Controlled Substances Questions. All e-prescriptions must go through the Surescripts exchange. (Schedules III-V). The Schedule 3 Narcotics List does not contain any illegal drugs and mainly contains steroids and diet pills. While lots of money flows through the illegal drug market, the market for licensed pharmaceuticals carries just as much potential for profit. Practitioners and pharmacies. Prescriptions for Schedule 3 drugs can only be written. Labeling that is false or misleading. Packaging that does not bear a label containing the name of business of the maufacturer, packer, or distributer or an accurate quantity of contents or is not conspicuously and clearly labeled with information required. Failure to bear the established name of drug, and in the case it carries two or more active ingredients, the amount of alcohol and also including whether active or not. The established names of other substances described in the act. Failure to label with adequate instructions or warnings. Products that are dangerous to health when used in dosage or manner or duration perscribed, recommended or suggested in the labeling. The transfer of controlled substance prescriptions ______ permitted. Transfer must be communicated between two licensed ________. The transferring pharmacist is responsible for writing _____ on the face of the transferred prescription; writing the name, address, and DEA number of the receiving pharmacy on the back side of the prescription; and recording the _____ of transfer and the name of the pharmacist _________ the prescription. The receiving pharmacist is responsible for writing the word ________ on the face of the prescription and recording the date of ______ of the original prescription, _______ number of refills authorized, date of original dispensing, number of valid refills ______ and location of previous refills, the _______ pharmacies name, address, DEA number, and prescription number, name of the pharmacist transferring prescription. The original and transfer prescription must be kept for ___ years from the date of ________. Established extensive revisions to Medicare and Medicaid Conditions of Participation regarding long-term care facilities and pharmacy. Requires manufacturers to provide the lowest prices to any customer or Medicaid patient by rebating each state Medicaid agency the difference between its average price and its lowest price. Requires that an 'offer to counsel' is made to every patient and drug utilization review is performed for every patient; failure to do so may result inloss of Medicare funds. Authorizes government sponsored demonstration projects relating to the provision of pharmaceutical care; patient profiles are to be maintained for all patients. The manufacturers of supplements are allowed to make claims with regard to general health promotion, but not disease claims. Herbal products must meet the following guidelines: be labeled as a dietary supplement, have labeling that identifies all ingredients by name, have labeling that lists the quantity of each ingredient, have packaging that identifies the plant and plant part from which the ingredient is derived, comply with standards set by an official compendium,and meet the quality, purity, and compositional specification. Put in place to improve the portability and continuity of health coverage in the group and individual markets; combat waste, fraud, and abuse in health insurance and health care delivery; promote the use of medical savings accounts; improve access to long-term care services and coverage; and simplify the administration of health insurance. Requires that health care providers ensure patient confidentiality be maintained. Requires that patients be informed of how their protected information will be used. Protected information includes: past, present, and future health information; past, present, and future payments for health services; specific care a patient has, is, or will be receiving; any information that can identify the patient; any information that someone could reasonably use to identify the patient. There are 2 parts to HIPAA: Title I: Insurance Reform and Title II: Administrative Simplification. Accutane (Isotretinoin) is a powerful medication used to treat acne. The medication has been found to cause severe birth defects, induce spontaneous abortions, and produce adverse psychiatric effects including, depression, psychosis, suicidal ideation, suicide attempts, and suicide. Amended the Controlled Substances Act and replaced the existing definition of anabolic steroid. The new definition altered the basis for all future administrative scheduling actions relating to the control of anabolic steroids as Schedule III medications by eliminating the requirement to prove muscle growth. This should be your intention too, as a user, to fully evaluate 3ds max 2014 without restrictions and then decide. Our intentions are not to harm 3ds software company but to give the possibility to those who can not pay for any piece of software out there. If you are keeping the software and want to use it longer than its trial time, we strongly encourage you purchasing the license key from 3ds official website. 3d max 2014 torrent. Our releases are to prove that we can! This act increased the number of anabolic steroids to 59 drugs. Amendment provided the requirements for handling substances defined as anabolic steroids to include registration, security, labeling and packaging, inventory, record maintenance, prescriptions, disposal, importation and exportation, and criminal liability. Provides for a voluntary prescription drug benefit to Medicare beneficiaries; adds preventative medical benefits to senior citizens; lowers the reimbursement rates for Medicare payment for durable medical equipment; created a national competitive bidding program for durable medical equipment in 2007; changed the way Medicare pays for outpatient Part B drugs; allowed for a voluntary Medicare-approved discount card program in 2004; Medicare Part D prescription plan allows beneficiaries to enroll in either regional or national based insurance plans. Federal law that placed ephedrine, pseudoephedrine, and phenylpropanolamine in the Controlled Substances Act category 'scheduled listed chemical products'. Products containing these drugs are subject to sales restrictions, storage requirements, and record-keeping requirements. The act specifies a 3.6 g/ day based product sales limit, a 9 g/ 30 day base product sales limit, a blister package requirement, and mail order restrictions. Logbook requirements have been implemented and require products by name, quantity sold, names and addresses of purchasers, and date and time of sales. In April of 2008, physicians were required to adhere to the requirements of the Medicaid Tamper-Resistant Prescription Act. Applies to all handwritten prescriptions for covered outpatient drugs; drugs that are transmitted from the prescriber to the pharmacy verbally, by fax, or through e-prescribing are not affected by this legislation. Applies wherever Medicaid pays any portion of the cost of a prescription. Kentucky Scheduled Drugs Iii Through V Prescriptions 2017A tamper-resistant prescription pad must inclide one of the following: one or more industry recognized features designed to prevent unauthorized copying of a prescription form; one or more features designed to prevent the erasure or modification of information written on a prescription; or one or more features designed to prevent the use of counterfeit prescription forms. As of October 2008, all three of these items must be included on the prescription pad to be considered tamper resistant. Designed to cut down on infections transmitted to patients through pharmaceutical products and to protect staff working in pharmacies in the course of their exposure to pharmaceuticals. Addresses the following: Microbial contamination risk levels; personnel training and evaluation in aseptic manipulation skills; clean rooms to include ante-rooms, air classification, physical characteristics of the construction, and gowning procedures; barrier isolaters; formalized quality assurance program; minimum requirements for validation; cleaning and sanitizing workspaces; environmental monitoring; and verification of automated compounding devices for nutrition compounding. Formerly the Joint Commission on Accreditation of Healthcare Organizations (JCAHO).
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |