Controlled Substances
Drug Safety
Mailing Regulations
Patient Package Inserts
Prescription Labels
100
CLASS II SUBSTANCES ARE AT A HIGH RISK OF ____ AND _____?
ABUSE AND DEPENDENCE
100
WHAT FEDERAL AGENCY APPROVES DRUGS AS SAFE AND EFFECTIVE
THE FOOD AND DRUG ADMINISTRATION (FDA)
100
WHAT IS THE ACT THAT REQUIRED CHILDPROOF PACKAGING ON MOST DRUGS DISPENSE IN A PHARMACY?
POISON PREVENTION PACKAGING ACT OF 1970
100
TRUE OR FALSE: HCP'S ARE HEALTHCARE PROVIDERS
TRUE
100
WHAT IS MISBRANDING?
NO LABEL, FALSE LABELING, LABEL LACKS NAME, MANUFACTURER, DISTRIBUTOR AND/OR LACK ACCURATE QUANTITY OF CONTENTS
200
THERE ARE HOW MANY CONTROLLED SUBSTANCE SCHEDULES?
FIVE
200
THE EXTENT IN WHICH A DRUG WORKS UNDER IDEAL CIRCUMSTANCES
EFFICACY
200
WHO'S RESPONSIBLE FOR KNOWING THE MAILABILITY OF SUBSTANCES SUCH AS IT BEING FLAMMABLE OR TOXIC?
THE MAILERS
200
WHICH IS THE MOST SERIOUS MEDICATION WARNING LABEL REQUIRED BY THE FDA?
BLACK BOX WARNING
200
THE ADDITIONAL WARNING LABELS THAT ARE PLACED WHEN A MEDICATION IS BEING FILLED ARE CALLED...
AUXILIARY LABELS
300
HOW LONG DOES THE FEDERAL LAW REQUIRE PHARMACIES TO KEEP C-II RECORDS FOR?
TWO YEARS
300
THE INHERENT CAPABILITY OF AN INTERVENTION TO CAUSE HARM OR A POTENTIAL SOURCE OF HARM
A HAZARD
300
THE ACT THAT PROHIBITS INTERSTATE TRANSPORTATION OR SALE OF ADULTERATED AND MISBRANDED FOOD OR DRUGS
PURE FOOD AND DRUG ACT OF 1906
300
WHAT INFO DOES THE CONTRAINDICATION SECTION OF A PACKAGE INSERT CONTAIN?
IT LISTS SITUATIONS IN WHICH MEDICATIONS SHOULD NOT BE USED
300
WHAT IS THE FEDERAL LAW THAT PROHIBITS THE TRANSFER OF A DRUG TO ANY PERSON OTHER THAN THE PATIENT FOR WHOM IT WAS PRESCRIBED?
THE CONTROLLED SUBSTANCE TRANSFER WARNING
400
THE LEVEL OF CONTROL OF A DRUG DETERMINES...
ITS SCHEDULE
400
MISTAKES IN PRESCRIBING, TRANSCRIBING, DISPENSING, ADMINISTERING AND MONITORING OF MEDICATIONS ARE REFERED TO AS...
MEDICATION ERROR
400
WHAT NUMBER OR CODE IS USED ON PRESCRIPTION LABELING TO IDENTIFY THE MANUFACTURER, DRUG AND SIZE/QUANTITY
NATIONAL DRUG CODE (NDC)
400
WHAT DOES THE MECHANISM OF ACTION DO?
IT DESCRIBES HOW A MEDICATION WORKS
400
WHAT IS THE PRIMARY PURPOSE OF PRESCRIPTION DRUG LABELING?
TO GIVE HEALTHCARE PROFESSIONALS THE INFO THEY NEED TO PRESCRIBE MEDICATIONS APPROPRIATELY
500
THE FEDERAL LAW THAT REGULATES THE MANUFACTORING, DISTRIBUTION, STORAGE, DISPENSING AND RECORD KEEPING OF CONTROLLED SUBSTANCES IS?
CONTROLLED SUBSTANCES ACT
500
IN PHARMACEUTICAL PRODUCTS, THE COLLECTION, DETECTION, ASSESSMENT, MONITORING AND PREVENTION OF ADVERSE EFFECTS ARE REFERED TO AS...
PHARMACOVIGILANCE
500
WHICH ACT REQUIRES THAT ALL MEDICAL DEVICES BE TRACKED AND RECORDS BE MAINTAINED FOR DURABLE MEDICAL EQUIPMENT.
THE FDA SAFE MEDICAL DEVICES ACT OF 1990
500
WHAT TYPE OF INFO DOES THE PRECAUTION SECTION GIVE US?
IT EXPLAINS HOW TO USE THE MEDICATION SAFELY
500
CONTROLLED SUBSTANCE LABELS FOR SCHEDULES II, III AND IV MUST CARRY AN AUXILIARY LABEL STATING...
CAUTION: FEDERAL LAW PROHIBITS THE TRANSFER OF THIS DRUG TO ANY PERSON OTHER THAN THE PATIENT FOR WHOM IT WAS PRESCRIBED
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