Drugs fulfill to the needs and requirements of primary healthcare of population are called as essential drugs, which are available in adequate amounts, in the appropriate dosage forms with assured quality and detailed information providing evidence on efficacy and safety, and comparative cost effectiveness. The Alma-Ata declaration during the International Conference on Primary Health Care in 1978 reaffirms that health is a fundamental human right and the attainment of the highest possible level of health is a most important worldwide social goal. The Alma Ata declaration has outlined the eight essential components of primary health care and provision of essential medicines is one of them (1). Management of essential medicines results in a …show more content…
WHO criteria to guide selection of an essential drug (4)
1. From clinical data available globally drugs safety and efficacy should be determined.
2. Taking in to the consideration of factors such as treatment facilities available for the incidence and pattern of the disease, genetic, demographic factors and financial resources of the patient, including the technical expertise and environmental factors choice of drug is finalized.
3. When the more options of drugs available under a specific category choice should be made on the basis of relative efficacy, safety, quality, price and availability. Cost benefit ratio remains a major
…show more content…
Essential drug list doesn’t implicate that only these drugs are useful and others are not, but most of the cases majority of the population will be in a situation to be accessed to the most needed essential medicines list for the health care of the individuals
The impacts of essential drugs (5)
1. To help save lives and improve health by closing the huge gap between the potential that essential drugs have to offer and the reality that for millions of people – particularly the poor and disadvantaged - medicines are unavailable, unaffordable, unsafe or improperly used.
2. Have a profound health impact; effective drug treatment now exists for most leading infectious diseases. Essential life-saving drugs have also been developed for leading no communicable diseases such as ischemic heart disease and cerebrovascular disease. Essential drugs save lives and reduce suffering, especially for impoverished populations.
3. Essential drugs increase the credibility of a health system and promote patient participation.
4. Effective and transparent drug procurement increases the confidence of governments, ministries of finance and donors in a country's health
Healthcare professionals must talk to their patients about possible side-effects of drugs they are taking and make sure they understand what can happen. In doing so, patients may start to understand why something is happening to them and it is a normal side-effect, which can not only lead to trust from the patients to providers, but can lead to the passing of knowledge from one to another which may prevent future
The Orphan Drug Act of 1983 was signed for the main purpose of promoting the research, treatment, prevention and diagnosis of rare disease or condition. Here the products which are used in rare disease can be drugs, biologics and medical devices. A rare disease means any disease which affects less than 200,000 persons in the United States or one in which the manufacturer has no expectation of recovering the money from development and sales in the United States. According to this act, there are certain incentives will be provided to the manufacturers who will develop orphan drug for the rare disease and condition. Thus, this act can encourage the treatment for rare disease.
A new oral pharmaceutical drug for type- two diabetes had been approved for clinical use, it was called Compound 17392. Marketing companies instantly wanted to have prescribers adopt and sell the product and researchers wanted to further investigate previous reports of liver toxicity in patients. Now since paying patients to try new pharmaceutical drugs was an issue due to it appearing to interfere with clinical judgement and upholding the duty to do what is best for the patient, a new idea of furthering research for the drug came into play. The idea included recruiting a group of physicians who were in the top ten percent of prescribers for type-two diabetes. Following regulations put in place by researchers, these physicians were to enter eligible patients into the trial for Compound
As mentioned in Napoleons’ Button (Couteur and Burreson, 2003), ever since the discovery of penicillin, wound infection declines, saving plenty of lives, especially during the World War 2. The rapid advancement of drugs has indeed come a long way and even revolutionized the world. Drugs such as paracetemol helps to subside one’s fever and provide pain relief. On the other hand, drugs that are widely used illegally such as cocaine would be detrimental to one’s personal health when consumed. In any case, the mere existence of drugs is good in nature.
The outcome of attempting this would make it even simpler to gain a profit in the drug industry. In the author’s opinion, if the process to acquire drugs becomes simpler, then the number of individuals
Relevant Facts: Nurofen, the pain-relief medication is made by Reckitt Benckiser Australia, a multinational company. The company was found misleading customers for all its specific range that contained the same active ingredient ibuprofen lysine 342mg and was seen to have same effect. The product was advertised the products as been targeting back pain, period pain and tension headaches. The Company was fined $1.7m for misleading customers on range of ‘specific pain’ relief contravening Australian Consumer Law has been brought forward by ACCC. The ACCC had asked federal court to impose $6 million fine.
Assignment 1: Explicating arguments The article Marcia Angell wrote discusses the ethics of running clinical trials in areas of poverty such as third world countries. It is largely stressed that the well-being of participants should be the main priority of the study, above research goals and quick results. She explains that participants in clinical trials must receive the best-known treatment available when part of the control group; otherwise, researchers would knowingly be giving participants sub-par treatment compared to the drug being studied. To enact justice, even those living in third world countries should be receiving the same treatment that a participant in a first world country would receive.
(Rissmann et al., 2012). Hence, considering the aspect of patient, NMC has picked up a cue as it is used by pharmacists while helping them in advising people in order to buy medications. Thus, this aspect is not strong enough to go into isolation as if it is combined with the charge, which ensures that medication history is taken along with OTC, herbal, POMs, allergies since patients need to explain that these aspects need to explain that which aspect is essential. Hence, assessment of holistic needs of patient looks for the determinants of health. However, patients frequently omit to explain regarding the OTC preps plus the herbal needs, which also needs to explain the usage of contraindicated drugs as it all explains the illegal needs of the
Partnership in health care is important in order to provide the best care to the patients, especially with the involvement of the patient, who is the center of this joint partnership. In the perspective of medicines management both professionals have the same goal of assuring that the treatment of patient containing pharmacology interventions is safe and effective. This essay will look at the main principles supporting supplementary prescribing, the clinical management plan, the partnership and the implementation of supplementary prescribing. Supplementary prescribing was introduced in 2003 for nurses, midwives and pharmacists which were then extended to optometrists and allied health professionals such as physiotherapists, podiatrists/chiropodists
Today many countries try to regulate the numbers of drugs users as many as they can by using the scary promotions and commercials to attract the attention from people, albeit ineffective. Rather than using the outmoded methods, legitimacy should be announced for all drugs in order that the regulation will process more ease for the government. In this procedure, the government can legislate the limitations for drugs consumption and people will be able to understand drug disadvantages profoundly. Therefore, allowing drugs as ordinary substances will abate the drug consumption. The aforementioned issue, in brief, the drugs is a too danger to leave it as it is so it should be legalized.
At the time not even the most straightforward diseases, for example,not even the common cold was curable. Until the best medicinal disclosure at the time was accidently found in 1928. Starting its potential amid World War 2, the entire world needed its hands on it. It was Penicillin. Penicillin left an imprint in our history, it expanded medicinal innovation, manufacturing and even diminished diseases.
Drug Kardexes were gathered and audited under certain criteria in order to identify potential risk areas in drug prescribing and administration, and also to provide ways in which these risks can be reduced or eliminated and reinforce drug management policies’ and guidelines. NICE (2002) audit cycle will be applied to this assignment to provide an acceptable framework (Appendix 1). Step 1: Preparing for Audit. The first step in the audit process is to identify which type of audit is to be carried out.
It may surprise you that, according to the World Health Organization (WHO) and World Bank, at least 400 million people lack access to essential health services. They said, at least 6 percent of people in 37 low and middle income countries are living in poverty because they must spend the money for health. Health care services is the most importance thing that we need because it is not only for improve the health but also through individual behaviour and lifestyle choices such as quitting smoking, eating the nutritious food and living a healthy lifestyles.
Threat of substitutes (low): This is one of the great advantages of the pharma industry. Because the demand for pharma products continues and the industry flourish. One of the main reasons for high competitiveness in the field is that it is an ongoing
Many new companies to enter the market without burden of costly tasks such as research and development, clinical trials and manufacturing of drugs. Moreover, patent expiry is one of the reasons which is offering opportunities for lower cost generic manufacturer in terms of greater market access. Additionally, the government has increased their focus on healthcare cost cutting. It is creating pressure on the authority to allow early introduction of low-cost drugs in the