Which of the following is not an effect of the drug isoflurane?

Correct Answer: A

Rationale: The correct answer is A: Elevated lipid levels. Isoflurane does not cause elevated lipid levels. Isoflurane is a general anesthetic that primarily affects the central nervous system, leading to effects like decreased respiratory function and increased blood flow to the brain. Nausea can also be a side effect of isoflurane due to its impact on the gastrointestinal system. However, there is no direct link between isoflurane and elevated lipid levels. Thus, choice A is the correct answer.

Correct Answer: B

Rationale: The correct answer is B: Hypotension. Prednisone toxicity typically causes hypertension, not hypotension. Prednisone can lead to increased blood pressure due to its sodium-retaining effects. Cataracts (A), Psychosis (C), and Acne (D) are all known side effects of Prednisone toxicity. Cataracts can form due to long-term steroid use, psychosis can occur especially at higher doses, and acne is a common skin side effect. Therefore, hypotension is the odd one out among the choices given.

Correct Answer: B

Rationale: Barbiturates are central nervous system depressants used to treat seizures, insomnia, and anxiety. However, they can worsen hypotension as they can cause vasodilation and decrease blood pressure. Choice B is correct because using barbiturates in hypotensive patients can lead to further lowering of blood pressure, potentially causing harm. Choices A, C, and D are incorrect as barbiturates are commonly used to treat seizures, insomnia, and anxiety, respectively, due to their sedative and anticonvulsant properties.

Correct Answer: D

Rationale: The correct answer is D: H antagonist. Drugs ending in the suffix (tidine) typically belong to the class of histamine H2-receptor antagonists. These drugs work by blocking the action of histamine on H2 receptors in the stomach, reducing the production of stomach acid. This is commonly used to treat conditions such as peptic ulcers and gastroesophageal reflux disease. Explanation of other choices: A: Antidepressant - Drugs ending in (pramine) or (ine) are more commonly associated with antidepressants. B: Protease inhibitor - Drugs ending in (navir) are typically protease inhibitors used in antiviral therapy. C: Beta antagonist - Drugs ending in (olol) are beta-blockers, which are used to treat conditions such as hypertension and heart disease, not related to (tidine) suffix.

Correct Answer: D

Rationale: The correct answer is D: Muscle wasting. Ibuprofen is primarily associated with gastrointestinal side effects like nausea, renal dysfunction, and anemia due to its effects on the stomach, kidneys, and blood. Muscle wasting is not a known direct effect of Ibuprofen toxicity. Ibuprofen is not typically linked to muscle-related issues, making choice D the correct answer.

Correct Answer: C

Rationale: Correct Answer: C (Isoniazid) Rationale: 1. Isoniazid is known to cause drug-induced hepatitis due to its hepatotoxic effects. 2. It can lead to liver inflammation, causing hepatitis as a reaction. 3. Regular monitoring of liver function tests is essential when using isoniazid. Summary of other choices: A. Valproic acid: Can cause hepatotoxicity but not specifically linked to hepatitis. B. Quinidine: Mainly known for cardiac side effects, not commonly associated with hepatitis. D. Ethosuximide: Primarily used for treating absence seizures, not typically associated with hepatitis.

Correct Answer: B

Rationale: The correct answer is B: Tachycardia. Atenolol is a beta-blocker that works by slowing down the heart rate, so tachycardia is not related to its toxicity. A: CHF can be exacerbated by Atenolol due to its negative inotropic effects. C: AV block can occur as Atenolol can further slow down the heart's conduction system. D: Sedative appearance can be a side effect of Atenolol due to its action on the central nervous system. In summary, tachycardia is not related to Atenolol toxicity because it decreases heart rate.

Correct Answer: C

Rationale: The correct answer is C: Antifungal. Drugs ending in the suffix (azole) are commonly used to treat fungal infections. The suffix indicates that the drug belongs to the azole class, which specifically targets fungal pathogens by inhibiting their growth. Therefore, a drug ending in (azole) is classified as an antifungal medication. Summary of other choices: A: H - Incorrect. There is no pharmacological relevance to the suffix (azole) in relation to the letter H. B: ACE inhibitor - Incorrect. Drugs ending in (pril) are commonly ACE inhibitors, not those ending in (azole). D: Beta agonist - Incorrect. Drugs ending in (ol) or (olol) are typically beta agonists, not those ending in (azole).

Correct Answer: D

Rationale: The correct answer is D: Distal convoluted tubule. Potassium-sparing diuretics, such as spironolactone, act on the distal convoluted tubule by blocking the aldosterone receptor, which leads to decreased sodium reabsorption and potassium retention. This mechanism helps to promote diuresis while preventing potassium loss. Choices A, B, and C are incorrect because potassium-sparing diuretics do not primarily affect the proximal convoluted tubule, loop of Henle, or collecting duct in the kidney.