Controlled Substances Part 3: Prescribing and Dispensing Flashcards

1
Q

Which controlled substance schedules (if any) can each type of mid-level practitioner prescribe?

A

Nurse Practitioner: II-V as allowed in their written collaborative practice agreements and written protocols

Physician Assistant: II-V as allowed in the written agreement between the physician and PA

Optometrist: II-V

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2
Q

List the schedules of drugs collected in the state’s prescription drug monitoring program (PDMP).

A

All schedule II-IV drugs and drugs of concern.

Drugs of concern include:
1) Butalbital/acetaminophen/caffeine
2) Ephedrine or pseudoephedrine (if exempt from being reported to NPLEx)
3) Promethazine with codeine
4) Gabapentin

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3
Q

In what timeframe must a pharmacy submit the records of dispensed controlled substances to the state’s PDMP?

A

Outpatient pharmacies must report their prescription drug data to K-TRACS within 24 hours of the drugs being dispensed.

Pharmacies can submit “zero-claim” reports for periods during which they have not dispensed any controlled substance prescriptions. Zero-claim reports must be made every 7 days.

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4
Q

Which healthcare professionals are authorized to access the prescription drug monitoring program (PDMP)?

A

Prescribers and dispensers

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5
Q

Can controlled and non-controlled drugs be written on the same prescription form?

A

Not addressed in Kansas law

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6
Q

Is there a limit to the number of medications that can be written on one prescription form?

A
  • Yes, if the provider is issuing three 30-day Schedule II prescriptions to cover a 90-day supply.
  • Each prescription must be individually written on a separate prescription.
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7
Q

Other than prescriptions for Medicaid patients, do any prescriptions require tamper-resistant security forms?

A

No, Medicaid prescriptions only

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8
Q

What security elements must be present on tamper-resistant security forms?

A

Kansas follows federal regulations

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9
Q

What changes can be made, at the pharmacist’s discretion, to schedule II prescriptions?

A

A pharmacist may add the date issued if not written. They may add or change the drug strength, quantity, and directions for use after consulting with the prescriber or the prescriber’s agent. The prescriber’s DEA number may also be added. A dosage form may be selected if one is not written. Such consultations and all information added/changed must be initialed and dated.

The pharmacist is never permitted to make changes to the patient’s name, controlled substance prescribed (except for generic substitution permitted by state law), the prescriber’s signature, or any written date.

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10
Q

What changes can be made, at the pharmacist’s discretion, to schedule III - V prescriptions?

A

Address without consultation.

After consultation with the prescriber, can change dosage form, strength, quantity, directions of use and issue date.

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11
Q

What is the time limit (i.e., days/months) that a schedule II prescription must be filled from the date of issue?

A

Schedule II prescriptions are valid for 6 months from the date of issue

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12
Q

Is there a maximum quantity or days’ supply that a patient can receive of a schedule II drug?

A

No

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13
Q

Are partial fills for schedule II prescriptions permitted at the request of the patient or prescriber (if yes, list the requirements)?

A

Yes, a schedule II controlled substance may be partially filled at the request of the patient or the prescriber who wrote the prescription.

It must be filled within 30 days of the date the prescription was written.

The total quantity dispensed in all partial fillings cannot exceed the total quantity prescribed.

If the patient is in a Long Term Care Facility or has a terminal illness, the prescription can be partially filled for 60 days from the day the prescription was issued.

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14
Q

Are there any additional requirements for an emergency oral schedule II prescription compared to federal law?

A

No, Kansas follows the federal law.

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15
Q

Is there a maximum quantity or days’ supply that a patient can receive of schedule III - V drugs?

A

The only quantity limit is on controlled substances used for weight loss. The Board of Healing Arts limits each prescription to a 30-day supply.

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16
Q

How long are refills valid for schedule III, IV and V prescriptions?

A

6 months from the issue date

17
Q

What is the maximum number of refills allowed for schedule III, IV and V substances?

A

5 refills

18
Q

Can a pharmacist provide an emergency filling of schedule III - V drugs without the prescriber’s authorization?

A

Yes, except for any narcotic drug listed on any schedule of the uniform controlled substances act.

19
Q

What is the maximum days’ supply that can be dispensed for an emergency refill of schedule III – V drugs without prescriber authorization?

A

No more than a 7-day supply or one package of the drug

20
Q

What controlled drug schedules require identification for dispensing (e.g., schedule II only)?

A

Select schedule V medications (pseudoephedrine, brivaracetam, ezogabine, lacosamide and pregabalin) require patient identification prior to dispensing.

21
Q

Are pharmacists permitted to sell select schedule V cough syrups without a prescription?

A

Yes

22
Q

Is naloxone distribution by a pharmacist permissible in all situations, or is it pursuant to a standing order, a protocol or authorization from a prescriber?

A

It is permissible under a statewide protocol.

23
Q

What requirements must the pharmacist meet in order to furnish naloxone under the protocol (e.g., training program)?

A

To become a naloxone dispenser in the state of Kansas, a pharmacist must:

1) Read KAR 68-7-23, the statute that established the naloxone protocol.

2) Download, review and sign the official pre-signed statewide protocol.

3) Submit the protocol to the Board of Pharmacy within 5 days of signing.

You may also use a blank version of the protocol and work with another authorizing physician. In this case, the last page must be signed by both an authorizing physician and pharmacist.

24
Q

Other than exceeding the quantity limit, are there any conditions in which a pseudoephedrine sale can be rejected?

A

No