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Comprehensive vocabulary flashcards covering PTCB pharmacy math, sig codes, generic drug stems, federal pharmacy laws, and drug interaction/safety concepts.
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1 tsp
5mL
1 tbsp
15mL
1 fl oz
30mL
1 cup
8oz=240mL
1 pint
16oz=480mL
1 quart
32oz=960mL
1 gallon
128oz=3840mL
2.2 lb
1kg
1 in
2.54cm
Fahrenheit to Celsius Formula
∘C=(∘F−32)×95
Celsius to Fahrenheit Formula
∘F=(∘C×59)+32
Ratio Strength 1:1000
1g/1000mL=1mg/mL
King Henry Died By Drinking Chocolate Milk
Memory aid for metric units (kilo, hecto, deka, base, deci, centi, milli)
bid
Twice daily
tid
Three times daily
qid
Four times daily
ac
Before meals
pc
After meals
po
By mouth
SL
Sublingual
qhs
Every night at bedtime
prn
As needed
od
Right eye
os
Left eye
ou
Both eyes
ad
Right ear
as
Left ear
au
Both ears
DAW
Dispense as written
qs
Quantity sufficient
-pril
Angiotensin-converting enzyme (ACE) inhibitors; used as antihypertensives
-sartan
Angiotensin II receptor blockers (ARBs); used as antihypertensives
-olol
Beta blockers; used for antihypertension or rate control
-statin
HMG-CoA reductase inhibitors; used as antihyperlipidemics
-triptan
5-HT1B/1D agonists; used for migraine treatment
-afil
Phosphodiesterase-5 (PDE-5) inhibitors; used for erectile dysfunction
-prazole
Proton pump inhibitors (PPIs); used for GERD/acid suppression
-azole
Azole antifungals
-zepam / -zolam
Benzodiazepines; used as anxiolytics or sedatives
-setron
5-HT3 receptor antagonists; used as antiemetics
-dronate
Bisphosphonates; used for osteoporosis treatment
Schedule II (C-II)
High abuse potential with accepted medical use; strictly controlled and allows no refills
Schedule III-V Refill Rule
Up to 5 refills within 6 months federally
Inhibitor
Blocks enzyme activity so substrate levels increase and toxicity risk rises
Inducer
Increases enzyme activity so substrate levels fall and treatment failure risk rises
CYP3A4
A major enzyme that metabolizes many drugs and has the most clinical interactions
High-Risk Teratogens
ACE inhibitors, ARBs, Warfarin, Methotrexate, Valproate, Isotretinoin, Finasteride, Statins, Spironolactone, and Raloxifene
Pure Food and Drug Act (1906)
The first federal law regulating drugs; focused on accurate labeling and purity
Food, Drug, and Cosmetic Act (1938)
Required drugs to be safe and prohibited adulteration and misbranding
Durham-Humphrey Amendment (1951)
Separated drugs into Prescription (Rx) and OTC categories; required the federal legend on labels
Kefauver-Harris Amendment (1962)
Required proof of efficacy (drugs must be safe and effective) and mandated Good Manufacturing Practices (GMPs)
Controlled Substances Act (1970)
Created drug schedules (I-V) and the DEA to regulate drugs with abuse potential
Poison Prevention Packaging Act (1970)
Required child-resistant packaging for most potentially harmful drugs, with exceptions like Nitroglycerin
Drug Listing Act (1972)
Established the National Drug Code (NDC) system
NDC Format (5-4-2)
A 10 or 11 digit code where the first 5 digits represent the manufacturer, the next 4 the product code, and the last 2 the package size
Orphan Drug Act (1983)
Provides incentives, such as 7-year market exclusivity, to develop drugs for rare diseases affecting fewer than 200,000 people
OBRA '90
Omnibus Budget Reconciliation Act of 1990; established the requirement for pharmacists to offer counseling to patients
HIPAA (1996)
Health Insurance Portability and Accountability Act; protects patient privacy and Protected Health Information (PHI)
Combat Methamphetamine Epidemic Act (2005)
Restricted sales of pseudoephedrine/ephedrine to behind the counter with record-keeping and quantity limits
CMEA Quantity Limits
3.6g/day and 9.0g/30days
Adulteration
Occurs when a drug is filthy, impure, or when its strength, quality, or purity differs from the label or standards
Misbranding
False or misleading labeling, or missing required warnings and information