Considerate design

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Holding a certification in a certain field definitely shows that one have a good command of the BPS-Pharmacotherapy knowledge and professional skills in the related field. However, it is universally accepted that the majority of the candidates for the Pharmacotherapy (Part1 and Part2) Exam exam are those who do not have enough spare time and are not able to study in the most efficient way.

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High pass rate

It is certain that the pass rate among our customers is the most essential criteria to check out whether our BPS-Pharmacotherapy training materials are effective or not. The good news is that according to statistics, under the help of our training materials, the pass rate among our customers has reached as high as 98% to 100%. Our training materials have been honored as the panacea for the candidates for the exam since all of the contents in the BPS-Pharmacotherapy guide materials: Pharmacotherapy (Part1 and Part2) Exam are the essences of the exam. There are detailed explanations for some difficult questions in our BPS-Pharmacotherapy exam practice. Consequently, with the help of our study materials, you can be confident that you will pass the exam and get the related certification as easy as rolling off a log. So what are you waiting for? Just take immediate actions!

Online app version available

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BPS Pharmacotherapy (Part1 and Part2) Sample Questions:

1. From ethical and scientific validity standpoints, in addition to double blinding, which of the following research designs is best for determining a new medication's relative efficacy in treating acute stroke?

A) Parallel design comparing the new therapy with the best standard therapy
B) Placebo-controlled, crossover design
C) Placebo-controlled, randomized, parallel design
D) Crossover design comparing the new therapy with the best standard therapy

2. What is the most appropriate source for identifying the generic name, classification, and adverse effects of a foreign brand-name medication?

A) American Hospital Formulary Service Drug information
B) Micromedex
C) Drug Facts & Comparisons
D) Martindale: The Complete Drug Reference

3. When low molecular weight heparin is prescribed, in which of the following patient populations would monitoring anti-factor-Xa levels be reasonable to consider?

A) Protein C and Protein S deficiencies
B) Anticardiolipin antibody syndrome
C) Significant renal impairment
D) Past history of GI bleeding

4. A 59-year-old patient who is HIV-positive is receiving darunavir and ritonavir as part of a highly active antiretroviral therapy program. Which herbal supplement is contraindicated for this patient because it would decrease darunavir concentrations?

A) St. John's wort
B) Saw palmetto
C) Echinacea
D) Kava kava

5. A study shows that the participants who received 6 months of a new oral anticoagulant after a venous thromboembolism were randomized to continue with the new oral anticoagulant (n =
612) or to placebo (n = 611) for 18 months. Thromboembolism recurred in 12 subjects in the new oral anticoagulant group and 71 subjects in the placebo group (hazard ratio 0.17; 95% CI, 0.09-
0.30; p < 0.001).
Which of the following statements regarding these results is correct?

A) The new oral anticoagulant reduces the relative risk of a secondary venous thromboembolism by 17% compared to placebo.
B) The new oral anticoagulant reduces the relative risk of a secondary venous thromboembolism by 9.6% compared to placebo.
C) The new oral anticoagulant reduces the relative risk of a secondary venous thromboembolism by 83% compared to placebo.
D) The difference between the new oral anticoagulant and placebo in the secondary prevention of venous thromboembolism is not statistically significant.

Solutions: