Child Resistant PPPA 1970
OSHA 1970
OBRA 1990
Record Keeping
Miscellaneous
100


What does PPPA stand for?



Packaging and Poison Prevention Act


100


What does OSHA stand for?



Occupational Safety and Health Administration

100
  1. What is the Omnibus Budget Reconciliation Act of 1990?

A federal law outlining responsibilities of pharmacists and the pharmacy for counseling of medicaid patients (now it applies to everyone). 

  • Only pharmacists can counsel patients and offer counsel on medication use. 

  • Pharmacists must complete medication records and they must DUR’s (Drug Utilization Reviews) before dispensing meds. 

100

Where do you place the Rx label on the original prescription, and what do you do with it?

  • On the back of the original prescription, and must be filed

100

What are some forms of abuse in a pharmacy setting?

  • Using illegal substances

  • Billing for unnecessary medical services

200


What does the PPPA do?



requires specific child resistant packaging for all prescriptions unless excluded by the PPPA, inpatient medications or otherwise requested by prescriber or patient. packaging is required to function in that 80% of children under 5 years old cannot open container and 90% of adults CAN open within 5 minutes

200


What does OSHA do?



Helps ensure safe and healthy working conditions by setting and enforcing standards


200
  1. What are indicators of prescription forgery?

  • Very neat handwriting 

  • Appears photocopied 

  • Multiple ink colors 

  • No medical/pharmacy acceptance abbreviations 

  • Unusually large amount of medication 

  • Visible alteration 

200

Patient Profiles should contain what information?

  • Demographics 

  • SSN

  • RX History

  • Medication Allergies & Intolerances

  • Chronic Conditions or Diseases

  • Insurance Information

  • Patient Notes or Preferences

200

Why was the Opioid Rapid Response program created?

  • Reduce the risk of overdose deaths

300


Why do medications have child prevention packaging on them?




To make it more challenging for children under five to open,  slowing them down and reducing fatalities


300


How do you dispose of sharps?



Dispose of them immediately in a rigid, designated, impenetrable container - usually red with a biohazard symbol


300
  1. What are some examples of healthcare fraud that pharmacies must watch out for?

  • Submitting false health insurance claims

  • Using someone else’s insurance card

  • Forging/altering prescriptions

  • Selling personal prescriptions 

300

Patient records are referred to what under OBRA

“Patient Profiles”

300

Which act regulates the manufacture, importation, possession, use, and distribution of medications and substances that have the potential for abuse and/or psychological dependence?

Controlled Substances Act

400


If patients wish for a non-child-proof cap on a prescription, what must they do?



Must sign a waiver, where the pharmacy will keep this on file. Then, affix a warning label on the prescription bottle


400


How do you dispose of hazardous materials?




Usually placed in a waste receptacle, which is typically yellow


400
  1. In the instance that you detect fraudulent behavior, what are the measures you should take?

  • Refuse the prescriptions, alert law enforcement, and use the government reporting system to document this encounter.

400

In most cases, original prescriptions, either electronic or physical, must be kept for a minimum of:

 2 years

400

When was HIPAA established?

1996

500


What form of drug is not permitted to have a child-proof cap?



Nitroglycerin sublingual tablets. They must be dispensed in their original unopened containers


500


How do you dispose of biological materials?



Biological materials go in a red bag


500
  1. What is considered “waste” or “wasteful behavior” in the pharmaceutical profession?

  •  Inefficiencies within the system causing dispensed products to become unused or adding unnecessary cost to dispensing medications


    1. Patient non-adherence to the prescription

    2. Dispensing a brand name (if alternatives could supplement it) 

    3. Changes in medication therapy regimens or transition of care that could cause the already-dispensed medication to no longer be used by the new provider or system. 

500

What is wrong with submitting the brand name medication to insurance while dispensing the generic version?

It's directly related to waste and abuse as billing for a brand name and dispensing the generic version would constitute unnecessary billing or charging excessively for services. 
500

What is the best description for a black box warning?

The FDA’s strongest warning about serious or life-threatening risks/ high risk potential

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