A prescription calls for 5 mg of morphine sulfate. Using a sensitivity requirement of 5 mg, how would you obtain the required amount of morphine sulfate with an error not greater than 5%?
100 mg of drug, 1900 mg of diluent, 100 mg of aliquot
150 mg of drug, 2250 mg of diluent, 100 mg of aliquot
125 mg of drug, 1675 mg of diluent, 80 mg of aliquot
120 mg of drug, 2000 mg of diluent, 100 mg of aliquot
80 mg of drug, 1920 mg of diluent, 80 mg of aliquot
The Correct Answer is A
Step 1 is to calculate the Least Weighable Quantity (LWQ)
LWQ = (Sensitivity Requirement ÷ Acceptable Error) × 100
(5 ÷ 5) × 100
5 ÷ 5 = 1
1 × 100 = 100
Result at this step = 100 mg
Step 2 is to determine the drug multiplication factor
Since the required dose is 5 mg and we must weigh at least 100 mg:
Factor = 100 ÷ 5
100 ÷ 5 = 20
Result at this step = 20
Step 3 is to calculate the total mixture weight (drug + diluent)
Total Mixture = Aliquot weight × Factor
100 × 20 = 2000
Result at this step = 2000 mg
Step 4 is to calculate the amount of diluent needed
Diluent = Total Mixture - Drug weight
2000 - 100 = 1900
Result at this step = 1900 mg
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is B
Explanation
Non-parametric tests are statistical tools used when data do not meet the assumptions of a normal distribution. These tests do not rely on parameters such as the mean or standard deviation of a population. They are often used for ordinal or nominal data or when the sample size is too small to assume normality. These methods provide a robust way to analyze data that is skewed or contains significant outliers.
Rationale:
A. The t-test is a classic parametric test used to compare the means of two independent groups. It assumes that the data follow a normal distribution and that the variances between the groups are equal. Because it relies on the calculation of a specific population parameter (the mean), it does not qualify as non-parametric. It is highly sensitive to non-normal data.
B. Chi-square test is the correct answer as it is a widely used non-parametric test for categorical data. it evaluates the difference between observed and expected frequencies rather than comparing means. It makes no assumptions about the underlying distribution of the population. This makes it ideal for analyzing proportions and associations between nominal variables in clinical research.
C. ANOVA (Analysis of Variance) is a parametric method used to compare the means of three or more groups. Like the t-test, it assumes normality and homoscedasticity (equal variance) across all groups being tested. It uses the F-statistic to determine if any group mean is significantly different. It is not suitable for data that violates parametric assumptions.
D. The paired t-test is a parametric procedure designed to compare means from the same group at two different times. It relies on the assumption that the differences between the pairs are normally distributed. Since it is a variation of the standard t-test using mean values, it is classified as parametric. It cannot be used for non-normally distributed dependent samples.
Correct Answer is A
Explanation
Albuterol is a sympathomimetic bronchodilator categorized as a short-acting beta-2 agonist (SABA). It selectively stimulates beta-2 receptors in the lungs to induce smooth muscle relaxation via adenylate cyclase activation. This increases intracellular cAMP levels, effectively reversing acute bronchoconstriction in asthma or COPD patients. Side effects commonly include tachycardia, tremors, and palpitations due to transient stimulation of beta-1 and skeletal muscle receptors.
Rationale:
A. ProAir HFA is the correct answer as it is a brand-name formulation of albuterol sulfate. It utilizes a metered-dose inhaler with hydrofluoroalkane propellant to deliver the medication directly to the bronchioles. This product is the gold standard for providing rapid relief of respiratory distress. It is frequently prescribed for exercise-induced bronchospasm and acute asthma exacerbations.
B. Primatene Mist contains epinephrine as the active ingredient, which is a non-selective alpha and beta-adrenergic agonist. While it provides bronchodilation, it lacks the beta-2 selectivity found in albuterol and has a higher risk of systemic cardiovascular stimulation. It is an over-the-counter medication and is not a formulation of albuterol.
C. Asthmanefrin contains racepinephrine, which is a racemic mixture of epinephrine. It is delivered via an atomizer but is not considered a SABA like albuterol due to its non-selective adrenergic profile. It is primarily used for temporary relief of bronchial asthma symptoms but does not contain the specific albuterol molecule.
D. Xopenex HFA contains levalbuterol, which is the (R)-enantiomer of albuterol. While structurally related, it is a purified form that removes the (S)-isomer, which is thought to be clinically inactive or potentially pro-inflammatory. Therefore, while it acts similarly, the active ingredient is levalbuterol, not racemic albuterol, making this choice technically incorrect.
E. Xopenex Concentrate is the nebulized solution form of levalbuterol. Like the HFA version, it specifically provides the single-isomer levalbuterol for inhalation therapy. It is used for patients who cannot effectively use a handheld inhaler or require high-dose therapy in a clinical setting. It does not contain standard racemic albuterol.
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