The nurse is discharging a client from the hospital who has a new prescription for furosemide. Which of the following client statements indicates an understanding of the teaching?
"I should limit my fluid intake while taking this medication."
"My blood pressure will increase while I am taking this medication."
"I should take this medication in the morning rather than at night."
"I should eat a diet low in potassium while taking this medication."
The Correct Answer is C
A) "I should limit my fluid intake while taking this medication":
This statement is incorrect. Furosemide is a loop diuretic that increases urine production to reduce fluid overload in conditions like heart failure or edema. It is essential for clients taking furosemide to maintain adequate hydration to prevent dehydration. Therefore, the client should not limit their fluid intake while taking this medication.
B) "My blood pressure will increase while I am taking this medication":
This statement is incorrect. Furosemide is primarily used to reduce blood pressure by promoting diuresis and reducing fluid volume. Therefore, it is unlikely that blood pressure would increase while taking this medication.
C) "I should take this medication in the morning rather than at night":
This is the correct answer. Furosemide is usually taken in the morning to prevent nocturia (excessive urination at night), as it can increase urinary frequency. Taking it earlier in the day allows for better fluid balance during waking hours and reduces the need to wake up frequently during the night to urinate.
D) "I should eat a diet low in potassium while taking this medication":
This statement is incorrect. Furosemide can cause potassium depletion as a side effect, so clients may be advised to consume potassium-rich foods or supplements unless contraindicated due to other medical conditions. However, it is not necessary to eat a diet low in potassium while taking furosemide unless specifically instructed by a healthcare provider.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is ["32"]
Explanation
Find the concentration of heparin in the solution:
Total heparin (units): 25,000 units
Volume of solution (mL): 500 mL
Heparin concentration (units/mL) = Total heparin (units) / Volume of solution (mL)
Heparin concentration (units/mL) = 25,000 units / 500 mL = 50 units/mL
Set up the flow rate equation:
Desired heparin infusion rate (units/hr): 1600 units/hr
Heparin concentration in solution (units/mL): 50 units/mL
Flow rate (mL/hr): We need to solve for this
Flow rate (mL/hr) = Desired heparin infusion rate (units/hr) / Heparin concentration (units/mL)
Calculate the flow rate (mL/hr):
Flow rate (mL/hr) = 1600 units/hr / 50 units/mL = 32 mL/hr (round to nearest whole number as requested)
Therefore, the nurse should set the IV pump to deliver approximately 32 mL/hr.
Correct Answer is A
Explanation
A) Excretion:
This is the correct answer. The kidneys play a crucial role in the excretion of drugs and their metabolites from the body. After drugs undergo metabolism in the liver or other tissues, the resulting metabolites are often water-soluble and can be filtered by the kidneys into the urine. This process helps eliminate drugs and their byproducts from the body, preventing their accumulation and potential toxicity.
B) Absorption:
Absorption refers to the movement of drugs from the site of administration into the bloodstream. While the kidneys do not directly facilitate drug absorption, they may indirectly influence drug absorption by regulating blood flow and systemic circulation.
C) Metabolism:
Metabolism, or biotransformation, involves the enzymatic alteration of drugs into metabolites, which are often more water-soluble and easier to excrete. While the liver is the primary site of drug metabolism, the kidneys do not play a direct role in drug metabolism.
D) Distribution:
Distribution refers to the movement of drugs from the bloodstream to various tissues and organs in the body. While the kidneys do not directly influence drug distribution, changes in renal function can affect drug distribution by altering blood flow and plasma protein binding. However, the primary role of the kidneys in pharmacokinetics is excretion, not distribution.
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