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Wilkes NSG 533 Exam 1 Advanced Pharmacology 2025, Pass with Confidence.

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Wilkes NSG 533 Exam 1 Advanced Pharmacology 2025, Pass with Confidence. Prepare effectively for the 2025 Wilkes University NSG 533 Exam 1 with this comprehensive Advanced Pharmacology study guide. Designed specifically for graduate nursing students, this resource covers foundational pharmacological concepts including drug classifications, pharmacokinetics and pharmacodynamics, patient-centered medication administration, therapeutic uses, potential adverse effects, and clinical considerations. Highlighting evidence-based practice and safe medication management, it equips students with the essential knowledge and critical thinking skills needed to excel on Exam 1 and enhance clinical decision-making. With clear explanations, organized content, and targeted review questions, this guide is an essential tool for Wilkes NSG 533 students aiming for academic success and proficient pharmacology practice. --- Wilkes NSG 533 Exam 1 Advanced Pharmacology, NSG 533 pharmacology exam 1 study guide, Wilkes University NSG 533 exam 1 pharmacology review, NSG 533 nursing pharmacology exam 1 prep, Wilkes NSG 533 medication management exam 1, NSG 533 exam 1 pharmacology practice questions, Wilkes graduate nursing pharmacology exam 1, NSG 533 advanced pharmacology notes exam 1, Wilkes NSG 533 nursing exam 1 drug study, advanced pharmacology Wilkes NSG 533 exam 1

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Written in
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NSG533 / NSG 533 EXAM 1
Advanced Pharmacology - Wilkes
Actual Questions and Answers

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This Exam contains:

Grade A+ Wilkes

100% Guarantee Pass.

Each Question Includes The Correct Answer

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1/ 24

,1. EP is a 38-year-old female patient that comes in for diabetes education
and management. She was diagnosed 12 years ago and states lately she
is not able to control her diet although she continues a 1600 calorie diet
with appropriate daily carbohydrate intake (per dietitian prescription) and
walks 40 minutes every day of the week. She states compliance with all
medications.
She denies any history of hypoglycemia despite being able to identify
signs and symptoms and describe appropriate treatment strategies.
PMH: T2DM, HTN, obesity, depression, s/p thyroidectomy due to thyroid
cancer
FmHx: Noncontributory
SHx: () Smoking, alcohol use, past marijuana use while in high school
Medications: Metformin 850 mg tid, glipizide 20 mg bid, lisinopril 20 mg
daily, sertraline 100 mg daily, multivitamin daily
Vitals: BP 128/82 mg Hg; P 72 beats/min; BMI 31 m/kg2
Laboratory test results: Na 134 mEq/L, K 5.4 mEq/L, Cl 106 mEq/L, BUN
16 mg/dL, SCr 0.89 mg/dL, glucose 128 mg/dL; A1C 7.8%


Based on EP's profile above, which of the agents would be able to obtain
an A1C goal of less than 7% and would be appropriate in the patient?
Please pro- vide an explanation of appropriateness or lack thereof.:
Exenatide - Exenatide (Bydureon) once weekly has been able to demonstrate
weight loss and decrease A1C% by 0.7% to 1.2% in clinical trials; however it is
contraindicated for EP due to the self-reported history of thyroid cancer.
Dapagliflozin - Dapagliflozin (Farxiga) is contraindicated in this patient due to hy-
perkalemia which could be made worse by this drug. The package insert does not
indicate a specific potassium concentration cut off to no longer use this


,medication; however, there are better choices in this patient.
Sitagliptin - Sitagliptin (Januvia) is able to obtain an A1C goal of less than 7%
based on clinical trials and currently the patient does not have any cautionary
objective measures to not use this medication. DPP-IV inhibitors are weight
neutral. DPP-IV inhibitors can be used in patients taking sulfonylureas; however, it
may be recommended to reduce or stop the sulfonylurea dose.
Acarbose - Acarbose (Precose) is not recommended for initial management and
is associated with significant GI side effects. More information would be needed
regarding fasting and post-prandial numbers. In addition, adding acarbose
would only lower A1c by 0.8% at best and therefore would not achieve the
desired A1C goal of <7%


2. JR is a 68-year-old African American man with a new diagnosis of T2DM.
He was classified as having prediabetes (at risk for developing diabetes)
5 years before the diagnosis and has a strong family history of type 2
diabetes. JR's blood pressure was 150/92 mm Hg. His laboratory results
revealed an A1C of 8.1%, normal cholesterol panel, and normal
renal/hepatic function were noted with today's laboratory test results.
Past medical history: Hypertension (diagnosed 4 y ago) Hyperlipidemia
(diag- nosed 2 y ago) Pancreatitis (idiopathic) (acute hospitalization 3 y
ago) Family history: Type 2 diabetes
Medication: HCTZ 25 mg daily, simvastatin 10 mg daily
Allergies: SMZ/TMP
Vitals: BP: 150/92 mm Hg P: 78 beats/min RR: 12 rpm Waist
Circumference: 46 in Weight: 267 lb Height: 5 26 3BMI: 43.1 kg/m 2






, Despite improvements in the past six weeks due to lifestyle changes and
exercise, drug therapy is to be started for JR's diabetes. Which drug
therapy would be the best for JR to trial?
Discuss your opinion of JR's lipid management.
Discuss your opinion of JR's blood pressure management.: Metformin is the
drug of choice recommended for most patients with diabetes in addition to
lifestyle modifications assuming no contraindications or intolerabilities are present
upon evaluation. Metformin has also shown to provide positive weight neutral/loss
effects in obese patients. It is crucial to know the renal status of patients
commencing metformin therapy to limit the risk of lactic acidosis (JR is without
contraindication). Since his entry A1C is >7.5%, dual therapy is indicated. There
are several potential choices. The second step can be a dipeptidyl peptidase-4
inhibitor, it can be a glucagon-like peptide-1 (GLP-1) receptor agonist, it can be a
TZD, it can be a sulfonylurea agent, it can be a SGLT2 inhibitor, or it could be basal
insulin. Anything next can be tried depending on what suits the circumstance
DPP4 inhibitors are weight neutral bet relatively benign side effect profile.
Sitagliptin has been associated with case reports of pancreatitis, so this specific
agent should be avoided. $$$
GLP-1 analog and has data to support an A1C reduction necessary to gain glycemic
control and may assist with weight loss goals for this patient. New information
sug- gests these agents may provide benefits in those with ASCVD. JR has a past
history of pancreatitis and GLP-1 analogs are not recommended due to this
contraindication TZDs have data to support an A1C reduction necessary to gain
glycemic control, but are associated with weight gain, negative effects on lipids
and increased risk of fracture. Until recently, TZDs have also been linked to
increased CV events and use has fallen out of favor

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