This type of data is spoken information that is given by the patient. In some instances, it is the patient and family's ability and willingness to take medications appropriately.
What is Subjective Data
What is evaluation
This role involves having a clear and active license.
What is provider of care
This the primary regulatory agency for drugs in the US. They also regulates agents that are classified as drugs.
Who is the Food and Drug Administration or FDA
This Act is determined by the state. This document protects the term Nurse and the scope of practice. Its requirements also protect public health.
This type of data involves the patients past medical history (PMH). It includes their medication history such as prescription and OTCs, herbal, illict drug use and allergies to medication.
What is Objective Data?
Under this circumstance, the nurse should take cognitive ability, communication, health benefits and learning style into consideration.
What is educating a patient with a knowledge deficit
This role involves recognizing problems, time management and even becoming a team leader
What is a manager of care
This agency regulates OTC, biological therapeutics and generic medications.
What is the Centers for Drug Evaluation and Research (CDER)
This area of resources involves the the medication administration record (MAR), pain level and medication errors
What is Documentation?
What is the North American Diagnosis Association
This instance involves having another licensed personal within the same scope of practice verify specific drugs such as insulin, drug calculations and drug strength and lethality.
What are special circumstances
This role involves staying current with ones understanding of their resources.
What is a member of the profession?
This center regulates biologic drugs such as vaccines
What is the Center for Biologics Evaluation and Research (CBER)
These standards are set by the American Nurses Association and establishes clinical practices.
What are the standards of care?
What is to identify and prioritize goals
These checks are done on the 1st contact with the medication, prior to opening the medication, and prior to administering the medication.
What are the three medication checks
Asking what went wrong and how to be proactive and preventing this mistake in the future can be applied to this.
What are medication errors
This center regulates safety for food and cosmetic regulations.
What is the Center for Food Safety and Applied Nutrition
This involves medication administration, combining, the patient's list of current medications and how to instruct the patient through utilization of materials and techniques
What is areas applicable to knowledge deficit
These rights include the patient identification, drug name, correct dose, correct route, time/frequency and proper documentation.
What are the 6 rights of medication administration
This patient right goes into effect when a patient makes the informed decision (after the provider has explained the consequences) to not take the medication.
This Act states that this area is not evaluated by the FDA. It requires the manufacturer to ensure consumer safety and prohibits them from making false or crazy claims. Hint: think supplements
Dietary Supplement Health and Education Act (1994)
This resources is provided by the department of health and human services and oversee health care programs such as these.
What is the Centers for Medicare and Medicaid Services?