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pharmacy laws and their definitions

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law
definition
Pure food and drug act of 1906   prohibited foreign and interstate traffic in adulterated and misbranded food and drugs; required that the active ingredients be listed on the label and drugs could not fall below purity levels established by the USP or national formulary  
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Harrison narcotic act of 1914   first use of federal criminal law in the US to deal with the non medical use of drugs  
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Food Drug and Cosmetic act of 1938   clearly defined adulteration and misbranding of drugs and food products  
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Comprehensive Drug Abuse Prevention and Control act of 1938   required that all narcotics be labeled "warning; may be habit forming"  
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Durham-Humphrey Act of 1950   defining which drugs can and cannot be dispensed without a valid prescription and must include federal legend :"caution: federal law prohibits use without prescription" or "rx only" on the label and allows phone prescriptions  
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Kefauver-Harris Act of 1950   mandated that manufacturer must provide proof of safety and effectiveness before marketing new drugs.  
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Social Security Act of 1965   established Medicare  
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Fair Packaging and Labeling Act of 1966   all consumer products must be honestly and informatively labeled  
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Comprehensive Drug Abuse Prevention and Control Act of 1970 (controlled Substance Act)   created under the DEA; controlled substances were placed in one of 5 categories and must be labeled : "Warning: May be habit forming"  
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Occupational Safety and Health Act of 1970 (OSHA)   ensured a safe and healthful workplace for employees; created SDS  
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Poison Prevention Act of 1970   child resistant caps to reduce poisoning in children and permits certain meds not to be dispensed in child resistant containers  
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Consumer Products Safety Commission   enforces the Poison Prevention Act  
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Drug Listing Act of 1972   created the National Drug Code: 11 digit number that identifies the manufacturer, product, and package size  
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Orphan Drug Act of 1983   provides incentives to promote research, approval and marketing of drugs needed for treatment of rare diseases by streamlining the drug development process  
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Drug Price Competition and Patent Term Restoration Act of 1984 (Hatch-Waxman)   allows for extension of drug patents and quicker introduction of lower-cost generics  
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Omnibus Budget Reconciliation Act of 1987 (OBRA87)   establishes revisions to Medicare and Medicaid regarding long term care facilities including: meds must be labeled' pt regimen must be free of unnecessary meds, antipsychotic meds' consultant RPH, and routine and emergency meds provided  
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Prescription Drug Marketing Act of 1987   prohibits re-importation of a drug by anyone but the manufacturer  
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Omnibus Budget Reconciliation Act of 1990 (OBRA90)   requires all pharmacies to maintain profiles on patients (DUE/DUR)  
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Dietary Supplemental Health and Education Act of 1994   required all herbal products to be labeled as a dietary supplement  
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Health Insurance Portability and Accountability Act 1996 (HIPAA 96)   was concerned with insurance reform, patient confidentiality, and security of computer system; PHI-PROTECTED HEALTH INFORMATION  
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Medicare Drug Improvement and Modernization Act of 2003   provided voluntary prescription drug benefits to Medicare beneficiaries, added for seniors, lowered reimbursement rates for Medicare payment for med equip., discount card program  
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MTM   Medication Therapy Management and tax free savings  
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Anabolic Steroid Control Act of 2004   provided requirements for handling substances defined as anabolic steroids (schedule 3 drugs)  
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Isotretinoin Safety and Risk Management Act of 2004   the rx must be hand written and dispensed within 7 days after being written and limits the dispensing to a 30 day supply with no refills: refills can not be called into the pharmacy  
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Combat Methamphetamine Epidemic Act of 2005   the maximum allowed amount of pseudoephedrine that may be purchased in a single day is 3.6 g; maximum in a 30 day period is 9g. must be locked and id required for purchase  
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Patient Protection and Affordable Care Act of 2010   health care reform for the uninsured; reduced the amount that may be set aside for a flexible spending account  
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Prescription Drug Equity Law   assured equitable treatment in health care coverage of prescription drugs under group health plans , health insurance coverage, medicare and Medicaid, medigap, and health plans under the federal employees health benefits program  
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Freedom Choice Law   permits an enrollee to obtain reimbursable health care services from any qualified provider even if they aren't signed with the manage care plan  
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Americans With Disabilities Act   prohibits discrimination against individuals with physical, mental, and emotional disabilities  
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FDA   responsible for reviewing and approving all investigational new drug apps  
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Created by: tconway33
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