ipl-logo

Preliminary Health Claims Essay

615 Words3 Pages

The difference between “Solid Health Claims” and “Preliminary Health Claims” is the level of evidence to support the claim. “Solid” claims are supported by solid evidence, and suggest certain diets that are high or low in specific nutrients may help prevent a specific disease. “Preliminary” health claims do not have solid evidence, and instead are based off of “incomplete, shaky evidence.” The food industry is likely to disregard both of these types of claims in favor of a “structure/function” claim which are completely unreliable, and make broad suggestions about the body’s functions with vague terminology that means almost nothing. They favor this type of claim because it requires close to zero approval from the FDA, and unsuspecting consumers will be convinced by the claim and spend money on …show more content…

However, some products, such as specific vitamins, are well-tested to prove beneficial in some aspects, yet manufactures do not have the time to wait for FDA approval because of the competitive market. These same manufacturers could also be providing a cheap form of that vitamin that is not absorbed by the body, and they attempt to hide that from the customer. I feel that these claims can be dangerous, but not on their own. It takes an ignorant, gullible, and desperate person to be negatively impacted by these claims. If someone is diagnosed a real disease and needs to take real medicine for it, but they head over to the Vitamin Shoppe instead because of some structure/function claim on a pill bottle, then that would be dangerous because they would be lacking the proper treatment. There is also the possibility that a supplement is not well-tested, and could be causing unknown harm to the consumer. In general, it is probably a bad idea to be putting things in your body that have not been confirmed to be universally

Show More
Related
994 Words | 4 Pages

i.10The sponsor is providing the minor with a safe environment. The placement is located in an apartment complex in Woodbridge, VA. The placement appears to be safe and no visible hazards were observed. The minor is provided her own bed and shares the bedroom with other sisters. The minor did not report any concerns regarding her safety, the placement or the community.

Read More
1847 Words | 8 Pages

In Pearson v. Shalala, when appellant tried to validate the health claims as per the procedure for evaluating the validity of health claims for the dietary supplements (21 CFR section 101.7), the FDA denied to include the four health claims on the labels for the dietary supplements marketed by Mr. Pearson and Mr. Shaw11. The FDA deemed that the claims lack the significant scientific agreement standard because the evidence provided for approval includes the research that examines the relationship between consumption of foods containing the components of dietary supplements and the risk of the diseases. On that basis, the FDA determined that the specific effect of the dietary supplement components could not be determined with certainty11. Along with that, the government disputed that the appellants proposed health claims could create confusion among the consumers11. In response to this, the appellant argued that their First Amendment rights have been impaired as under Administrative Procedure Act because the FDA was required to provide

Read More
715 Words | 3 Pages

I do agree that companies who create such products that easily cause harm to people should have some sort of action taken against their use but to that extent, I say that the companies also have to specify how much to use and when the consumption of their products becomes too much. However, the precedences for more positive descriptions of that side of the topic are a lot more complicated to explain and as such my view starts to hit a wall and I will now talk about how I disagree with Coffman 's claims. First off, Coffman makes it seem that the companies who produce legal but harmful products, which in its own right can be taken multiple ways, should pay settlements for the problems caused by their products. The problem with claims like this is that when a company makes a product they have normally created it for a specific purpose and have set in place guidelines to prevent potential harm, an example of a type of product like this would be aspirin which is commonly used as a pain reliever in the form of pills but can cause harm if too many are

Read More
256 Words | 2 Pages

The Food and Drug Administration (FDA) was given control to regulate dietary supplements in 1994 when the Dietary Supplement Health and Education Act was passed. Although dietary supplements are not classified as “drugs,” the FDA monitors them in different ways such as manufacturing, price, purity and labeling. Conversely, the FDA is not permitted to ensure that the supplements are effective before being placed on the market. The FDA is only able to remove the product off of the shelf if they are able to prove that the supplement is unsafe, show that structure- function claims are untrue, or after injuries have been reported. While manufacturers are not required to disclose information about the authentication of structure- function claims,

Read More
507 Words | 3 Pages

Healthcare Options – (HRA) Health Reimbursement Accounts Health Reimbursement arrangement (HRA) is an employer-funded medical reimbursement plan for employees. Health Reimbursement accounts is designed by the Internal Revenue Service (IRS) to enable employers reimburse their employees for certain medical expenses. This helps the employee settle the cost of their medical expenses. Additionally, it also help the employer save money on taxes. Who can benefit from Health Reimbursement arrangements?

Read More
469 Words | 2 Pages

I should be considered for the Kaiser Permanente Health Care Scholarship because I have proved and accomplished more than what I thought I would be capable of in my education, I am passionate for the health industry, and I financially need to be to succeed. I will continue my education by pursuing my goal to become a Registered Nurse. I first considered Registered Nursing when I joined the Health Academy and realized how passionate I was to help others. Throughout my years in the Health Academy, my passion grew drastically. My summer of 2015 was dedicated to two internships; one being a Medical Assistant (200 hours) and another as a Physical Therapy Aide (80 hours).

Read More
772 Words | 4 Pages

Changes are regularly being monitored by the NHS to ensure its policies, legislation, regulations and codes of practice are suitable and precise to the changing ethnic, financial and cultural backgrounds of the population. The health and Social Care Act 2012 stands as the most common legislation guiding the health and social care field within the UK. It offers for the most widespread reorganization of the structure of the National Health Service in England. It allows policies for managers within the health and social care sector, professional responsibility which will empower them.

Read More
3686 Words | 15 Pages

According to the CDC “The Health Insurance Portability And Accountability Act of 1996 was created to protect sensitive patient health information from being disclosed without the patient's consent or knowledge”. (Public Health Professionals Gateway, para 1, 2022). The Health Insurance Portability and Accountability Act is a federal law that requires the creation of national standards to protect sensitive patient health information from being disclosed without authorization. The importance of this keeps employees from having job-lock or from consequences from the terrible aftermath of a situation. Furthermore, it provides standards for individual rights to make an understanding and learn how to control how their health information is used.

Read More
315 Words | 2 Pages

The Medical Necessity Defense Many countries have not legalized marijuana use for medicinal purposes and, in those states, putting forward a medical necessity defense may be necessary. The basis necessity defense, also recognized as the "choice of two evils" was available to those who, when faced with a grave and immediate threat, found they could redeem themselves only by demanding action that violated a law. FN33 The medical necessity defense was established for marijuana in United States v. Randall FN34 in which a glaucoma patient who smoked marijuana in order to retain his eyesight was found not guilty of violating anti-marijuana law by the District of Columbia Superior Court. Knowing "the right of an individual to keep and manipulate

Read More
485 Words | 2 Pages

When you get injured on the job or you believe an injury is due to your work, it is important to file a workers compensation claim immediately. Certain states have a time frame in which you need to file the claim in order for it to be valid. Once you file a claim, this does not mean that this is all that you need to do. After filing the initial claim, the workers compensation office will need you to provide material to support your claim. This involves a lot of paperwork that can easily become overwhelming if you are unable to stay on top of it.

Read More
505 Words | 3 Pages

Supplements like these offer a safe and inexpensive way to see great gains, with none of the

Read More
1283 Words | 6 Pages

Therefore, leading to a very big lawsuit. (Negowetti pg. 13-15) There is a very blurry line for defining what an actual “natural” product is. In order to clear up the blurriness around the definition of “natural” the FDA has defined what it means; for consumers and companies to have a better understanding of the term “natural”.

Read More
1866 Words | 8 Pages

Dear FAA Medical Certification Division, 1. A detailed statement from you detailing the frequency of your past and present substance and alcohol use/abuse. I first smoked pot when I was 12 years old. My mother used marijuana, to relax and cope with the stresses of life.

Read More
1055 Words | 5 Pages

The same thing applies to Vitamin D pills, till now no one knows what amount is safe and an overdose would lead to HyperCalcemia , which produces Kidney stones, meddles with your heart and brain, and damages your bones. Still, Vitamin D experts are increasing the daily amount needed well aware of the risks. So, some people opt for what they consider the safest way to get Vitamin D – Food. Vitamin D is commonly found in Dairy products , fatty fish, orange juice , egg yolks…etc. Nevertheless, one requires

Read More
700 Words | 3 Pages

Being formed in 1948, the Universal Declaration of Human Rights helps recognize “the inherent dignity” and the “equal and unalienable rights of all members of the human family”. Based on this very concept of the person, and the fundamental dignity and equality of all human beings, that the notion of patient rights was developed. Patient rights involve those basic rules of conduct between patients and medical caregivers as well as the institutions and people that support them. A patient is anyone who has requested to be evaluated by or who is being evaluated by any healthcare professional.

Read More

More about Preliminary Health Claims Essay

Related Topics

Open Document