Ondansetron is effective in the following types of vomiting except:

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Chapter 11 principles of pharmacology Questions

Question 1 of 5

Ondansetron is effective in the following types of vomiting except:

Correct Answer: C

Rationale: In the context of pharmacology, understanding the indications for specific medications is crucial for safe and effective patient care. In this case, the correct answer is C) Motion sickness. Ondansetron is a selective serotonin 5-HT3 receptor antagonist primarily used to prevent nausea and vomiting caused by chemotherapy, radiation therapy, and post-operative procedures. Option A, Radiation-induced vomiting, and Option D, Vomiting caused by cytotoxic drugs, are both correct indications for ondansetron due to its mechanism of action in blocking serotonin receptors in the chemoreceptor trigger zone. Option B, Post-operative vomiting, is also a correct indication as ondansetron helps in reducing post-operative nausea and vomiting by its antiemetic properties. Option C, Motion sickness, is the exception as ondansetron is not typically used to treat motion sickness. Antihistamines like dimenhydrinate or meclizine are more commonly prescribed for motion sickness due to their mechanism of action in the vestibular system. Understanding the specific indications for ondansetron and other medications is essential for healthcare professionals to make informed decisions regarding patient treatment and medication management.

Question 2 of 5

Cross MATCH each drug to the most suitable indication: Constipation with low frequency of defecation

Correct Answer: D

Rationale: In this case, the correct answer is D) Bisacodyl/ Caster oil. Bisacodyl is a stimulant laxative that works by increasing the movement of the intestines, thus helping to facilitate bowel movements. This mechanism of action makes it suitable for constipation with low frequency of defecation as it can help stimulate the bowel to promote more regular and frequent bowel movements. Now, let's discuss why the other options are incorrect: A) Loperamide is an antidiarrheal medication that slows down bowel movements. It is not suitable for constipation with low frequency of defecation as it would further reduce bowel movements. B) Paraffin oil is a stool softener that helps to lubricate the stool and ease its passage. While it can be helpful for constipation, it may not be the most suitable for low frequency of defecation. C) Bran/ milk of magnesia are commonly used for constipation relief, but they work differently from Bisacodyl. Bran adds bulk to the stool, while milk of magnesia is an osmotic laxative that draws water into the intestines to soften the stool. These mechanisms may not directly address low frequency of defecation. In an educational context, understanding the mechanisms of action of different laxatives is crucial for selecting the most appropriate treatment based on the specific symptoms presented by the patient. It is important to consider not only the type of laxative but also how it works in the body to achieve the desired effect. This knowledge helps healthcare professionals make informed decisions to provide effective and tailored care to patients with gastrointestinal issues.

Question 3 of 5

Cross MATCH each drug to its specific adverse effect: Bran/Psyllium

Correct Answer: A

Rationale: In this question, the correct match is Option A) Intestinal obstruction if not taken with plenty of fluids. Bran/Psyllium is a type of fiber supplement that absorbs water in the intestines to create a bulky stool, which helps in regulating bowel movements. If not taken with plenty of fluids, Bran/Psyllium can swell and potentially cause intestinal obstruction due to its ability to absorb water and expand in the digestive tract. This adverse effect is directly related to the mechanism of action of Bran/Psyllium in the body. Now, let's analyze why the other options are incorrect: B) Mutagenic: Bran/Psyllium is not known to have mutagenic properties. It is a natural fiber supplement derived from plant sources and does not cause genetic mutations in cells. C) Lipid pneumonia: Bran/Psyllium is not associated with lipid pneumonia. This condition typically occurs when lipids enter the lungs, causing inflammation and respiratory issues. Bran/Psyllium is not a lipid-based substance and does not pose a risk for lipid pneumonia. D) Flatulence & aggravation of diabetes: While Bran/Psyllium may cause flatulence in some individuals due to its fiber content, it is not directly linked to aggravating diabetes. In fact, the soluble fiber in Bran/Psyllium can help in managing blood sugar levels in diabetic patients by slowing down the absorption of sugar. Educational Context: Understanding the adverse effects of medications and supplements is crucial in pharmacology to ensure safe and effective patient care. Students need to grasp the specific adverse effects of drugs to make informed decisions about their use in clinical practice. In this case, linking Bran/Psyllium to the potential adverse effect of intestinal obstruction reinforces the importance of proper administration and patient education when prescribing fiber supplements.

Question 4 of 5

All the following are involved in the mechanism of action of morphine Except

Correct Answer: A

Rationale: In the context of pharmacology, understanding the mechanism of action of drugs is crucial for healthcare professionals. In the case of morphine, it is important to grasp how it exerts its effects to ensure safe and effective patient care. The correct answer is A) Most effects are mediated by activation of kappa receptors. Morphine primarily exerts its analgesic effects through the activation of mu-opioid receptors, not kappa receptors. While there may be some involvement of kappa receptors in certain effects of morphine, it is not the main mechanism of action. Option B) Inhibition of calcium influx resulting in inhibition of transmitter release is a plausible mechanism for opioids like morphine in reducing neurotransmitter release and subsequently modulating pain perception. Option C) Increase in K outflux resulting in hyperpolarization of neuronal membrane is a valid mechanism for opioids like morphine in reducing neuronal excitability and pain transmission. Option D) Reduction of emotional response to pain is also a recognized effect of opioids like morphine due to their action on the central nervous system. Educationally, this question highlights the need for students to differentiate between the various mechanisms of action of drugs and understand the primary targets through which a drug exerts its effects. It emphasizes the importance of precision in pharmacological knowledge to make informed clinical decisions and ensure optimal patient outcomes.

Question 5 of 5

The following is not common between pethidine & buprenorphine :

Correct Answer: B

Rationale: In this question comparing pethidine and buprenorphine, the correct answer is option B, which states that respiratory depression is not increased by increasing the dose. This is a key difference between these two drugs. Pethidine, also known as meperidine, is a traditional opioid analgesic that can cause dose-dependent respiratory depression. In contrast, buprenorphine is a partial opioid agonist with a ceiling effect on respiratory depression, meaning that increasing the dose beyond a certain point does not lead to a proportional increase in respiratory depression. Option A is incorrect because both pethidine and buprenorphine have analgesic effects in severe pain, although buprenorphine is more commonly used for chronic pain management. Option C is incorrect as both drugs can cause nausea and vomiting as common side effects. Option D is incorrect as both drugs can also cause constipation, which is a common side effect of opioid medications. In an educational context, understanding the differences between opioid medications like pethidine and buprenorphine is crucial for healthcare professionals managing pain in patients. Knowing the specific characteristics of each drug, including their side effect profiles and unique pharmacological properties, helps in making informed decisions about the most appropriate treatment for individual patients based on their clinical needs and risk factors.

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