Fda And Regulations Of Medication Essay

1277 words - 6 pages

Demographic Paper
Tiearia Fariss
HCS/490
March 20, 2014
Professor Erika Johnson

It is economically correct to state that any baby that is born the life cycle will eventually age the individual. In today’s era the life expectancy for individual is a lot longer due to the advancements in technology, increased knowledge in medicine and treatments available, and the ever growing resources that are available to caregivers. The healthcare industry today has had several changes such as the concern for resources, the possible challenges that are on the rise for the growing elderly population.
Between 1900 and 2000, life expectancy in the U.S increased from 51 to 80 years for women and from ...view middle of the document...

In the event that the elderly health care consumers do not have family to provide emotional, physical, or financial support they will require additional assistance which can be quite costly. Without the necessary resources to manage chronic disease there is little chance of achieving a health quality of life. Managing chronic illness is one of the biggest challenges for the elderly population. Medication used to manage chronic illnesses can be very expensive and many of them are not covered by Medicare posing a debated issue that continues to receive publicity. Bottom line is that the elderly have decreased incomes and are being forced to either pay for multiple medications or deal with a less productive quality of life. Caregivers are often not able to assist with the growing cost of medications because they are likely already losing time at work to care for their family member. The annual cost for a patient with diabetes to receive medication is $1379, heart disease is $1187, and hypertension is $1029 (National Academy on an Aging Society, 2002). Financial burden is only one of the challenges related to the ever growing elderly population. There is also the need to ensure a focus on quality of life. Health care providers (professional and related) can help to ensure a more productive end of life experience to be had by all.
The focus has always been to treat the disease and while this makes perfect sense it is not enough anymore. There needs to be a strong focus on quality of life for the elderly to encourage a productive management of chronic illness and other end of life health issues that may occur. The term nursing home often causes a sense of fear and isolation when considered for a means of monitoring care and ensuring assistance for the elderly. To avoid having to use nursing homes so regularly society’s care givers both professional and otherwise should focus on a patient’s abilities to care for themselves. Should they be able to properly take care of themselves there needs to be a delivery of knowledge to encourage independence. Providing the elderly population with outreach programs and activities that meet their abilities can make the difference between an independent older adult and a nursing home candidate. It seems that some of the individual focus and family coaching in behavioral, financial, and physical activities and choices has been lacking in the health care delivery system because the focus has been to treat with a decreased effort to educate and provide alternate resources as well.
Chronic disease wellness programs are one way for society, patients, and the community to actively address the challenges related to the increasing elderly population. Through the use of these programs the elderly are encouraged to keep active, they are instructed on ways to prevent falls that might lead to difficulty remaining independent, there are nutritional and diet...

Other Essays Like Fda and Regulations of Medication

Merck and Company: Vioxx Essay

571 words - 3 pages Merck and Company recently pulled its arthritis medication, Vioxx, off the shelves because of recent studies that link the drug to increased risk of heart attack and stroke. The FDA had been conducting a study that showed an increased amount of cardiovascular problems in those who had been using Vioxx for eighteen months or more. This decision has outraged many Vioxx users because many had no idea of the newfound risks associated with Vioxx

Gm520: Legal, Political, and Ethical Dimensions

767 words - 4 pages be sure it takes the reader to the actual regulation). (10 points) The FDA or also known as the Food and Drug Administration are agencies that control the rules and regulations. I decided to use this agency as my reference because the FDA is one the most popular and important agency. This proposed regulation change who filed this petition with the FDA to amend their rule is Cargill. Scientist and researchers in Cargill research and development

Drug Abuse

5169 words - 21 pages provide education on new methods of safe and effective drug return and disposal. (ONDCP/ EPA/DEA/FDA/CDC/HHS/SAMHSA/NIDA) • Once DEA regulations have been established, engage PhRMA and others in the private sector to support community-based medication disposal programs. (ONDCP/FDA/DEA/HHS/CDC/ SAMHSA/EPA) IV. Enforcement Along with the increased legitimate use of prescription opioid medications in healthcare settings, there is also a small

Legal and Ethical Issues of a Medical Error Case

1063 words - 5 pages Administration (FDA) and the Institute for Safe Medication Practices (ISMP) state that some abbreviations, symbols and dose designations are frequently misinterpreted and lead to mistakes that result in patient harm (FDA, 2006). Therefore, it is the legal responsibility of the FDA, healthcare professionals, medical students, medical writers, and the pharmaceutical industry to eliminate the use of potentially confusing abbreviations in order to prevent cases

Administration of Medication

1024 words - 5 pages UNIT 4222 – 616 ADMINISTER MEDICATION TO INDIVIDUALS AND MONITOR EFFECTS Outcome 1 – Understand legislation, policy and procedures relevant to administration of medication 1 There are numerous Acts and Regulations that cover the administration of medication, these include - Health and Social Care Act Health and Safety at Work Act 1974 COSHH (Control of substances hazardous to health) Medicines Act 1968 stating a doctor

Administer Medication to Individuals and Monitor the Effects

1199 words - 5 pages cause them to feel ill or can be fatal. If medication is not taken and left out then others might misuse this too which is abuse. 5.7 Describe how to dispose of out of date and part-used medications in accordance with legal and organisational requirements. When an individual stops taking their medication then the home is left with out-of-date and part-used medication. Under the care home standards, the hazardous waste regulations and the

Chapter 44 Lecture Notes

2192 words - 9 pages information and prohibits them from making unsubstantiated health claims. Regulation of Drugs – The FDA had the power to regulate the testing, manufacture, distribution, and sale of drugs.  The FDA has devised a procedure for application and testing of new medicines, which might eventually lead to approval for distribution and sale. Business Ethics: Safety Warnings about Viagra  There are always risks involved in taking any medication.  Potential

Updated Herbal Supplement Regulations Needed

1697 words - 7 pages researched and tested like a regular drug before they trust what the label says? After all, turning to the back of a bottle and reading “This product has not been approved by the FDA” is not the most comforting statement. Even the FDA is proposing to amend their previous regulations and recommendations for both dietary supplements and food to make sure their information is as up-to-date as possible. By updating the nutrition information on product labels

Dick Butkus

698 words - 3 pages and Drug Administration The U.S. Food and Drug Administration (FDA) was formed in 1906. The FDA is an agency of the United States Department of Health and Human Services. It is responsible for safety regulations for most foods, dietary supplements, legal drugs, vaccines, biological medical products, medical devices, veterinary products, cosmetics, radiation-emitting devices, and blood products. They are also responsible for sanitation

Core Functions of Fda

2723 words - 11 pages ; there are necessary regulations and guidelines to ensure the purpose of the agency is being met. This paper will explore the needs, stakeholders, expected outcomes, and other regulatory action and implementation of the FDA. Introduction: The Food and Drug Administration Safety and Innovation Act (FDASIA) is a regulation which was proposed by The Food and Drug Administration (FDA or Agency) to establish a list of “qualifying pathogens” that are

Legal and Ethical Considerations in Marketing, Product Safety, and Intellectual Property

3049 words - 13 pages when in the business of providing consumable products to the public. Unfortunately, there are pharmaceutical corporations operating in the U.S. who are not abiding by the law and who are endangering public safety. Introduction This case study involves a pharmaceutical company that violated the intellectual property rights of a foreign nation; violated state compounding regulations, and violated product safety laws. The company established a

Related Papers

.Identify The Regulations Concerning Venipuncture, Drug Administration, And Iv Medication And How These Standards In Your Field

599 words - 3 pages 1.Identify the regulations concerning venipuncture, drug administration, and IV medication and how these standards in your field. The five rights (5 Rs) need to be followed when administering any medications: right patient, right medication, right dose, right time and the right route. Venipuncture procedure for the purpose of establishing peripheral venous access and for obtaining blood sample for laboratory tests follow the standards of

Health Literacy, Perceived Medication Benefits, Medication Adherence And Health Seeking Behaviour And Medication Adherence Among Patients With Chronic Illnesses Attending Primary Care In Rural...

779 words - 4 pages HEALTH LITERACY, PERCEIVED MEDICATION BENEFITS, MEDICATION ADHERENCE AND HEALTH-SEEKING BEHAVIOUR AND MEDICATION ADHERENCE AMONG PATIENTS WITH CHRONIC ILLNESSES ATTENDING PRIMARY CARE IN RURAL COMMUNITIES OF IKENNE LOCAL GOVERNMENT AREA, NIGERIA INTRODUCTION Background and Scope of the Study The main aim of any attempted remediation of a health problem of patients in a health system is to achieve certain desired health outcomes in the

Explain The Regulations And Requirements For Internal Quality Assurance In Own Area Of Practice

531 words - 3 pages 1.4 Explain the regulations and requirements for internal quality assurance in own area of practice As part of my role I have to follow college policies and procedures on a daily basis and I can access these at any time through the shared access area on the database in college. The main acts and rules that I need to follow in my area are: Health & Safety at Work Act (1974) Everyone has a responsibility for the safety of

Would Mandated Regulations For Bat Usage At All Levels Of Baseball Provide A Safer Environment For The Sport And Reduce Costs?

2068 words - 9 pages Would mandated regulations for bat usage at all levels of baseball provide a safer environment for the sport and reduce costs. Decades of debating over these questions leaves people in disagreement. When it comes to discussing the use of metal bats from Little League to the Majors cost, safety, and performance are among the currently most heavily debated topics, with wide spread disagreement among people in the industry. Complicating the