug AND patient wristband before dispensing
Separating inventory
Store LASA drugs in different locations; use physical barriers or different shelves
Auxiliary labels
"Shake well," "For the eye," "Take with food" — reduce administration errors
Double-checking
Pharmacist verifies tech's work before dispensing (required by law)
Computer alerts/DUR
Electronic systems flag interactions, duplications, allergies
Patient counseling
Pharmacist must offer counseling for new prescriptions (OBRA '90)
What is MedWatch (FDA) used for? Who can report?
Reports adverse drug reactions, product problems, and medication errors for marketed drugs. Reported by healthcare providers, patients, and manufacturers.
What is VAERS? Who can report?
Vaccine Adverse Event Reporting System — used to report adverse reactions after vaccines. Anyone can report (providers are required, public is encouraged).
What is ISMP used for? Who reports to it?
Voluntary, confidential medication error reporting system that helps create national safety alerts. Reported by healthcare professionals.
What do State Boards of Pharmacy handle? Who reports?
Handle disciplinary issues, license violations, and dispensing errors. Reports can come from pharmacies and consumers.
Medication Error
Any preventable event that cause or lead to inappropriate medication use or patient harm
Adverse Drug Event (ADE)
Harm caused by a drug whether or not it was an error (includes side effects and allergic reactions)
Near Miss (close call)
An error that was caught BEFORE reaching the patient.. still must be documented and reported internally
Sentinel Event
Unexpected death or serious physical/psychological harm.. requires immediate root cause analysis
Class I Recall
Most serious — product likely to cause serious harm or death (e.g., contamination, wrong drug). Remove from shelves IMMEDIATELY.
Class II Recall
May cause temporary or reversible harm. Respond promptly.
Class III Recall
Unlikely to cause harm but violates FDA regulations (e.g., labeling issue).