OR MPJE flashcards
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- Oregon Board of Pharmacy
- State agency that licenses pharmacies, pharmacists, technicians, and interns and enforces Oregon pharmacy laws and rules under OAR Chapter 855.
- Pharmacist-in-charge duties
- Oregon's PIC is responsible for ensuring the pharmacy complies with recordkeeping, security, personnel supervision, and reporting requirements and must notify the Board of changes.
- Oregon PDMP check
- Oregon requires pharmacists to consult the Prescription Drug Monitoring Program before dispensing opioids and other specified controlled substances, with documented exceptions.
- Oregon CE requirement
- Oregon pharmacists must complete continuing education, including pharmacy law and patient safety hours, and report it through the Board's approved system at renewal.
- Oregon immunization authority
- Oregon pharmacists and certified technicians may administer vaccines to specified age groups under protocol, with documentation and reporting to the state immunization registry.
- Oregon CDTM
- Collaborative drug therapy management agreements in Oregon allow pharmacists to manage drug therapy under a written protocol with a prescriber, within defined scope.
- Oregon prescription contents
- Oregon prescriptions must include prescriber name, drug name, strength, quantity, directions, date, and patient name; electronic prescribing is the default with limited exceptions.
- Oregon record retention
- Oregon pharmacies must maintain prescription and dispensing records for the period set by Board rule, generally at least two years, and make them readily retrievable.
- Oregon drug loss reporting
- Oregon requires pharmacies to report significant drug losses, thefts, and adverse events to the Board within specified timeframes and to maintain documentation.
- Oregon technician ratio
- Oregon Board rules set the maximum number of certified pharmacy technicians and interns a pharmacist may supervise, with requirements for certification and training.
- Oregon drug outlet registration
- Oregon requires pharmacies and drug outlets to register with the Board and comply with facility, security, and personnel standards set by rule.
- Oregon emergency contraception
- Oregon pharmacists may dispense emergency contraception and certain hormonal contraceptives under statewide protocol without a prescription, with documentation requirements.
- Oregon prescription transfer
- Oregon rules govern transfer of prescription information between pharmacies, requiring direct communication and documentation for controlled and non-controlled drugs.
- Oregon intern requirements
- Oregon pharmacy interns must be enrolled in an approved pharmacy program and practice under pharmacist supervision, with hours documented for licensure.
- Oregon labeling rules
- Oregon requires dispensing labels to include pharmacy name, prescription number, patient name, directions, drug name and strength, and cautions as specified by rule.
- Oregon patient counseling
- Oregon rules require pharmacists to offer patient counseling on new and refill prescriptions, with documentation when counseling is declined.
- DEA registration
- Practitioners must register with the DEA for each principal place of business; registration is separate from state licensure and generally requires a valid state license.
- Schedule II refills
- Schedule II prescriptions may not be refilled; emergency oral orders require a written prescription within 7 days, and partial fills are limited by DEA rules.
- Schedule III-V refills
- Schedule III-V prescriptions may be refilled up to 5 times within 6 months of the date written unless the prescriber specifies otherwise.
- CSA schedules
- The Controlled Substances Act places drugs into Schedules I-V based on abuse potential and medical use; Schedule I has no accepted medical use.
- PPPA child-resistant packaging
- The Poison Prevention Packaging Act requires child-resistant packaging for most oral prescription drugs, with exceptions for certain drugs and patient-requested non-CR packaging.
- HIPAA privacy rule
- HIPAA protects individually identifiable health information and requires pharmacies to implement safeguards, business associate agreements, and breach notification procedures.
- REMS requirements
- Risk Evaluation and Mitigation Strategies impose restrictions such as restricted distribution, patient registries, and counseling requirements for certain high-risk drugs.
- CMEA pseudoephedrine log
- The Combat Methamphetamine Epidemic Act requires pharmacies to log ephedrine/pseudoephedrine sales, verify purchaser identity, and enforce daily and monthly purchase limits.
- Biennial inventory
- DEA registrants must take a biennial inventory of controlled substances, keep records for at least 2 years, and make them readily retrievable for inspection.
- FDA NDA/ANDA
- Prescription drugs require FDA approval through a New Drug Application or Abbreviated New Drug Application before marketing, with labeling and manufacturing standards.
- DEA Form 222
- DEA Form 222 is used to order Schedule I and II controlled substances; it must be completed accurately and retained as part of required records.
- Controlled substance theft reporting
- Registrants must notify DEA of significant theft or loss of controlled substances using DEA Form 106 and maintain records of the event.
- Prescription validity
- A valid prescription must be issued for a legitimate medical purpose by a practitioner acting in the usual course of professional practice.
- Electronic prescriptions
- Federal rules allow electronic prescribing of controlled substances with DEA-compliant systems; Schedule II-V e-prescriptions require identity proofing and audit trails.
- Medicare Part D coverage
- Medicare Part D provides outpatient prescription drug coverage through private plans, with formulary rules, coverage gaps, and pharmacy network requirements.
- DEA registration renewal
- DEA registrations must be renewed periodically (generally every 3 years) and registrants must keep registration certificates available at the registered location.