What part of the prescription includes the name and the quantity of the drug?

Definition/Introduction

Practicing clinicians, e.g., MDs, DOs, are often visited by patients because the patient is looking for medications to help remedy their chief complaint. There are five different levels of scheduling for medications (I-V), with schedule I having the tightest controls, and V being the least restrictive. There needs to be an understanding by the physician of the mechanism and properties of the medication before prescribing, and the pharmacist must be aware of potential interactions the patient may have with their other medications. 

Controlled substances are drugs considered to have the highest misuse and use disorder potential, and thus have the strictest regulation and prescription requirements on a federal and state level. To prescribe medication, a clinician must have a DEA (Drug Enforcement Administration) license; to fill a prescription, a pharmacist must also have a controlled substance license. schedule I medications (e.g., heroin), are unable to be prescribed or filled by a pharmacist because they have no indicated medical use in the USA. Schedule II drugs are the highest level of misuse potential medications that may be prescribed by a clinician; these drugs traditionally were only allowed to be filled by paper prescription; however, they are now prescribable via electronic prescribing of controlled substances (EPCS). Schedule III-V medications may be prescribed by a clinician via traditional paper prescription, by a verbal order over the phone, or using the EPCS system.[1][2]

The EPCS was implemented in 2010 by the DEA, which stated that clinicians might submit controlled substance prescriptions electronically; it also stated that pharmacies could dispense these electronic prescriptions. Using the EPCS from a clinician and pharmacy standpoint is voluntary, and each party may choose to use the system or not (however, some states such as New York are making the use of electronic prescribing mandatory with certain exceptions). Practitioners may still write and sign prescriptions for schedule II-V medications if they choose; verbal orders are only permitted for schedule III-V medications. The implementation of electronic prescribing has significantly reduced the number of medication errors from a prescription standpoint (legibility, dosage, frequency, etc.).[3][2]

For a pharmacist to dispense a controlled substance, the prescription must include specific information to be considered valid:

• Date of issue

• Patient’s name and address

• Patient's date of birth

• Clinician name, address, DEA number

• Drug name

• Drug strength

• Dosage form

• Quantity prescribed

• Directions for use

• Number of refills

• Signature of prescriber

There are legal limits on the number of refills and the number dispended that a prescription may have. For a schedule III-V drug, the maximum refills are 5, and the limit on quantity is 90 per allocation. Schedule II drugs have zero refills, and the maximum quantity dispensed is 30 days.[4]

Issues of Concern

Controlled substances are prescribable by a variety of clinicians: physicians, dentists, mid-level providers, podiatrists, etc. The prescribing practitioner must possess authorization from the DEA and have practicing rights within the given location of the prescription origin.

If there is any confusion for the pharmacist as to the reason for a prescription, or there are any other questions for the provider, then the pharmacist should contact the provider directly. A 2017 study showed that of prescriptions requiring clarification, 74% were new prescriptions, and only 36% of those needing clarification were electronically prescribed.  The most frequent reasons for the pharmacist to contact the prescriber were for prior authorization approvals and missing prescription information. The study found that the most efficient means to correct these miscommunications was telephone contact.[5]

Pharmacists play a crucial role in helping to limit the fraud that may occur, examples of potentially fraudulent activity are[4][2]:

• Stealing a clinician’s prescription pad

• Calling in medications pretending to be a clinician

• Altering a pre-existing prescription

It is important to remember that individual states may pass laws that alter how they govern the requirements of a prescription for different medications. An example of this is for marijuana, which at a federal level is considered a Schedule I drug, whereas some states permit its medical use and distribution. Pharmacists and practitioners should be familiar with the legislation within their practicing jurisdiction to provide the most appropriate patient care.[1]

However, in many instances, state law is more stringent than federal law. An example is drug monitoring systems for opioid prescriptions. Prescription drug monitoring programs are conducted on a state-by-state basis and are an electronic database of information on prescriptions filled within that state. The purpose of these monitoring programs is to limit drug abuse and addiction. Not all states at the time of writing this article have a fully operating monitoring program.[6]

Clinical Significance

Partial filling of a prescription for a schedule II medication is allowed if, and only if, the pharmacist is unable to provide the patient with the full quantity prescribed; the pharmacist must make a note on the written prescription or the electronic record of how many tablets or capsules were dispensed. According to the Controlled Substance Act, the completion of a partial dispensing of schedule II medications must take place within 72 hours of the initial allocation, after which the prescription is no longer valid for the remaining undispensed quantity. If this task cannot be completed, the pharmacist should contact the practitioner about obtaining a new prescription.[4]

Partial filling for a schedule II may also occur for patients in long-term care facilities or a patient with a terminal illness, so that the partial filling may be an individual dose; the pharmacist must document that the patient is terminally ill or in a long-term care placement before partially filling the medication. The remaining portion of the medication should be filled within 60 days from the prescription date unless the prescription is terminated because the medication is no longer necessary.[1]

Partial filling of schedule III-V medications can be completed within six months of the original prescription.[1]

A 2017 study found that there was a significant reduction in prescription errors for patients discharged from emergency departments when medications were prescribed electronically versus handwritten. The specific findings were that electronic prescriptions demonstrated decreased incidence of missed dosages, inaccurate frequency of medication, incorrect dosage strength, and the overall ability to read to the document (e.g., some clinician handwriting was illegible).[7]

Nursing, Allied Health, and Interprofessional Team Interventions

The healthcare team, e.g., physicians, nurses, pharmacists, etc., need to work together to address safe and effective pharmacotherapy in their patients especially with controlled substances.  The healthcare team should schedule their patients for routine follow-up visits that include a history and physical exam to monitor for adverse drug effects and drug misuse. Monitoring for signs of drug misuse is a very important responsibility for the healthcare team because of the epidemic rates of drug misuse worldwide, e.g., the USA, which can lead to death because of respiratory depression. Methods for monitoring drug abuse as well as drug diversion include the following examples: assessment surveys, state prescription drug monitoring programs, urine screening, adherence check-lists, motivational counseling, and dosage form counting, e.g., tablet counting. [Level 5]

Review Questions

References

Preuss CV, Kalava A, King KC. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Sep 21, 2022. Prescription of Controlled Substances: Benefits and Risks. [PubMed: 30726003]

Kaldy J. Controlled Substances Add New Layer to E-Prescribing. Consult Pharm. 2016 Apr;31(4):200-6. [PubMed: 27056356]

Volpe CR, Melo EM, Aguiar LB, Pinho DL, Stival MM. Risk factors for medication errors in the electronic and manual prescription. Rev Lat Am Enfermagem. 2016 Aug 08;24:e2742. [PMC free article: PMC4990040] [PubMed: 27508913]

Gabay M. Federal controlled substances act: dispensing requirements, electronic prescriptions, and fraudulent prescriptions. Hosp Pharm. 2014 Mar;49(3):244-6. [PMC free article: PMC3971109] [PubMed: 24715743]

Smith M, Sprecher B. Pharmacy communications with physician offices to clarify prescriptions. J Am Pharm Assoc (2003). 2017 Mar-Apr;57(2):178-182. [PubMed: 28161301]

Deyo RA, Hallvik SE, Hildebran C, Marino M, Springer R, Irvine JM, O'Kane N, Van Otterloo J, Wright DA, Leichtling G, Millet LM, Carson J, Wakeland W, McCarty D. Association of Prescription Drug Monitoring Program Use With Opioid Prescribing and Health Outcomes: A Comparison of Program Users and Nonusers. J Pain. 2018 Feb;19(2):166-177. [PMC free article: PMC5803414] [PubMed: 29054493]

Hitti E, Tamim H, Bakhti R, Zebian D, Mufarrij A. Impact of Internally Developed Electronic Prescription on Prescribing Errors at Discharge from the Emergency Department. West J Emerg Med. 2017 Aug;18(5):943-950. [PMC free article: PMC5576632] [PubMed: 28874948]

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