Instrument to Evaluate the Level of Knowledge About Prescription In

Total Page:16

File Type:pdf, Size:1020Kb

Instrument to Evaluate the Level of Knowledge About Prescription In Rev Saúde Pública 2010;44(6) Samanta Etges FröhlichI Instrument to evaluate the Tatiane da Silva Dal PizzolII Sotero Serrate MengueII level of knowledge about prescription in primary care ABSTRACT OBJECTIVE: To develop and test an instrument to evaluate patients’ level of knowledge about drug prescription. METHODS: This study was conducted with users registered with the Family Health Strategy clinics of the city of Santa Cruz do Sul, Southern Brazil, selected by consecutive sampling. Name of the medication, therapeutic indication, drug dosage, times of administration, forms of use, duration of treatment, attitude when doses are missed, possible adverse effects and interactions were included in this study. Each item of the scale was weighted, according to the importance for safe prescribed drug use. The questionnaire was tested by applying an interview to users in 2006 and by analyzing 320 prescriptions. Descriptive statistics, prevalence ratios and chi-square test were calculated for categorical variables and the Tukey test was calculated to compare means. RESULTS: The level of knowledge about drug therapy was considered good in 11.3% of participants, fair in 42.5%, and insuffi cient in 46.3%. The highest levels of knowledge were observed in times of administration, therapeutic indication and duration of treatment. The lowest levels occurred in drug dosage, adverse effects and attitude when one or more drug doses are missed. CONCLUSIONS: The proposed instrument enabled the analysis of the magnitude of the gap existing between what the patients must know and what they actually know about their medications. Thus, key aspects of prevention, education and follow-up can be detected to avoid problems associated with unsafe drug use. DESCRIPTORS: Patients. Health Knowledge, Attitudes, Practice. Drug Prescriptions. Primary Health Care. Questionnaires. I Programa de Pós-Graduação em Epidemiologia. Universidade Federal do Rio Grande do Sul (UFRGS). Porto Alegre, RS, INTRODUCTION Brasil In Brazil, it is diffi cult to obtain drugs, specifi c therapeutic drug classes are II Departamento de Medicina Social. UFRGS. 14 Porto Alegre, RS, Brasil under-used and new pharmaceutical products are misused. In addition, there are distortions of aspects comprising all drug manufacturing and supply Correspondence: processes and inadequate drug use.13 Fulfi llment of drug prescriptions is an Samanta Etges Fröhlich integral part of high-quality clinical care and an object of improvement and R. Visconde do Herval, 556 Apt. 304 4 Menino Deus evaluation. This fulfi llment is related with the patient’s level of information 90130-150 Porto Alegre, RS, Brasil about their therapy.5,15 Their knowledge about the prescription can refl ect the E-mail: [email protected] communication between doctor and patient and the cultural and language Received: 5/29/2009 differences existing between them. Approved: 8/19/2010 The information provided to patients must be written preferably, because they Article available from: www.scielo.br/rsp can forget it or not understand it correctly, which would hinder the fulfi llment 2 Evaluation of knowledge about prescription Fröhlich SE et al of the therapy.16 Studies show that this information This study included individuals with the following includes: generic or trade name of the medication, characteristics: to be aged more than 18 years, to therapeutic indication, drug dosage, times of admin- accept participating in the research, to be able to istration, forms of use, duration of treatment, attitude communicate adequately, to have used one of the ESF when dosages are missed, possible interactions with medical services during the data collection period, and foods or other drugs, relevant adverse effects, risks of to have received a medical prescription that needs to dependence and adequate storage.1,7,20,21,a be fulfi lled. Users who met the inclusion criteria and were available after consultation were interviewed, Misunderstanding the prescription may be the result using consecutive sampling. of lack of information,17 failure to interpret and read it, or previous experiences the patient had with the Responses to questions were transcribed and compared drug.11 Questions about the prescription may cause an to the medical prescription. Items not expressed individual to feel unmotivated, change it according in the prescription (therapeutic indication, attitude to their criteria or stop following it. In addition to the when dosages are missed, adverse effects and inter- correct diagnosis and adequate prescription, the patient actions) were based on a publication of the United must have the necessary information to use the drugs, States Pharmacopeia Drug Information (USP DI).19 according to the professional’s intention, that is opera- Participants’ responses were classified into the 6 tionalized by medical prescription. following categories, according to the level of agree- 19 It is recommended that the patient should receive ment with the prescription and in this publication: information about drug identifi cation (generic or brand 1) does not know, 2) thinks he/she knows (wrong name), therapeutic indication, drug administration response), and 3) knows. (dosage, times, forms of use), duration of treatment, The name of the medication was considered correct relevant adverse effects and precautions, among other when pronounced correctly or similarly to the generic things.1,21,a or brand name of any product commercialized in Brazil Aiming to identify the gap that may refl ect the differ- with the active substance in question. The therapeutic ence between safe drug use and non-adherence to treat- indication was regarded as adequate when there was ment, the objective of the present study was to develop agreement with the therapeutic drug class (differences and test an instrument to evaluate patients’ level of between technical and popular terminology were not knowledge about prescription in primary care. considered). The dosage was considered correct when there was agreement between the patient response and the amount to be administered at each time. In addi- METHODS tion to the International System Units, responses given A literature review was conducted to develop the instru- in dosage units, such as “one pill”, were classifi ed as ment used to evaluate patients’ level of knowledge correct. Times, forms of use and duration of treatment about drug prescription. (agreement between patient response and the acute or chronic nature of the prescribed treatment) were A questionnaire was designed, aiming at an empirical analyzed in the prescription and, when there was no model founded on a theoretical model, as proposed by information in such sources, in the pharmacological Presser et al12 (2004) (Attachment). This instrument literature.17 For the items not described in the prescrip- was applied by previously qualifi ed Pharmacy students tion, responses were considered correct when there using face-to-face interviews. was at least one adverse drug effect and any proper attitude that was reported when dosages were missed Participants in this study were users registered with or with regard to the interaction between food and/or Family Health Strategy (ESF) clinics of the city of medications. Santa Cruz do Sul, Southern Brazil. In September 2006, the city was served by eight ESF clinics, in different The interpretation of the existence of an agreement districts, which cared for 8,149 families and 28,863 between patient responses and the information present users (24.1% of the total population).b Health educa- in the prescription and pharmaceutical literature was tion was provided in group services, which included conducted independently by two reviewers. In cases of hypertensive patients, diabetics, pregnant women, and disagreement, a third reviewer was consulted. mothers with low-weight children, in addition to health programs for women, children, adolescents, alcoholics, The scale was constructed so that each item was elderly individuals and family planning.b weighted, according to the importance for safe drug a German Foundation for International Development. Report of the 1o International Seminar on Improving Acess to Drug Information in Developing Countries; Berlin, Germany; 1995. b Prefeitura Municipal de Santa Cruz do Sul. Secretaria Municipal da Saúde. Plano Municipal de Saúde de 2006. Santa Cruz do Sul; 2006[cited 2006 Sep 15]. Available from: http://www.pmscs.rs.gov.br/index.php?acao=areas&areas_id=17 Rev Saúde Pública 2010;44(6) 3 use. Indispensable items for the patient to identify and knowledge” and “level of education” variables were administrate the medication received higher scores. dichotomized into: low (less than eight points) and high A total of two points were attributed if the user really (from eight to 13 points) and low (incomplete primary knew the name of the medication, the dosage, the form education) and high (complete primary education or of administration and its frequency. Information not higher), respectively. directly related to drug administration, which could, however, be important for adherence to treatment, Tukey test was used to compare the mean levels of received lower scores. If the user knew the therapeutic knowledge for the main prescribed drug classes. indication, the duration of treatment, any adverse effect, Descriptive and explanatory statistical analyses were any interaction with foods or other medications, and performed in the SPSS 13.0. Frequencies, means, what to do if one or more dosages were missed, one standard-deviations, prevalences, prevalence ratios and point was attributed. The level of knowledge about chi-square were estimated for categorical variables and drug prescription was obtained by adding up correct the Tukey test was used to compare different means. responses and considering the weights {mathematical formula: score = (q1 + q3 + q4 + q6 (x2)) + (q2 + q5 The present study was approved by the Santa Cruz + q7 + q8 + q9)}. do Sul Department of Health (official letter 530/ SMS/2005/PF) and the Research Ethics Committee of Cut-off points were attributed based on similar the Universidade Federal do Rio Grande do Sul (process studies,7,16,20 and patients were classifi ed into one of 2005450).
Recommended publications
  • Medical Prescription Market Definitions
    Horvath Health Policy Innovations in Healthcare Financing Policy PO Box 196, College Park, MD 20741 202/465-5836 [email protected] Medical Prescription (Rx) Market Definitions Drug Product Terminology Small Molecule Drugs: Drugs with an active chemical ingredient that is not live, but chemically synthesized and typically are taken orally or topically, such as capsules, tablets, powders, ointments, and sprays. Brands: Also referred to “small molecule drugs,” brand drugs require original research and development for FDA licensure (also called “FDA approval”). They are approved (or licensed) under a New Drug Application (NDA). They are patent protected for 20 years total (which usually includes years clinical research before the drug is approved, or licensed). They are still referred to as brands even after the patent has expired (which distinguishes these drugs from generics). A brand can be ‘first in class” if it is a new chemical entity or new mechanism of action. It is a “me too drug” if it is not first in class. The definition of “me too” varies – different chemical composition, different mechanism of action. The drug is quite similar but different enough to get a patent. Generic: Small molecule products that are demonstrated to be clinically equivalent to a branded product (e.g., same active ingredient and route of administration, same mechanism of action). Generics do not require original research for FDA approval. Generics come to market only after the patent has expired on the brand product. Licensed under an Abbreviated New Drug Application (ANDA) by the FDA. Large Molecule Drugs: Commonly referred to as “biologics” and “biosimilars.” They contain live active ingredients and are generally infused or injected, and otherwise not taken orally or topically.
    [Show full text]
  • The Internet and Adolescent Non-Medical
    The Internet and Adolescent Non‐Medical Use of Prescription Drugs Background Sales of psychoactive prescription drugs over the Internet are becoming a major enterprise, presenting new challenges to drug abuse prevention and treatment. Adolescent non- medical use of highly addictive prescription opioid drugs, such as Vicodin and Oxycontin; sedatives, such as Ambien; and tranquilizers, such as Valium and Xanax, is increasing (Johnston et al 2005, SAMHSA 2005). These increases are occurring in the face of the otherwise encouraging news that among youth ages 12 to 17, past month illicit drug use overall has declined 19% since 2001 (SAMHSA 2005). Although the reasons for increasing adolescent non-medical use of addictive prescription drugs are not known, we do know that they are widely advertised and sold over the internet without prescription. Ready availability through “non-prescription websites (NPWs)” may be one important contributing factor to increasing adolescent use of these drugs (Kissinger 2004). The Director of the National Institute on Drug Abuse (NIDA), the Director of the Office of National Drug Control Policy (ONDCP) and the Administrator of the Drug Enforcement Administration (DEA) all believe that “rogue online pharmacies” have become a significant source of drugs for adolescents (Volkow 2004, Office of National Drug Control Policy 2004). The global reach of the internet now makes it as easy for an adolescent to buy drugs as it is to buy a book or CD with a credit card, PayPal, or even cash. Some sites provide drugs initially for free without immediate payment. Unlike many scams on the internet, there is ample evidence that these drugs of abuse are real, potent, and actually delivered to buyers.
    [Show full text]
  • FAQ Prescription Questions By: Kandi Rasmussen, LVT
    10261 County Road P38A ~ OMAHA, NE 68142 PHONE: 402-533-1151 ~ FAX: 402-533-1159 Email: [email protected] Michael J. Black D.V.M. Michael P. Thomassen D.V.M. Kimberly N. Conover D.V.M. ______________ Exp: ______ Th FAQ Prescription Questions By: Kandi Rasmussen, LVT Every day we prescribe medications to treat our patients. Every day we answer questions and requests concerning medications from our clients. We love your questions but we have come to realize that there are a few common questions that are asked routinely. These routine questions sparked this article. Are all medications we dispense to clients prescription items? No they are not. A prescription medication or drug is defined as a pharmaceutical drug that legally requires a medical prescription to be dispensed. In contrast, over-the-counter drugs (OTC) can be obtained without a prescription. Just like human medicine there are two kinds, prescription and OTC, we use and recommend both. Many medications are prescription only because prescription drugs are only effective for specific problems, and may actually be harmful to your horse if used without that critical veterinary examination and diagnosis. Having these drugs available as prescription-only medications ensures that they are used appropriately. Can I get a prescription for a medication? This question has two answers. Yes, every time we prescribe a prescription drug or medication your horse then has a prescription for that specific medication with specific instructions to be give for a specific amount of time to treat a specific problem. No, we cannot prescribe a medication for a horse or a problem that we have not seen because “Veterinary prescription drugs are those drugs restricted by federal law to use by or on the order of a licensed veterinarian.” In order for a veterinarian to order a medication there must be a valid Veterinarian/Client/Patient Relationship (VCPR).
    [Show full text]
  • WHO EDM QSM 00.1 Eng.Pdf
    ©World Health Organization (2000) This document is not a formal publication of the World Health Organization (WHO). All rights are reserved by WHO. The document may, however, by freely reviewed, abstracted, reproduced or translated, in part or in whole, but not for sale or use in conjunction with commercial purposes. The views expressed in this document by named authors are solely the responsibility of those authors. Guidelines for the Regu latory Assessment of Medicinal Products for use in Self-Medication World Health Organization Geneva 2000 1. Introduction Self-care can be defined as the primary public health resource in the health care system. It consists of the health activities and health-related decision-making of individuals, families, friends, colleagues at work, and so on. It includes self-medication, non-drug self-treatment, social support in illness, and first aid in everyday life. The reclassification of medicinal products from sale on prescription only to non­ prescription (over-the-counter, or OTG) sale is of great current interest in many countries. Drug regulatory and health authorities have to consider the types of medicinal products for which reclassification is appropriate, safe and rational in the interest of public health. It has become widely accepted that self-medication has an important place in the health care system. Recognition of the responsibility of individuals for their own health and awareness that professional care for minor ailments is often unnecessary have contributed to this view. Improvements in people's general knowledge, level of education and socioeconomic status in many countries form a reasonable basis for successful self-medication.
    [Show full text]
  • Electronic Health Records: a Global Perspective
    Electronic Health Records: A Global Perspective Second Edition Part I A Work Product of the HIMSS Enterprise Systems Steering Committee and the Global Enterprise Task Force August, 2010 © 2010 Healthcare Information and Management Systems Society (HIMSS). Global Enterprise Task Force Chair, Steve Arnold, MD, MS, MBA, Co-Chair, Walter W. Wieners, CPE FHIMSS President & CEO Managing Principal Healthcare Consultants International Walter W. Wieners Consulting Lagrangeville, New York Sausalito, California Global Enterprise Task Force Members Contributors to the White Paper Dorothea LaChon Abraham, PhD Belinda Eliahu Assistant Professor Director of Marketing Mason School of Business dbMotion Ltd. College of William & Mary Israel Visiting Assistant Professor Keio University Guilherme S. Hummel Japan International Consultant and Researcher Brazil Marion J. Ball, EdD, FHIMSS, FCHIME Pramod Jacob Fellow Chief Consultant IBM Center for Healthcare Management DJ Health-Tech. Professor Emeritus Goa, India Johns Hopkins School of Nursing Baltimore, Maryland Selene Kepila Chairman and Executive Director Dr. Ngai Tseung Cheung CareData Solutions Corporation Chief Medical Informatics Officer Hong Kong Hospital Authority Georg Heidenreich Hong Kong Manager, Healthcare IT Siemens AG Healthcare Laurent Debenedetti Erlangen, Germany Direction generale Relations internationals Susan J. Hyatt, BSc (PT), MBA Sante Government President & CEO France HYATTDIO INC Oakville, Ontario, Canada Dr. Harald Deutsch Vice President Healthcare EMEA Computer Sciences Corporation Germany ©2010 Healthcare Information and Management Systems Society (HIMSS). 2 Gary M. Klein, MD, MPH, MBA Erik Pupo Former Consultant & Chief Medical Senior Enterprise Architect Information Officer Pearson Blueprint Technologies Department of Homeland Security Vienna, Virginia Washington, DC Current President Chong Yoke Sin The American Academy of Disaster Chief Executive Officer Medicine Singapore MOH Holdings Singapore Susheel Ladwa Practice Leader, Healthcare and Life Sanjay P.
    [Show full text]
  • Infosys Telemedicine
    INFOSYS TELEMEDICINE Infosys telemedicine solution is designed for doctors and nurses to manage patients, their requests, and provide consultation. The solution captures all the information related to a patient throughout his/her life cycle, including past medical history and treatments, biometric data, etc., thereby providing a 360 degree view of the patient to the medical representatives. The doctor gets consolidated information that helps them make accurate decisions that are communicated back to the patient with a quick turnaround time. Easy and secured path taken by health professionals Attending physicians Welcome, informaton, and to rt Medical po orientation re consultation a nd Patient Se Dedicated number Fax In case of medical prescription Nurse Physician C all w ith ph armaci st Pharmacy Go to the selected pharmacy Solution benefits • Visibility of patient record depending • Captures the biometric details, past upon the individual doctor's access medical history, and treatment • Remote health consultation information • Analysis of patient medical history and • Effective and convenient communication consultation information • Assists in assessing the medical situation between patient and medical staff of the patient • Easy access to medical services • E-prescription / e-diagnosis / radiology prescription, etc. Request outcome • Quick transmission of prescriptions, • Based on patient query and his/her reports, and other consultation-related Solution features medical context, the request outcome data Dashboards is decided • Automated
    [Show full text]
  • Texas Pill Mills the Prescription Opioid Epidemic
    Texas Pill Mills The Prescription Opioid Epidemic October 30, 2016 Lisa Sullivan, DPM DEA Dallas Division Lisa Sullivan Ms. Lisa Sullivan is an alumnus of New Mexico State University where she graduated with a Bachelor of Criminal Justice degree in 1989. She began her career with the DEA in 1990 as a Diversion Investigator in the San Antonio District Office. In 2000 she became the Diversion Group Supervisor in the San Antonio Office. The group was responsible for the dismantling and successful prosecution of one of the first internet pharmaceutical cases in the country. In 2005 Ms. Sullivan was transferred to the E-Commerce Section of the Office of Diversion Control DEA in Washington DC. There she worked on the CSOS program (the newly established controlled substance electronic ordering system), the SearchPoint prescription database, and the electronic prescriptions initiative (EPCS). She helped present and establish protocols for the Distributor Initiative which addresses the excessive or unusual sales of legitimate pharmaceuticals by distributors. In 2007 she was assigned to the office of Enforcement Pharmaceutical Section DEA HQ where she continued to establish targets for future deployments with regards to internet pharmacy investigations. In November 2007 Ms. Sullivan was transferred to the position of Diversion Program Manager for the Dallas Division where she establishes priorities and direction for the Diversion Groups in Dallas, Ft. Worth, and Tyler, Texas, as well as Oklahoma City, and Tulsa, Oklahoma. Ms. Sullivan has no relevant
    [Show full text]
  • Prescription
    Prescription A medical prescription (℞) is an order (often in written form) issued by a qualified health care professional (e.g. physician and dentist) to a pharmacist or other therapist for a treatment (medicine or device) to be provided to their patient. There are two broad legal classifications of medications: • The medications which can be obtained only by prescription which are referred as prescription drugs or legend drugs. • The medications which may be purchased without a prescription, which are termed non prescription drugs or over-the-counter (OTC). COMPONENTS OF PRESCRIPTIONS Generally, a prescription consists of the following parts (see the sample prescription in Figure 3.1). (1) Prescriber’s name, degree, address and telephone number. In the case of prescriptions coming from a hospital or a multicenter clinic, the hospital or clinic’s name, address and telephone numbers appear at the top. In such a case, the physician’s name and degree would appear near his/her signature. (2) Patient’s name, address, age, and the date of prescription. (3) The Superscription, which is represented by the Latin sign. (℞). This sign represents ‘‘take thou’’ or ‘‘you take’’ or ‘‘recipe.’’ Sometimes, this sign is also used to denote the pharmacy itself. (4) The Inscription is the general content of the prescription. It states the name and strength of the medication, either as its brand (proprietary) or generic (nonproprietary) name. In the case of compounded prescriptions, the inscription states the name and strength of active ingredients. (5) The Subscription represents the directions to the dispenser and indicates the type of dosage form or the number of dosage units.
    [Show full text]
  • FOR PREVENTION: PREVENTION: Non-Medical Prescription Drug Use Toolkit for Health Promotion Professionals
    FORFOR PREVENTION: PREVENTION: Non-Medical Prescription Drug Use Toolkit for Health Promotion Professionals © Stacy Andes Ed.D, 2010 FORFOR PREVENTION: PREVENTION: Non-Medical Prescription Drug Use Toolkit for Health Promotion Professionals Table of ConTenTs Executive Summary .................................................................................................................................................1 Introduction .............................................................................................................................................................3 Materials in Toolkit .................................................................................................................................................. 4 Data Sources & Tools ....................................................................................................................................5 Prevention Strategies .....................................................................................................................................7 Resources .............................................................................................................................................................28 Supplemental Handouts .............................................................................................................................. 33 PowerPoint Template Notes ....................................................................................................................... 45 AcknowledgemenTs
    [Show full text]
  • Telemedicine in Europe
    Telemedicine in Europe The European telemedicine industry is on the rise as a result of recent legalisation of activities like remote treatment and electronic prescriptions in most countries. Telehealth became a very popular and important topic in light of new challenges like the global COVID-19 pandemic, which rapidly accelerated the far-reaching developments that were already taking place in the telemedicine market. As a result, the number of suppliers in the European telemedicine industry is expected to increase in the nearest future since European countries are among the largest healthcare markets in the world. The following sections provide a brief overview of the national developments and legal frameworks regarding telemedicine in Germany, France, Belgium, Italy, Spain, the Netherlands and the UK. Select a section from the navigation on the left and then choose the country-specific information from the navigation at the bottom. Belgium France Germany Italy The Netherlands Spain UK 1. What is telemedicine? 1. What is telemedicine? There is no definition of telemedicine under Belgian law. The Belgian Physicians’ Association describes telemedicine as the use of telephone notice, electronic notice and prescription, telemonitoring (remotely, by video conference and by medical applications), teleconcertation between professionals and the storage of health data in the cloud. Belgium 1. What is telemedicine? 1. What is telemedicine? France is one of the exceptions in having a legal definition FCPH further defines five activities of telemedicine: of telemedicine, which is provided in Article L6316-1 of the – Teleconsultation: a healthcare professional’s remote medical French Code of Public Health (FCPH): consultation for a patient.
    [Show full text]
  • Feasibility Study on Moving Towards Electronic Prescription Over Manual Prescription Dharmendra Godhani1, Prerna Singh2, Deeksha Jangdekar3, Nikita Thadani4
    International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 03 Issue: 01 | Jan-2016 www.irjet.net p-ISSN: 2395-0072 Feasibility Study on Moving Towards Electronic Prescription over Manual Prescription Dharmendra Godhani1, Prerna Singh2, Deeksha Jangdekar3, Nikita Thadani4 1234 B.E Scholar, Computer Science and Engineering, Jhulelal Institute of Technology, Nagpur, India ---------------------------------------------------------------------***--------------------------------------------------------------------- Abstract - Think about the world without any manual towards making India digital and simplifying the work of work what if we reduce the work in which human has to doctors as well as chemist. put lots of efforts not in thinking but doing manual This paper is about Prescription Writing app, for doctors, work. What if we make our world A SMART WORLD, So which saves time, avoids paperwork trouble and is a here is one such approach that we are taking to make convenient tool to maintain patient’s record and reduce our city smart. This paper is a small contribution the overhead of understanding manual documented towards making India digital and simplifying the work prescription given by doctor’s . It allows the receptionist of doctors as well as patients. It allows the receptionist to enter patient’s general information which includes name, age, address, gender, contact no. of patient, etc and to enter patient's general information which includes add them in a queue of patients waiting for the treatment. name, age, address, gender, contact number of patient, Doctor will be able to keep a watch on patients that are in etc. Doctor will be able to keep a track on patients who queue as well as how many patients it has to attend.
    [Show full text]
  • Pharmacy Provider Manual
    Pharmacy Provider Manual All Rights Reserved This Pharmacy Providers Manual and other documents provided to Participating Pharmacies owned by MC-21, are confidential and remain the property of MC-21 LLC. The information contained in these documents cannot be released to third parties without the written consent of MC-21 LLC. Table of Contents Introduction .......................................................................................................................................... 7 General Information ............................................................................................................................. 7 2.1. About the Pharmacy Providers Manual ................................................................................................ 7 2.2. Contact Us ............................................................................................................................................. 8 Contact Information ............................................................................................................................. 8 3.1. MC-21 Offices ....................................................................................................................................... 8 3.2. Pharmacy Network (Credentialing and Re-Credentialing) .................................................................... 8 3.3. Pharmacy Network Call Center ............................................................................................................. 9 3.4. Prior Authorization (PA) Call
    [Show full text]