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18 Cards in this Set
- Front
- Back
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-REQUIRED PHARMACIST TO ENGAGE IN DRUG UTILIZATION REVIEWS (DUR) -REQUIRED PHARMACISTS TO OFFER COUNSELING TO PATIENTS ABOUT THEIR PRESCRIPTIONS WITHOUT CHARGE |
OMNIBUS BUDGET RECONCILIATION ACT (OBRA) - 1990 |
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-REDEFINED ANABOLIC STEROIDS AS SCHEDULE III CONTROLLED SUBSTANCES |
ANABOLIC STEROID CONTROL ACT - 1990 |
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-PROHIBITED THE RE-IMPORTATION OF DRUGS TO THE UNITED STATES, EXCEPT BY THE MANUFACTURER |
PRESCRIPTION DRUG MARKETING ACT - 1987 |
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-STREAMLINED THE FDA APPROVAL PROCESS FOR MARKETING GENERIC DRUGS -EXTENDED THE TERM OF PATENTS FOR COMPANIES THAT DEVELOP NEW DRUGS |
DRUG PRICE COMPETITION & PATENT TERM RESTORATION ACT - 1984 |
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-PROVIDED TAX INCENTIVES FOR DEVELOPING & MARKETING DRUGS USED TO TREAT RARE CONDITIONS (ORPHAN DRUGS) -ESTABLISH LIFELONG EXCLUSIVE LICENSE TO MANUFACTURER THAT DEVELOPED AN ORPHAN DRUG |
ORPHAN DRUG ACT - 1983 |
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-REQUIRE NDC #'S BE ASSIGNED TO EVERY MARKETED DRUG |
DRUG LISTING ACT - 1972 |
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-REQUIRED CHILD-RESISTANT CONTAINERS FOR MOST PRESCRIPTION & OTC DRUGS TO PREVENT ACCIDENTAL INGESTION & POISONING |
POISON PREVENTION PACKAGING ACT - 1970 |
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-ESTABLISH THE FEDERAL AGENCY CALLED THE DEA -CLASSIFIED DRUGS THAT HAVE THE POTENTIAL FOR ABUSE &/OR ADDICTION INTO 5 CLASSES |
COMPREHENSIVE DRUG ABUSE PREVENTION & CONTROL ACT (CONTROLLED SUBSTANCE ACT) - 1970 |
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-REQUIRED THAT DRUGS BE NOT ONLY SAFE BUT EFFECTIVE AS WELL -REQUIRED THAT PHARMACEUTICAL MANUFACTURERS FILE AN INVESTIGATIONAL NEW DRUG APPLICATION (INDA) BEFORE STARTING CLINICAL TRIALS ON HUMAN SUBJECTS |
KEFAUVER-HARRIS AMENDMENT TO FDCA - 1962 |
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-DISTINGUISHED BETWEEN PRESCRIPTION & NON-PRESCRIPTION DRUGS -REQUIRED THAT ALL DRUG PRODUCTS HAVE ADEQUATE USAGE DIRECTIONS OR BEAR THE LEGEND "CAUTION: FEDERAL LAW PROHIBITS WITHOUT PRESCRIPTION" -ALLOWED VERBAL PRESCRIPTION & REFILL REQUEST TO PHARMACIES BY TELEPHONE |
DURHAM-HUMPHREY AMENDMENTS TO FDCA - 1951 |
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-CLEARLY DEFINED ADULTERATION & MISBRANDING -CREATED THE FEDERAL AGENCY CALLED THE FOOD & DRUG ADMINISTRATION (FDA) |
FOOD, DRUG, & COSMETIC ACT (FDCA) - 1938 |
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-FIRST LAW TO REGULATE THE DEVELOPMENT, COMPOUNDING, DISTRIBUTION, STORAGE, & DISPENSING OF DRUGS -NO FALSE OR MISLEADING INFO. ON LABEL ABOUT DRUG STRENGTH OR PURITY -NO INTERSTATE TRANSPORT OR SALE OF ADULTERATED OR MISBRANDED FOOD OR DRUGS |
PURE FOOD & DRUG ACT - 1906 |
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-RESTRICTED SALES OF OTC DRUGS USED IN THE MANUFACTURE OF METHAMPHETAMINE'S SUCH AS: PSEUDOEPHEDRINE, EPHEDRINE, & PHENYLPROPANOLAMINE |
COMBAT METHAMPHETAMINE EPIDEMIC ACT - 2005 |
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-CHANGED FEDERAL LEGEND TO "RX ONLY" -LEGALIZED COMPOUNDING |
FDA MODERNIZATION ACT - 2004 |
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-PROVIDED A VOLUNTARY PRESCRIPTION DRUG PLAN FOR MEDICARE PATIENTS, FOR ADDITIONAL COST -CREATED A TYPE OF HEALTH INSURANCE CALLED HEALTH SAVINGS ACCOUNTS |
MEDICARE MODERNIZATION ACT - 2003 |
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-ADDRESSED PATIENT PRIVACY CONCERNS -ALLOWED FOR EMPLOYEES TO MORE EASILY MOVE THEIR HEALTH INSURANCE FROM ONE JOB TO ANOTHER |
HEALTH INSURANCE PORTABILITY & ACCOUNTABILITY ACT (HIPAA) - 1996 |
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-TREATED HERBAL SUPPLEMENTS AS FOOD PRODUCTS, RATHER THAN DRUGS -PROHIBITED MANUFACTURERS OF HERBS & DIETARY SUPPLEMENTS FROM MAKING CLAIMS THAT THEIR PRODUCTS TREAT OR CURE ANY SPECIFIC DISEASE OR ILLNESS |
DIETARY SUPPLEMENT HEALTH & EDUCATION ACT (DSHEA) - 1994 |
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WHAT IS A DEA FORM 222 FOR? |
TO ORDER SCHEDULE 2 (CII) DRUGS |
