What is the antidote for copper toxicity?

Correct Answer: D

Rationale: The correct answer is D: Penicillamine. Penicillamine is a chelating agent that binds to copper and forms a complex that can be excreted from the body, making it an effective antidote for copper toxicity. Glucagon (A) is used for treating hypoglycemia, aminocaproic acid (B) is used to treat excessive bleeding, and atropine (C) is used to treat bradycardia and organophosphate poisoning, none of which are related to copper toxicity.

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: D

Rationale: The correct answer is D: Penicillamine. Penicillamine is a chelating agent that binds to copper and forms a complex that can be excreted from the body, making it an effective antidote for copper toxicity. Glucagon (A) is used for treating hypoglycemia, aminocaproic acid (B) is used to treat excessive bleeding, and atropine (C) is used to treat bradycardia and organophosphate poisoning, none of which are related to copper toxicity.

Correct Answer: C

Rationale: The correct answer is C: Sedation. Opioid analgesics like dextromethorphan and methadone are primarily used for pain management, not sedation. They work by binding to opioid receptors in the brain to reduce pain perception. Pulmonary edema can be managed with diuretics, cough suppression with antitussives, and sedation with sedatives/hypnotics. Therefore, sedation is not a condition typically treated with opioid analgesics.

Correct Answer: D

Rationale: The correct answer is D: Sexual dysfunction. Nifedipine is a calcium channel blocker that primarily causes vasodilation by relaxing blood vessels. Sexual dysfunction is not a common side effect associated with Nifedipine use. Nausea, flushed appearance, and vertigo are potential side effects of Nifedipine due to its mechanism of action on the cardiovascular system. Therefore, D is the correct choice as it does not align with the expected side effects of Nifedipine.

Correct Answer: B

Rationale: The correct answer is B: Quinidine. Cinchonism is a condition caused by the toxicity of Cinchona alkaloids, which are found in drugs like quinine and quinidine. Quinidine is specifically known to cause symptoms of cinchonism such as tinnitus, headache, blurred vision, and nausea. Valproic acid (choice A) is an anticonvulsant, not associated with cinchonism. Isoniazid (choice C) is an antibiotic used to treat tuberculosis and does not cause cinchonism. Ethosuximide (choice D) is an anticonvulsant used to treat absence seizures and is not linked to cinchonism.

Correct Answer: A

Rationale: The correct answer is A: Hypertension is not a side effect of Sympathoplegics (Clonidine). Sympathoplegics are medications that inhibit the sympathetic nervous system, leading to decreased heart rate and blood pressure. Therefore, hypertension is not a common side effect. Choices B, C, and D are incorrect because difficulty breathing, dry oral cavity, and lethargic behavior are potential side effects of Sympathoplegics due to their central nervous system depressant effects.

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: Rationale: Lansoprazole is a proton pump inhibitor used to treat conditions related to excess stomach acid. Thalamus hypertrophy is not a condition affecting stomach acid production, making it unrelated to Lansoprazole use. A: Gastritis, B: Peptic Ulcers, and C: Zollinger-Ellison syndrome all involve excessive stomach acid secretion, hence Lansoprazole is used in these cases. Thalamus hypertrophy does not involve stomach acid issues, making it the correct answer.