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1. One of the most frequently asked questions concerns mixedagonist-anatagonists (MAA) – they ask you to identify which drugs out of a list of 5 is an MAA. The one they usually expect you to know is pentazocine, but sometimes nalbuphine. Since these drugs have proved to be not very popular with patients, they have fallen out of use, so I would imagine that they don’t ask so many questions on these drugs anymore.
2. Additional drug identifications they always ask involve knowing that naloxone is an antagonist used to treat overdose, and that methadone is used in detoxification of morphine addicts.
3. Some questions give you a list of pharmacological effects and ask you to identify which is not an effect of morphine. Morphine produces respiratory depression, euphoria, sedation, dysphoria, analgesia, and constipation and urinary retention. The substitution they often make is diarrhea for constipation, or perhaps diuresis for urinary retention.
4. The last most frequently asked type of question regarding opiates concerns overdose of toxicity. In overdose morphine causes coma, miosis, and respiratory depression. Sometimes they ask the mechanism of respiratory depression: loss of sensitivity of the medullary respiratory center to carbon dioxide.
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Occurrence of which of the following is LEAST characteristic of narcotic ingestion?
(b) Again, the key word is least. Narcotics, in the form of paregoric (tincture of opium), and Lomotil (loperamide) are over the counter oral preparations for the treatment of diarrhea. Opiates act on receptors in the gut to produce constipation. Thus (b) is obviously wrong. All of the other answers are side effects of opiate administration.
(b) Again, the key word is least. Narcotics, in the form of paregoric (tincture of opium), and Lomotil (loperamide) are over the counter oral preparations for the treatment of diarrhea. Opiates act on receptors in the gut to produce constipation. Thus (b) is obviously wrong. All of the other answers are side effects of opiate administration.
Therapeutic doses of morphine administered intramuscularly may produce
a. Constipation
b. Euphoria
c. Dysphoria
d. Mental clouding
e. Decreased response to pain
(v) memorize
(v) memorize
Which of the following are pharmacologic effects of morphine?
a. Respiratory depression
b. Euphoria
c. Sedation
d. Constipation
e. Dysphoria
Which of the following drugs acts to suppress the cough reflex?
(b) the only drugs that do this are opioids, and codeine and merperidine are the two opioids on the list. Of the two, codeine is much better at this than meperidine.
(b) the only drugs that do this are opioids, and codeine and merperidine are the two opioids on the list. Of the two, codeine is much better at this than meperidine.
Morphine binds to which site to produce analgesia?
(a) They might reword the question in a way that asks you to remember that the specific receptors are the mu receptors.
(a) They might reword the question in a way that asks you to remember that the specific receptors are the mu receptors.
Morphine causes vomiting by
(c) So it seems they want you to think that the emetic response to morphine is locally activated, but actually it is an effect produced by morphine acting on the CTZ in the medulla.
(c) So it seems they want you to think that the emetic response to morphine is locally activated, but actually it is an effect produced by morphine acting on the CTZ in the medulla.
The decrease in ventilation caused by morphine, meperidine and some of the related opioids depends chiefly upon
(e) memorization. Don’t be fooled by (a)- these drugs are sedating, but this has nothing to do with the decrease in respiratory rate
(e) memorization. Don’t be fooled by (a)- these drugs are sedating, but this has nothing to do with the decrease in respiratory rate
Small doses of barbiturates and morphine depress respiration primarily by
Which of the following are pathognomonic symptoms of narcotic overdose?
(a) pinpoint pupils (miosis) and respiratory depression are hallmark opioid overdose effects, so the only distractor is coma or convulsions. If you can’t breathe too well, I guess you might go into a coma!
(a) pinpoint pupils (miosis) and respiratory depression are hallmark opioid overdose effects, so the only distractor is coma or convulsions. If you can’t breathe too well, I guess you might go into a coma!
The cause of death with opioid intoxication is
(e) – again, a memorization question. What happens is that opioids decrease the response of respiratory centers in the brainstem to the carbon dioxide tension of the blood, and also depresses pontine and medullary centers regulating respiratory frequency. Opioids do not cause oxygen apnea, ((a)), they can be convulsive, but not terminally so ((c)), they are stabilizing on the heart and some are actually used in open-heart surgery ((b)), and they do not cause circulatory collapse ((d)).
(e) – again, a memorization question. What happens is that opioids decrease the response of respiratory centers in the brainstem to the carbon dioxide tension of the blood, and also depresses pontine and medullary centers regulating respiratory frequency. Opioids do not cause oxygen apnea, ((a)), they can be convulsive, but not terminally so ((c)), they are stabilizing on the heart and some are actually used in open-heart surgery ((b)), and they do not cause circulatory collapse ((d)).
Which of the following is an opioid that has both agonistic and antagonistic activities?
(e) This is an example of the type of question where the drug class is given. You are asked to not only identify a drug from the list as being from this class, but additionally that it has the properties that are given in the question that distinguish it from the other drugs of the class that are listed as alternatives. In this example, there is only one drug which meets this criterion. All are drugs which act via opiate receptors, but 3 are agonists ((a), (b), (d)), 1 is an antagonist only ((c)). (e) pentazocine is the only drug which has both types of action, and is the one drug left by the process of elimination.
(e) This is an example of the type of question where the drug class is given. You are asked to not only identify a drug from the list as being from this class, but additionally that it has the properties that are given in the question that distinguish it from the other drugs of the class that are listed as alternatives. In this example, there is only one drug which meets this criterion. All are drugs which act via opiate receptors, but 3 are agonists ((a), (b), (d)), 1 is an antagonist only ((c)). (e) pentazocine is the only drug which has both types of action, and is the one drug left by the process of elimination.
A heroin-dependent patient should NOT be given nalbuphine (Nubain) for pain because
(c) see above
(c) see above
A patient while not currently taking drugs has a history (6 months ago) of narcotic dependency. Which of the following analgesics should be avoided in this patient?
(b) see above
(b) see above
Which of the following statements does NOT characterize pentazocine?
The antagonist of choice in the treatment of opioid overdosage is
(a) nalorphine and pentazocine are mixed agonist-antagonists, levallorphan is an opioid agonist, as is propoxyphene
(a) nalorphine and pentazocine are mixed agonist-antagonists, levallorphan is an opioid agonist, as is propoxyphene
Which of the following is a complete antagonist of the opioid receptor and the agent of choice in the treatment of narcotic overdose?
(a) reworded version of the preceding question
Methadone is used in detoxification (drug withdrawal) of patients physically dependent on morphine because methadone
(d) This is an example of the kind of question that requires that you have memorized a fact about a particular drug, in this case the fact is (d). Methadone you will remember is not an antagonist like naloxone- it is a full agonist with analgesic properties, just like morphine. When taken orally it is not euphoric in addicts, but acts just like morphine to produce tolerance and physical dependence. Withdrawal is less severe than with morphine because methadone has a much longer half life. Facts 1, 2, and 3 would be met by an antagonist such as naloxone, or perhaps even a mixed agonist-antagonist such as pentazocine.
(d) This is an example of the kind of question that requires that you have memorized a fact about a particular drug, in this case the fact is (d). Methadone you will remember is not an antagonist like naloxone- it is a full agonist with analgesic properties, just like morphine. When taken orally it is not euphoric in addicts, but acts just like morphine to produce tolerance and physical dependence. Withdrawal is less severe than with morphine because methadone has a much longer half life. Facts 1, 2, and 3 would be met by an antagonist such as naloxone, or perhaps even a mixed agonist-antagonist such as pentazocine.
Which of the following drugs is currently widely used in treating opioid-dependent individuals?
(b) shortened version of the above question
(b) shortened version of the above question
Meperidine (Demerol) is