Lack of education, access to proper health care, and low income or poverty are some of the social determinants that affect the prevalence of STDs.
These can be elaborated as:
Lack of education - People are not properly educated on the implications and measures to prevent STDs (sexually transmitted diseases), leading to widespread infection.
Lack of access to proper health care - Improper or compromised health services is one of the main reasons for the increased cases of STDs as it fails to provide complete treatment for the disease.
Poverty - People may not have access to different safety mechanisms to avoid STDs due to their low income which can lead to an increase in infections in society.
There can be various social determinants apart from the ones mentioned above.
Learn more about sexually transmitted diseases here :
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Answer:
It would not be advisable to promote a product before they approve it since you do not know if they will validate it and you will spend on marketing for pleasure
Whether or not a new drug requires approval The FDA's dependence on the new drug fits an over-the-counter (OTC) monograph. OTC monographs specified conditions under which the FDA has predetermined that a medication will be safe and effective. Once an OTC monograph is finalized, medication devices can market OTC medications that conform to the monograph without FDA approval. The FDA also uses the application at its discretion to allow certain medications to be marketed without approval if they conform to tentative final monographs.
If a new medication does not meet a monograph, it will require FDA approval. To obtain FDA approval, drug manufacturers must conduct laboratory tests, animal and human clinical analyzes, and submit their information to FDA. The FDA will review the information and may then approve the medication if the agency determines the benefits of the medication plus the risks to the intended use. Marketing a new drug that is not compliant with an OTC monograph and without an FDA test is considered as marketing a new unapproved medication, which is a prohibited act under the Food, Drug and Cosmetic Act (FD&C Act).
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