What is the prescription monitoring program (PMP) used for?
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1 pt
DEA Inventory vs NMBoP
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1 pt
What is the Mission of PMP?
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1 pt
What should be included in a PMP request?
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1 pt
SB 221
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1 pt
what should dispenser do if becomes aware of an data entry error?
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1 pt
When should a pharmacist request and view the PMP?
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30 seconds
1 pt
True
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30 seconds
1 pt
What are the signs of opioid abuse or misuse?
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30 seconds
1 pt
Food additives
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1 pt
Blood and blood products
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1 pt
Medical devices
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1 pt
Cosmetics
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1 pt
Compounded prescription drugs
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1 pt
Consumable alcohol products
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1 pt
Tobacco products
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1 pt
Food Pesticides
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1 pt
What is the title number of the Code of Federal Regulations specific to the regulation of foods and drugs?
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1 pt
According to the controlled substances act, which of the following do not have to register with the DEA to handle controlled substances
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1 pt
NMSA Chapter 24
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1 pt
NMSA Chapter 30
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1 pt
NMSA Chapter 26
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1 pt
26-1-16
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1 pt
26-1-16-1
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1 pt
NMSA Chapter 61
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Chapter 61 . Artical 11 NMSA 1978
61-11-1
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1 pt
61-11-11
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1 pt
The NM Drug Product Act allows pharmacists to substitute the prescribed drug with another (generic substitutions) under which condition?
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1 pt
Which legislation delegates regulatory authority to the NM Board of pharmacy, established pharmacist licensing requirements, and sets regulations delineating who can sell prescription drug?
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1 pt
Name the 1962 Amendment to the Food Drug & Cosmetic Act, which was enacted in response to the drug thalidomide. This amendment requires that drug manufacturers to provide proof that drugs are both safe and effective.
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1 pt
Kefauver-Harris Amendment was in response to
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Kefauver-Harris Amendment requires
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1 pt
What are the two main accomplishments of the Durham Humphrey Amendment
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1 pt
becomes aware of a person currently exhibiting potential abuse or misuse of opioids
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1 pt
an opioid prescription issued by a prescriber with whom the pharmacist is unfamiliar
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1 pt
opioid prescription for an unfamiliar patient who resides outside the usual pharmacy geographic patient population area
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1 pt
initial prescription for any long-acting opioid formulations, including oral and transdermal dosage forms (e.g fentanyl or methadone)
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1 pt
aware of a patient receiving an opioid concurrently with a benzodiazepine or carisoprodol
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1 pt
T/F pharmacists must document PMP review
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1 pt
T/F PMP reports shall be reviewed a minimum of once every three months during the continuous use of opioids for each established patient
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1 pt
T/F if the PMP system is not in operation, the pharmacist may not dispense controlled substances
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1 pt
Tobacco Cessation
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1 pt
TB testing
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1 pt
Naloxone for opioid overdose
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1 pt
Hormonal Contraception
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1 pt
Vaccines
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1 pt
Emergency Contraception
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1 pt
CI
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1 pt
CII
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1 pt
CIII
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CIV
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CV
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Dispensing CIII-CV
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1 pt
Dispensing CII
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1 pt
Pseudoephedrine
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1 pt
16.29.26
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1 pt
Defined for each prescriptive authority authorized by the NMBOP
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1 pt
Protocol
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1 pt
Records
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1 pt
education and training
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1 pt
authorized drugs
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1 pt
notification
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1 pt
Autonomy
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1 pt
Beneficence
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1 pt
Nonmaleficence
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1 pt
Confidentiality
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1 pt
HIPAA violation
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1 pt
HIPAA
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1 pt
Veracity (AKA Truthfulness)
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1 pt
Justice
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1 pt
Fidelity or Promise Keeping
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1 pt
A Process For Ethical Decision making
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1 pt
Barriers to Ethical Practice
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agency with in DHHS
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1 pt
Responsible for enforcing federal laws like the Food Drug & Cosmetic Act
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1 pt
Develops regulations based which become law (Title 21 Code of Federal Register)
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1 pt
Issues guidance ( not law) as FDA current thinking on a regulatory issue.
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1 pt
In the case of food supplements , the F.D.A. does almost nothing to ensure that dietary supplements work as advertised. It is only when supplements are proved to be unsafe or to contain regulated substances can the agency take action.
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1 pt
The government agency responsible for regulating food, dietary supplements, drugs, cosmetics, medical devices, biologics and blood products in the United States.
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1 pt
Approval of drugs on the basis of purity, safety and effectiveness.
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Regulation of all labeling for prescription and nonprescription drugs.
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Regulation of advertising for prescription drugs (The Federal Trade Commission [FTC] regulates nonprescription advertising).
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1 pt
Regulation of manufacturing processes of drugs and institution of recalls.
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1 pt
Regulation of bioequivalence for generics and biosimilars.
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1 pt
Monitoring of drugs post-approval to detect any problems with the use of drugs, such as unanticipated adverse reactions (a.k.a.- postmarketing surveillance)
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1 pt
Monitoring of the safety of the nation's blood supply.
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1 pt
T/F the FDA maintains direct control over how a drug is used or prescribed after the drug is approved
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1 pt
a US federal law enforcement agency under the US Department of Justice.
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1 pt
Responsible for the enforcement of the provisions of the Controlled Substances Act as they pertain to the manufacture, distribution, and dispensing of legally produced controlled substances.
90. Fill in the Blank
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1 pt
A _______________ is a written law passed by a legislature on the state or federal level.
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1 pt
set forth general propositions of law that courts apply to specific situations.
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1 pt
Changes require amendment by the legislative body.
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1 pt
Federal vs State Law
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1 pt
The ______ grants the state government the authority to regulate pharmacy practice not granted to the federal government by the constitution
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1 pt
Statutes are passed by the state legislature and enforced by ______.
96. Fill in the Blank
30 seconds
1 pt
Laws relating to the health, safety and welfare of its people belong (mostly) to the ______.
97. Fill in the Blank
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1 pt
the _______ gives federal authority to regulate drug distribution.
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1 pt
designed to increase flexibility and efficiency in the operation of laws.
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indirectly enforceable laws
100. Fill in the Blank
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1 pt
Most _______ are developed and enacted through a rule-making process, which includes public input
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1 pt
NMBOP
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1 pt
NM houses all state regulations in the New Mexico Administrative Code. The Chapter specific to the practice of pharmacy in New Mexico is _____
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1 pt
Pure Food and Drug Act of 1906-
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1 pt
Pure Food and Drug Act of 1912-
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1 pt
Food Drug and Cosmetic Act- 1938
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1 pt
Established prescription-only classification
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1 pt
T/F drugs marketed before 1938 were excluded from the law
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1 pt
Durham-Humphrey Amendment of 1951
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1 pt
Kefauver-Harris Amendment of 1962
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1 pt
NM Drug, Device and Cosmetic Act
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1 pt
NMSA Chapter 26
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1 pt
Misbranding
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1 pt
Adulteration
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1 pt
NM Drug Product Selection Act
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1 pt
NM Controlled Substances Act
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1 pt
How many BOP districts are there
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1 pt
NM Pharmacy Act
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1 pt
NM Impaired Pharmacists Act
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1 pt
A patient bring is a new prescription for fentanyl patches. Should the pharmacist check a PMP
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1 pt
A patient brings in two prescriptions one for oxycodone and one for alprazolam. Should the pharmacist check the PMP