No! Vaccines for Animal Illnesses: Vaccines for animal diseases are not regulated by the FDA. The US Department of Agriculture regulates veterinary biologics, including vaccinations for animal illnesses. These vaccines must be shown to be safe and effective before they can be sold in the United States.
However, there is an extensive system in place to monitor vaccine safety. Doctors and scientists review the data about the side effects of each vaccine as it is being developed. If a problem is identified, the manufacturer is required to update its labeling or take other action before putting a product on the market.
In addition, all drugs need to be proven safe before they can be put on the market. But because vaccines are only used under certain conditions and only give people a small amount of the toxic ingredient (the active substance), they can be considered safer than many medications. This is especially true for children, who often receive several vaccines at one time in relatively high doses. The risks associated with these treatments can be reduced by keeping vaccine schedules consistent from year to year and by waiting until a child is fully immune-competent to give him or her vaccines.
The only vaccine that has been linked to autism is the measles, mumps, and rubella (MMR) vaccine. However, this link has been controversial and cannot be confirmed without further study.
Food (except for portions of some meat, poultry, and egg products, which are controlled by the US Department of Agriculture); human and veterinary pharmaceuticals; vaccines and other biological goods; medical equipment intended for human use; radiation-emitting electronic devices...
Even though food is not regulated by the FDA, anyone who manufactures, imports, or sells foods must be licensed by the Food License Bureau. The license requires that they comply with federal safety standards but does not otherwise control how they operate their business.
The FDA also does not regulate: products that are manufactured or processed outside the United States; most herbs, spices, and flavors; many types of food supplements; some animal products; some industrial chemicals; and some medical devices.
In addition, the FDA does not inspect factories or corporate offices, and it cannot require companies to report chemical leaks or other environmental hazards. That responsibility falls to the U.S. Environmental Protection Agency (EPA) or other agencies.
However, the FDA does review new drugs and medical devices before they are sold in America. It also has the authority to take action against manufacturers who make false statements about their products on package labels or website reviews.
Finally, the FDA plays an important role in helping the public understand what substances are in foods and how they are used safely.
The FDA's involvement The FDA controls foods other than meat and poultry products controlled by the USDA, as permitted by the federal Food, Drug, and Cosmetic Act and the Public Health Service Act. The FDA is also in charge of medicine, medical device, biologics, animal feed, pharmaceuticals, cosmetics, and radiation-emitting equipment safety. It also has jurisdiction over chemical substances used in food or drug manufacturing.
FDA regulations are the highest level of protection for consumers who use their judgment rather than relying on government warning labels or artificial ingredients found in many processed foods. The agency requires that all food sold in the United States be proven to be safe for human consumption before it can be marketed. The agency also ensures that contaminated food is removed from store shelves.
In addition to regulating food manufacturers, farmers, ranchers, and fish farmers; handlers of imported food; and distributors/sellers of prepared food; they also monitor restaurant compliance with health standards. Finally, they provide consumer information on how to choose safe foods and avoid food hazards.
Through research and development, inspection, and coordination with other agencies, the FDA works to prevent contamination of food supplies. They do this by requiring those who produce or import foods to ensure that them is safe before it reaches market, by taking action against companies that violate safety rules, and by providing information on what foods should be kept away from children and others at risk for eating problems.
The FDA uses several methods to inspect businesses.
Drug makers must undergo lab, animal, and human clinical testing and submit their findings to the FDA in order to obtain FDA clearance. The FDA will then analyze the data and decide whether or not to approve the medicine if the benefits outweigh the dangers for the intended usage. Testing is required at different stages of development for both new drugs and existing products that are changed significantly after initial approval.
The process can take several years from start to finish. Once a drug has been approved, it must be monitored for safety issues during its distribution period. Drugs that have proven dangerous for certain users or in specific situations can be banned later when more information is available. New drugs are also tested on animals before they are released to see how they affect different species so humans can be warned about possible side effects.
New drugs cannot simply be added to the market without testing first. They have to go through rigorous trials with large participant groups to ensure they are safe and effective. Without this process many people would be harmed before any benefits were realized.
Drugs are chemicals and like all other chemicals they can be toxic if used incorrectly or in excess. Some drugs are poisonous by themselves while others need to be combined with other substances to become active. This is why it's important to know the ingredients in each pill you take. Some drugs are toxic if they're taken by mouth whereas others are only harmful if injected directly into a vein.