Karinoya Learning Room

Qualifications · OTC Drug Seller (Tohan) Success Lab

Neuropsychiatric and Respiratory Medicines

Read the questions and explanations in English. The lectures (explanatory articles) are available in Japanese only.

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Q1 | Basics of the common cold

Which of the following statements about the common cold and cold remedies is correct?

  1. When accompanied by a sudden fever, or when symptoms continue for 4 days or more, the likelihood of it being a common cold is considered high.
  2. Because influenza (epidemic influenza) is, like the common cold, caused by respiratory infection with a virus, it is treated without distinction from the common cold.
  3. A cold remedy is a medicine that has the action of suppressing the proliferation of a virus or removing it from the body.
  4. About 80% of colds are caused by viral infection, but some are also caused by bacterial infection or, rarely, by a non-infectious factor such as cold air, dryness, or allergy.
AnswerD. About 80% of colds are caused by viral infection, but some are also caused by bacterial infection or, rarely, by a non-infectious factor such as cold air, dryness, or allergy.

The Guide states that about 80% of colds are caused by viral infection, but some are also caused by bacterial infection or, rarely, by a non-infectious factor such as cold air, dryness, or allergy. A cold remedy does not suppress or remove the virus; it is a symptomatic treatment intended to relieve the various symptoms. Because influenza is highly contagious and prone to becoming severe, it is treated distinctly from the common cold. When accompanied by a sudden fever, or when symptoms continue for 4 days or more, or when symptoms are severe, the likelihood of it 'not' being a common cold is considered high.

Q2 | Cold remedy ingredients

Which of the following statements about ingredients formulated in cold remedies and their classification is incorrect?

  1. Belladonna total alkaloids are formulated for the purpose of suppressing nasal secretion and sneezing through an anticholinergic action.
  2. Methylephedrine hydrochloride is an antihistamine ingredient formulated for the purpose of suppressing sneezing and runny nose.
  3. Tranexamic acid is an anti-inflammatory ingredient that suppresses the production of inflammation-causing substances in the body, thereby suppressing the occurrence of inflammation and relieving swelling.
  4. Guaifenesin is an expectorant ingredient formulated for the purpose of loosening phlegm.
AnswerB. Methylephedrine hydrochloride is an antihistamine ingredient formulated for the purpose of suppressing sneezing and runny nose.

Methylephedrine hydrochloride is an adrenergic ingredient formulated to relieve congestion of the nasal mucosa and dilate the trachea and bronchi, and is not an antihistamine ingredient. Antihistamine ingredients include chlorpheniramine maleate, carbinoxamine maleate, and mequitazine, among others. The action of tranexamic acid, guaifenesin being an expectorant ingredient, and belladonna total alkaloids suppressing nasal secretion and sneezing through anticholinergic action, all match the Guide's description.

Q3 | Glycyrrhizin

Which of the following statements about dipotassium glycyrrhizinate formulated in cold remedies is correct?

  1. For medicines, the dosage is set so that daily intake as glycyrrhizic acid does not exceed 40 mg.
  2. Regardless of who the intended user is, a product whose maximum daily dose amounts to 40 mg or more as glycyrrhizic acid should avoid long-term continued use.
  3. Taking a large amount of glycyrrhizic acid risks causing aseptic meningitis.
  4. Glycyrrhizic acid, the active component of dipotassium glycyrrhizinate, has a chemical structure resembling that of a vitamin-like substance.
AnswerB. Regardless of who the intended user is, a product whose maximum daily dose amounts to 40 mg or more as glycyrrhizic acid should avoid long-term continued use.

The Guide states that regardless of who the intended user is, a product whose maximum daily dose amounts to 40 mg or more as glycyrrhizic acid should avoid long-term continued use. It is a steroidal anti-inflammatory ingredient whose chemical structure resembles that of glycyrrhizic acid. For medicines, the dosage is set so that daily intake as glycyrrhizic acid does not exceed 200 mg. What can result from a large intake is pseudoaldosteronism; aseptic meningitis is a side effect that can occur with ibuprofen.

Q4 | Kampo for colds

Which of the following statements about kampo (Chinese herbal) formula products used to relieve cold symptoms is incorrect?

  1. In addition to maoto (麻黄湯), both kakkonto and shoseiryuto (小青竜湯) contain ephedra herb (麻黄, mao) among their constituent crude drugs.
  2. Hangekobokuto (半夏厚朴湯) contains glycyrrhiza (甘草, kanzo) among its constituent crude drugs.
  3. Keishito (桂栃湯) is said to be suited to the early stage of a cold, with sweating, in a person of weak constitution.
  4. Kakkonto (葛根湯) is said to be suited to the early stage of a cold (without sweating) in a person of medium build or above, as well as to a head cold, rhinitis, and headache.
AnswerB. Hangekobokuto (半夏厚朴湯) contains glycyrrhiza (甘草, kanzo) among its constituent crude drugs.

The Guide states that, of the nine kampo formula ingredients listed for cold remedies, all 'except' hangekobokuto contain glycyrrhiza as a constituent crude drug, meaning hangekobokuto does not contain glycyrrhiza. The description of the intended constitution (sho) for kakkonto and keishito, and the fact that ephedra herb is contained in maoto as well as kakkonto and shoseiryuto, both match the Guide's description.

Q5 | Shosaikoto

Which of the following statements about shosaikoto (小柴胡湯) is correct?

  1. Shosaikoto is stated to be particularly suited to a person of weak constitution (a person whose physical strength has declined, or a person of weak build), and unsuited to a person of robust constitution.
  2. For a person undergoing treatment with an interferon preparation, shosaikoto is stated to need its use avoided, since the risk of the side effect of interstitial pneumonia is heightened.
  3. Congestive heart failure and ventricular tachycardia are known as serious side effects of shosaikoto, and interstitial pneumonia or liver dysfunction is never seen, even rarely.
  4. Shosaikoto, like maoto, kakkonto, and shoseiryuto, is a kampo formula product containing ephedra herb (麻黄, mao) among its constituent crude drugs.
AnswerB. For a person undergoing treatment with an interferon preparation, shosaikoto is stated to need its use avoided, since the risk of the side effect of interstitial pneumonia is heightened.

The Guide states that for a person undergoing treatment with an interferon preparation, shosaikoto needs its use avoided, since the risk of the side effect of interstitial pneumonia is heightened, and that a person diagnosed with liver disease needs to consult before use. Ephedra herb is contained in maoto, kakkonto, and shoseiryuto. Shosaikoto is stated to be 'unsuited' to a person of weak constitution. Congestive heart failure and ventricular tachycardia are known with shakuyakukanzoto, and the serious side effects that can rarely occur with shosaikoto are interstitial pneumonia and liver dysfunction.

Q6 | Mechanism of antipyresis

Which of the following statements about the action of analgesic/antipyretic ingredients is incorrect?

  1. Suppressing the production of prostaglandin at the periphery increases renal blood flow, so it carries no risk of worsening symptoms even where kidney function is impaired.
  2. When prostaglandin's action of regulating gastric acid secretion and protecting the gastric mucosa is interfered with, gastric acid secretion increases while blood flow to the stomach wall decreases, making gastric mucosal damage more likely.
  3. Prostaglandin acts to keep body temperature regulated at a higher level than normal, and is also involved in the occurrence of inflammation.
  4. As for antipyresis, an action that promotes reabsorption of water in the kidney, increasing circulating blood volume, and promotes sweating, also contributes.
AnswerA. Suppressing the production of prostaglandin at the periphery increases renal blood flow, so it carries no risk of worsening symptoms even where kidney function is impaired.

The Guide states that suppressing the production of prostaglandin at the periphery 'decreases' renal blood flow, so it can worsen symptoms where kidney function is impaired. That prostaglandin regulates body temperature to be kept higher and is also involved in inflammation, that promoted reabsorption of water in the kidney increasing circulating blood volume and promoted sweating contribute to antipyresis, and that gastric mucosal damage becomes more likely, all match the Guide's description.

Q7 | Aspirin

Which of the following statements about salicylate analgesic/antipyretic ingredients is correct?

  1. Even in an OTC drug, aspirin (including aspirin aluminum) can be used by a child under 15 years of age if the dose is reduced.
  2. Ethenzamide and salicylamide need to have their use avoided in a child under 15 years of age who has chickenpox (varicella) or influenza.
  3. Aspirin is an ingredient said to cause gastrointestinal problems less readily compared with other analgesic/antipyretic ingredients.
  4. Aspirin needs to have its use avoided in a pregnant woman within 4 weeks of her expected delivery date.
AnswerB. Ethenzamide and salicylamide need to have their use avoided in a child under 15 years of age who has chickenpox (varicella) or influenza.

The Guide states that ethenzamide and salicylamide need to have their use avoided in a child under 15 years of age who has chickenpox (varicella) or influenza. Aspirin causes gastrointestinal problems 'more' readily compared with other analgesic/antipyretic ingredients. Aspirin (including aspirin aluminum), sazapyrine, and sodium salicylate must never be used as an OTC drug in a child under 15 years of age under any circumstances, given the suggested occurrence of Reye's syndrome. What aspirin needs avoided is use within '12 weeks' of the expected delivery date.

Q8 | Acetaminophen

Which of the following statements about acetaminophen is correct?

  1. It is used only as an oral medicine, and no product is used as a suppository.
  2. Because it produces antipyresis and analgesia mainly through a central action, no anti-inflammatory action at the periphery can be expected.
  3. Because it causes gastrointestinal problems more readily than other analgesic/antipyretic ingredients, it may never be taken on an empty stomach under any circumstances.
  4. In OTC drugs, it must never be used under any circumstances in a child under 15 years of age.
AnswerB. Because it produces antipyresis and analgesia mainly through a central action, no anti-inflammatory action at the periphery can be expected.

The Guide states that because acetaminophen produces antipyresis and analgesia mainly through a central action, no anti-inflammatory action at the periphery can be expected. Accordingly, it causes less gastrointestinal problems than other analgesic/antipyretic ingredients, and some products can be taken on an empty stomach, though taking it after a meal is recommended. What must never be used under any circumstances in a child under 15 years of age are ingredients such as aspirin and ibuprofen. There are also suppositories containing acetaminophen formulated as products used exclusively for reducing fever in children.

Q9 | Ibuprofen

Which of the following statements about ibuprofen is incorrect?

  1. In OTC drugs, given the suggested occurrence of Reye's syndrome, it must never be used under any circumstances in a child under 15 years of age.
  2. In a person with a history of a disease causing widespread inflammation of the digestive tract, such as a gastric or duodenal ulcer, ulcerative colitis, or Crohn's disease, it risks worsening symptoms or triggering a recurrence of that disease.
  3. It can rarely cause the serious side effect of aseptic meningitis, but is said to occur less readily, if anything, in a person with systemic lupus erythematosus or mixed connective tissue disease.
  4. It is not to be taken by a pregnant woman within 12 weeks of her expected delivery date.
AnswerC. It can rarely cause the serious side effect of aseptic meningitis, but is said to occur less readily, if anything, in a person with systemic lupus erythematosus or mixed connective tissue disease.

The Guide states that ibuprofen causes aseptic meningitis 'more readily' in a person with systemic lupus erythematosus or mixed connective tissue disease, so a response such as consulting a doctor or pharmacist about its suitability before use is necessary. That it must never be used under any circumstances in a child under 15 years of age, that it risks triggering a recurrence in a person with a history of a disease causing widespread inflammation of the digestive tract, and that it is not to be taken by a pregnant woman within 12 weeks of her expected delivery date, all match the Guide's description.

Q10 | Recommending a doctor's visit

Which of the following statements about recommending a doctor's visit and the like for cold remedies and analgesic/antipyretics is correct?

  1. For an infant under 2 years of age, a cold remedy is stated to be given before having them seen by a doctor.
  2. Ordinarily, if body temperature is 38°C or below, there is no risk of convulsions or marked exhaustion, so there is stated to be no need to use an analgesic/antipyretic until the temperature returns to normal.
  3. Even when a fever has continued for a week or more, there is no need to consider the possibility that an infection other than a cold, or some other serious illness, is the cause.
  4. It is stated to be preferable to use an analgesic/antipyretic preventively, before symptoms appear.
AnswerB. Ordinarily, if body temperature is 38°C or below, there is no risk of convulsions or marked exhaustion, so there is stated to be no need to use an analgesic/antipyretic until the temperature returns to normal.

The Guide states that ordinarily, if body temperature is 38°C or below, there is no risk of convulsions or marked exhaustion, so there is no need to use an analgesic/antipyretic until the temperature returns to normal. An analgesic/antipyretic is effective when taken while symptoms are mild, but using it preventively before symptoms appear is not appropriate. When a fever has continued for a week or more, an infection other than a cold, or some other serious illness, may be the cause. For an infant under 2 years of age, priority is given to having them seen by a doctor, with a cold remedy given only when this is unavoidable.

Q11 | Sleep-aid medicines

Which of the following statements about the antihistamine ingredient formulated in a drowsiness-inducing medicine (a hypnotic sedative) is incorrect?

  1. Sleep disturbance that often occurs during pregnancy is not a use for which a sleep-aid medicine is intended.
  2. A hypnotic sedative with an antihistamine ingredient as its main ingredient is intended for use by a person who has been diagnosed with insomnia at a medical institution.
  3. Histamine plays a role in maintaining and regulating wakefulness, via stimulation of nerve cells at a site involved in sleep and wakefulness in the lower part of the brain.
  4. Diphenhydramine hydrochloride, among antihistamine ingredients, has a particularly strong central action.
AnswerB. A hypnotic sedative with an antihistamine ingredient as its main ingredient is intended for use by a person who has been diagnosed with insomnia at a medical institution.

The Guide states that a hypnotic sedative with an antihistamine ingredient as its main ingredient, as a sleep-aid medicine, is used to relieve temporary sleep disturbance (difficulty falling asleep, light sleep), and is not intended for a person with chronic insomnia symptoms, or a person who has been diagnosed with insomnia at a medical institution. That histamine plays a role in maintaining and regulating wakefulness, that diphenhydramine hydrochloride has a particularly strong central action, and that sleep disturbance during pregnancy is not an intended use, all match the Guide's description.

Q12 | Sedative ingredients

Which of the following statements about precautions for use of hypnotic sedatives is correct?

  1. Allylisopropylacetylurea has an action that heightens excitement of the brain and sharpens pain sensation, so its use should be kept to a small amount.
  2. In children and young people, an antihistamine ingredient can cause nervous excitability or central excitement, the opposite of drowsiness; in particular, use of a sleep-aid medicine containing an antihistamine ingredient should be avoided in a child under 15 years of age.
  3. Bromovalerylurea has an action that suppresses excitement of the brain, but is an ingredient that never causes dependence even with repeated intake.
  4. Because an effect on the fetus has been ruled out for bromovalerylurea, there is no need for a pregnant woman, or a woman thought to be pregnant, to avoid using it as a hypnotic sedative.
AnswerB. In children and young people, an antihistamine ingredient can cause nervous excitability or central excitement, the opposite of drowsiness; in particular, use of a sleep-aid medicine containing an antihistamine ingredient should be avoided in a child under 15 years of age.

The Guide states that in children and young people, an antihistamine ingredient can cause nervous excitability or central excitement, the opposite of drowsiness, and that because such side effects occur particularly readily in a child under 15 years of age, use of a sleep-aid medicine should be avoided in such children. Both bromovalerylurea and allylisopropylacetylurea have an action that 'suppresses' excitement of the brain and 'dulls' pain sensation, and are known to cause dependence with repeated intake. Bromovalerylurea can potentially cause a disorder in the fetus, so a pregnant woman and the like should avoid using it.

Q13 | Sedative crude drugs

Which of the following statements about a crude drug ingredient formulated in a hypnotic sedative for its sedative action is incorrect?

  1. Uncaria hook (釣藤鉤, chotoko) is a crude drug derived from the typically thorny part of Uncaria species and the like, of the family Rubiaceae.
  2. Jujube seed (酸棵仁, sansonin) is a crude drug derived from the seed of Ziziphus jujuba var. spinosa, of the family Rhamnaceae.
  3. Valerian root (カノコソウ, kanokoso) is also known as 'passiflora', a plant of the family Passifloraceae native to South America.
  4. Even a sedative consisting solely of crude drug ingredients should avoid combining multiple sedatives or long-term continued use.
AnswerC. Valerian root (カノコソウ, kanokoso) is also known as 'passiflora', a plant of the family Passifloraceae native to South America.

The Guide states that kanokoso is also known as 'kissokon', a crude drug derived from the root and rhizome of Valeriana fauriei, of the family Valerianaceae. It is chabotokeiso (Passiflora incarnata) that is also known as passiflora, a plant of the family Passifloraceae native to South America. The origins of chotoko and sansonin, and the fact that even a sedative consisting solely of crude drug ingredients should avoid combination use or long-term continued use, both match the Guide's description.

Q14 | Kampo for insomnia

Which of the following statements about kampo formula products intended to improve symptoms such as nervousness, mental unrest, and insomnia is correct?

  1. For sansoninto (酸棵仁湯), if no improvement in symptoms is seen after about a week of use, it is stated that continuing use indefinitely should be avoided and a response such as visiting a medical institution is needed.
  2. Saikokaryukotsuboreito (柴胡加竜骨牡蠣湯) contains glycyrrhiza (甘草, kanzo) among its constituent crude drugs.
  3. Keishikaryukotsuboreito (桂栃加竜骨牡蠣湯) is said to be suited to a person of medium build or above with mental unrest, accompanied by palpitations, insomnia, and constipation.
  4. Yokukansan (抑胆散) is stated to carry no possibility of causing heart failure.
AnswerA. For sansoninto (酸棵仁湯), if no improvement in symptoms is seen after about a week of use, it is stated that continuing use indefinitely should be avoided and a response such as visiting a medical institution is needed.

The Guide states that for sansoninto, if no improvement in symptoms is seen after about a week of use, continuing use indefinitely should be avoided and a response such as visiting a medical institution is needed. Among the kampo formula products in this section, all 'except' saikokaryukotsuboreito contain glycyrrhiza, and saikokaryukotsuboreito instead contains rhubarb root (大黄, daio). Yokukansan is stated to carry a possibility of causing heart failure. The one said to be suited to a person of medium build or above with palpitations, insomnia, and constipation is saikokaryukotsuboreito, while keishikaryukotsuboreito is said to be suited to a person of medium build or below who tires easily, is nervous, and is prone to excitement.

Q15 | Action of caffeine

Which of the following statements about the action of caffeine formulated in an anti-drowsiness medicine is incorrect?

  1. Caffeine has an action that suppresses the heart muscle, and can cause bradycardia as a side effect.
  2. Caffeine has an action that suppresses reabsorption of sodium ions (and, along with them, water) in the kidney, bringing about an increase in urine volume (diuresis).
  3. Caffeine has an action that increases gastric juice secretion, and can cause gastrointestinal problems such as loss of appetite and nausea/vomiting as side effects.
  4. Caffeine has the property, though its action is weak, of forming dependence with repeated intake.
AnswerA. Caffeine has an action that suppresses the heart muscle, and can cause bradycardia as a side effect.

The Guide states that caffeine has an action that 'stimulates' the heart muscle, and can cause palpitations as a side effect, so a person with heart disease should avoid taking it. Its diuretic action from suppressing reabsorption of sodium ions, its gastrointestinal problems from an action that increases gastric juice secretion (for which reason a person with excess stomach acid or a gastric ulcer should avoid taking it), and its property of forming dependence with repeated intake, all match the Guide's description.

Q16 | Caffeine amount

Which of the following statements about caffeine intake and the like in anti-drowsiness medicines is correct?

  1. For caffeine in an anti-drowsiness medicine, the upper limit is 200 mg as caffeine per single intake, and 500 mg as caffeine per day.
  2. For caffeine in an anti-drowsiness medicine, the upper limit for daily intake is 200 mg as caffeine.
  3. Because caffeine taken in does not transfer into breast milk, there is no need to consider the effect on the infant even if a breastfeeding woman takes a large amount.
  4. Although caffeine has an action that increases gastric juice secretion, there is no need for a person with excess stomach acid or a gastric ulcer to avoid taking an anti-drowsiness medicine.
AnswerA. For caffeine in an anti-drowsiness medicine, the upper limit is 200 mg as caffeine per single intake, and 500 mg as caffeine per day.

The Guide states that for caffeine in an anti-drowsiness medicine, the upper limit is 200 mg as caffeine per single intake, and 500 mg as caffeine per day. Because it has an action that increases gastric juice secretion, a person with excess stomach acid or a gastric ulcer should avoid taking it. Part of the caffeine taken in transfers into breast milk, and because an infant's liver is undeveloped and takes more time to metabolize it, care should be taken during breastfeeding not to let the total intake become continuously large.

Q17 | Anti-drowsiness medicine

Which of the following statements about the use of anti-drowsiness medicine is incorrect?

  1. Because drowsiness occurring during infection with a bacterium, virus, or the like has no relation to the body's defenses, there is no problem in suppressing it with an anti-drowsiness medicine.
  2. Even after getting sufficient sleep, if drowsiness or malaise continues that use of an anti-drowsiness medicine cannot suppress, a response such as visiting a medical institution is necessary.
  3. It is not appropriate to use an anti-drowsiness medicine to suppress drowsiness caused by using a cold remedy, antiallergic drug, or the like.
  4. Because sleep is important for the development of a growing child, there is no anti-drowsiness medicine for children, and care must be taken to ensure it is never used in a child under 15 years of age.
AnswerA. Because drowsiness occurring during infection with a bacterium, virus, or the like has no relation to the body's defenses, there is no problem in suppressing it with an anti-drowsiness medicine.

The Guide states that drowsiness occurring during infection with a bacterium, virus, or the like, like fever, is a pathophysiological response that plays an important part in the body's defenses, and that interfering with sleep at such a time using an anti-drowsiness medicine risks delaying recovery from the illness. That there is no anti-drowsiness medicine for children and care must be taken to ensure it is never used in a child under 15 years of age, that using it for the purpose of suppressing drowsiness caused by another medicine is not appropriate, and the recommendation to visit a doctor when drowsiness or malaise that cannot be suppressed continues, all match the Guide's description.

Q18 | Motion-sickness ingredients

Which of the following statements about ingredients formulated in motion-sickness prevention medicines is correct?

  1. Scopolamine hydrobromide hydrate is metabolized slowly in the liver, so its action lasts longer compared with other antihistamine ingredients.
  2. Meclizine hydrochloride is an antihistamine ingredient characterized by its action appearing faster and its duration being shorter compared with other antihistamine ingredients.
  3. Difenidol hydrochloride shows a regulating action on the nerve connecting the vestibule in the inner ear to the brain (the vestibular nerve), as well as an action that improves blood flow to the inner ear.
  4. Dimenhydrinate is the generic name of an anticholinergic ingredient formulated exclusively in motion-sickness prevention medicines.
AnswerC. Difenidol hydrochloride shows a regulating action on the nerve connecting the vestibule in the inner ear to the brain (the vestibular nerve), as well as an action that improves blood flow to the inner ear.

The Guide states that difenidol hydrochloride shows a regulating action on the nerve connecting the vestibule in the inner ear to the brain (the vestibular nerve), as well as an action that improves blood flow to the inner ear. Dimenhydrinate is the generic name of diphenhydramine theoclate, an 'antihistamine' ingredient formulated exclusively in motion-sickness prevention medicines. Meclizine hydrochloride has its action appear 'more slowly' and last 'longer'. Because scopolamine hydrobromide hydrate is metabolized quickly in the liver, its action lasts 'shorter' compared with antihistamine ingredients and the like.

Q19 | Cautions for anti-motion-sickness medicine

Which of the following statements about precautions for use of motion-sickness prevention medicines is incorrect?

  1. For ingredients containing promethazine, such as promethazine hydrochloride, because fatal respiratory depression has been reported overseas, use needs to be avoided in a child under 15 years of age.
  2. When ethyl aminobenzoate is formulated, use needs to be avoided in a child under 6 years of age.
  3. Because a motion-sickness prevention medicine also contains an ingredient mainly intended to suppress nausea, using it to cope with the nausea of morning sickness is appropriate.
  4. Motion sickness is said to hardly ever occur in a child under 3 years of age, and there is no motion-sickness prevention medicine product intended for an infant under 3 years of age.
AnswerC. Because a motion-sickness prevention medicine also contains an ingredient mainly intended to suppress nausea, using it to cope with the nausea of morning sickness is appropriate.

The Guide states that although a motion-sickness prevention medicine also contains an ingredient mainly intended to suppress nausea, using it to cope with the nausea of morning sickness is 'not appropriate'. That use of a promethazine-containing ingredient needs to be avoided in a child under 15 years of age, given reports of sudden infant death syndrome and the like, that use of ethyl aminobenzoate needs to be avoided in a child under 6 years of age, and that motion sickness hardly ever occurs in a child under 3 years of age with no product intended for that age, all match the Guide's description.

Q20 | Children's night-crying/fretfulness

Which of the following statements about crude drug preparations and kampo formula products indicated for a child's 'kan' (fretfulness/night-crying) is correct?

  1. Antelope horn (レイヨウカク, reiyokaku) is a crude drug derived from the horn of the saiga antelope and the like, of the family Bovidae, used for its expected action of calming tension and excitement.
  2. Agarwood (沈香, jinko) is a crude drug derived from the wood of Aquilaria and the like, of the family Thymelaeaceae, used for its expected laxative action.
  3. A sedative for children is recommended to be used with priority given to securing the guardian's own restful sleep and the like.
  4. A kampo formula product may be used even in an infant under 3 months of age, as long as no lower age limit is set in its dosage and administration.
AnswerA. Antelope horn (レイヨウカク, reiyokaku) is a crude drug derived from the horn of the saiga antelope and the like, of the family Bovidae, used for its expected action of calming tension and excitement.

The Guide states that reiyokaku is a crude drug derived from the horn of the saiga antelope and the like, of the family Bovidae, used for its expected action of calming tension and excitement. Jinko is used for its expected sedative, stomachic, and tonic actions, among others. A kampo formula product is not to be used in an infant under 3 months of age, even where no lower age limit is set in its dosage and administration. Using a sedative for children with priority given to securing the guardian's own restful sleep and the like is stated to be not appropriate.

Q21 | Antitussive ingredients

Which of the following statements about antitussive ingredients formulated in antitussive/expectorant medicines is incorrect?

  1. Dextromethorphan hydrobromide hydrate is classified as a narcotic antitussive ingredient.
  2. Pinellia tuber (半夏, hange) is a crude drug derived from the tuber, with the cork layer removed, of Pinellia ternata of the family Araceae, and shows a central antitussive action.
  3. Codeine phosphate hydrate and dihydrocodeine phosphate are also called narcotic antitussive ingredients.
  4. A cough is a response triggered when some abnormality occurs in the trachea or bronchi, the stimulus is conveyed to the central nervous system, and the cough center in the medulla oblongata acts.
AnswerA. Dextromethorphan hydrobromide hydrate is classified as a narcotic antitussive ingredient.

The Guide states that dextromethorphan hydrobromide hydrate, along with noscapine and tipepidine hibenzate, is also called a 'non-narcotic antitussive ingredient'. It is codeine phosphate hydrate and dihydrocodeine phosphate, whose active component shares the same basic structure as morphine, that are called narcotic antitussive ingredients. That the cough center is in the medulla oblongata, and the origin and central antitussive action of pinellia tuber, both match the Guide's description.

Q22 | Codeine-type ingredients

Which of the following statements about codeine phosphate hydrate and dihydrocodeine phosphate is correct?

  1. They show an action that increases motility of the digestive tract, and diarrhea can appear as a side effect.
  2. Even if taken during pregnancy, none of the absorbed component crosses the blood-placenta barrier and transfers to the fetus.
  3. Because they never transfer into breast milk, they may be taken without any problem even by a person breastfeeding.
  4. From the standpoint of reducing the risk of respiratory depression in children, it was decided, in principle, that a caution be issued so that medicines containing these are not used in a child under 12 years of age and the like.
AnswerD. From the standpoint of reducing the risk of respiratory depression in children, it was decided, in principle, that a caution be issued so that medicines containing these are not used in a child under 12 years of age and the like.

The Guide states that, from the standpoint of reducing as far as possible the risk of respiratory depression in children caused by codeine-type ingredients, precautionary measures were taken, including, in principle, issuing a caution so that this medicine is not used in a child under 12 years of age and the like. Codeine-type ingredients show an action that 'decreases' motility of the digestive tract, and constipation can appear as a side effect. When taken during pregnancy, part of the absorbed component is known to cross the blood-placenta barrier and transfer to the fetus. There are reports of morphine intoxication occurring in infants due to transfer into breast milk, so a person breastfeeding needs to either not take it or avoid breastfeeding during use.

Q23 | Bronchodilation

Which of the following statements about bronchodilator ingredients formulated in antitussive/expectorant medicines is incorrect?

  1. Xanthine-derivative ingredients such as diprophylline dilate the bronchi by relaxing the smooth muscle of the bronchi via the autonomic nervous system.
  2. Adrenergic ingredients such as methylephedrine hydrochloride show an action that stimulates the sympathetic nervous system to dilate the bronchi.
  3. For adrenergic ingredients and ephedra herb, a person diagnosed with heart disease, high blood pressure, diabetes, or hyperthyroidism should consult a doctor or pharmacist about their suitability before use.
  4. Ephedra herb (麻黄, mao) is a crude drug derived from the above-ground stem of a plant of the family Ephedraceae, and is also expected to have actions such as promoting sweating and diuresis, in addition to bronchodilation.
AnswerA. Xanthine-derivative ingredients such as diprophylline dilate the bronchi by relaxing the smooth muscle of the bronchi via the autonomic nervous system.

The Guide states that xanthine-derivative ingredients such as diprophylline are ingredients that dilate the bronchi by acting directly on the smooth muscle of the bronchi to relax it, 'without going via the autonomic nervous system'. Note that a person diagnosed with a thyroid function disorder or epilepsy needs to consult before using a xanthine-derivative ingredient. That an adrenergic ingredient stimulates the sympathetic nervous system to dilate the bronchi, the origin and action of ephedra herb, and the need to consult for a person with an underlying disease such as heart disease, all match the Guide's description.

Q24 | Expectorant ingredients

Which of the following statements about expectorant ingredients formulated in antitussive/expectorant medicines is correct?

  1. Guaifenesin shows an action that dissolves and reduces the molecular size of viscous protein in phlegm, decreasing its viscosity.
  2. Carbocisteine shows an action that adjusts the proportion of mucus components, improving the ease of expelling phlegm.
  3. Bromhexine hydrochloride shows only an action that suppresses secretion of mucus from the airway mucosa.
  4. Ethyl cysteine hydrochloride improves the ease of expelling phlegm by suppressing ciliary movement of the airway mucosa.
AnswerB. Carbocisteine shows an action that adjusts the proportion of mucus components, improving the ease of expelling phlegm.

The Guide lists carbocisteine as adjusting the proportion of mucus components and improving the ease of expelling phlegm (it also shows an action of dissolving and reducing the molecular size of viscous protein in phlegm). Guaifenesin shows an action that 'promotes secretion' of mucus from the airway mucosa. Bromhexine hydrochloride shows an action that promotes secretion, an action that dissolves and reduces molecular size, and an action that promotes ciliary movement. Ethyl cysteine hydrochloride is one that dissolves and reduces the molecular size of viscous protein in phlegm, decreasing its viscosity.

Q25 | Glycyrrhiza

Which of the following statements about glycyrrhiza (甘草, kanzo) used in antitussive/expectorant medicines is correct?

  1. Glycyrrhiza is a crude drug used only in medicines, and is never used as a sweetener in ordinary foods, so there is no need to draw attention to the total amount of glycyrrhizic acid either.
  2. Glycyrrhiza is a crude drug derived from the root and stolon of a plant of the family Fabaceae, and in addition to the anti-inflammatory action of glycyrrhizic acid, is also expected to have actions such as promoting mucus secretion from the airway mucosa.
  3. A product whose maximum daily dose amounts to 10 g or more as glycyrrhiza (converted to crude drug equivalent) should avoid long-term continued use, since it risks causing pseudoaldosteronism.
  4. Kanzoto (甘草湯) is a kampo formula product consisting of two constituent crude drugs, glycyrrhiza and ephedra herb.
AnswerB. Glycyrrhiza is a crude drug derived from the root and stolon of a plant of the family Fabaceae, and in addition to the anti-inflammatory action of glycyrrhizic acid, is also expected to have actions such as promoting mucus secretion from the airway mucosa.

The Guide states that glycyrrhiza is a crude drug derived from the root and stolon (with the periderm sometimes removed) of a plant of the family Fabaceae, and in addition to the anti-inflammatory action of glycyrrhizic acid, is also expected to have actions such as promoting mucus secretion from the airway mucosa. What should avoid long-term continued use is a product whose maximum daily dose amounts to '1 g' or more as glycyrrhiza (converted to crude drug equivalent). Kanzoto is a kampo formula product whose constituent crude drug is glycyrrhiza 'alone'. Because glycyrrhiza is also widely used as a sweetener in ordinary foods, drawing attention to the total amount of glycyrrhizic acid is stated to be important.

Q26 | Antitussive/expectorant crude drugs

Which of the following statements about crude drug ingredients formulated in antitussive/expectorant medicines is incorrect?

  1. Ophiopogon tuber (麦門冬, bakumondo) is a crude drug derived from the enlarged part of the root of Ophiopogon japonicus, of the family Liliaceae, used for its expected antitussive, expectorant, and tonic actions.
  2. Nandina fruit (南天実, nantenjitsu) is a crude drug derived from the whole flowering plant of Plantago asiatica, of the family Plantaginaceae, used for its expected expectorant action.
  3. Sekisan (石蒜) is a crude drug derived from the bulb of Lycoris radiata, of the family Amaryllidaceae, used for its expected expectorant action.
  4. Apricot kernel (杏仁, kyonin) is a crude drug derived from the seed of Prunus armeniaca var. ansu, Prunus armeniaca, and the like, of the family Rosaceae, and part of the metabolite produced from its breakdown in the body is said to show an action that sedates the respiratory center and cough center in the medulla oblongata.
AnswerB. Nandina fruit (南天実, nantenjitsu) is a crude drug derived from the whole flowering plant of Plantago asiatica, of the family Plantaginaceae, used for its expected expectorant action.

The Guide states that nandina fruit is a crude drug derived from the fruit of Nandina domestica f. leucocarpa (white-fruited nandina) or Nandina domestica, of the family Berberidaceae, said to act on sensory nerves and peripheral motor nerves to be effective against coughing. It is plantain herb (車前草, shazenso) that is derived from the whole flowering plant of Plantago asiatica, of the family Plantaginaceae, used for its expected expectorant action. The origins and actions of apricot kernel, sekisan, and ophiopogon tuber all match the Guide's description.

Q27 | Senega and onji

Which of the following statements about senega and onji is correct?

  1. A caution regarding ingredients and their amount is noted for a product containing 10 g or more of senega, as crude drug, at its maximum daily formulated amount.
  2. Senega and onji are both crude drugs derived from a plant of the family Polygalaceae, used for their expected expectorant action.
  3. Onji is a crude drug derived from the root of a plant of the family Campanulaceae.
  4. Intake of these crude drug ingredients can affect blood pressure test values.
AnswerB. Senega and onji are both crude drugs derived from a plant of the family Polygalaceae, used for their expected expectorant action.

The Guide states that senega is a crude drug derived from the root of Polygala senega or Polygala senega var. latifolia, and onji from the root and root bark of Polygala tenuifolia, both of the family Polygalaceae, both used for their expected expectorant action. Intake of these affects 'diabetes' test values, risking a mistaken impression that diabetes has improved. A caution is noted for a product containing '1.2 g' or more of senega, as crude drug, or 1 g or more as onji, at its maximum daily formulated amount. The crude drug derived from the root of a plant of the family Campanulaceae is platycodon root (桔梗, kikyo).

Q28 | Recommending a doctor's visit for coughs

Which of the following statements about recommending a doctor's visit and the like for antitussive/expectorant medicines is incorrect?

  1. No antipyretic ingredient is formulated in antitussive/expectorant medicines, so an effect of bringing down a fever cannot be expected.
  2. If symptoms such as coughing, phlegm, and breathlessness have continued for a long period, chronic obstructive pulmonary disease (COPD), such as chronic bronchitis or emphysema, may be a possibility.
  3. If asthma attacks recur repeatedly, it is preferable to continue using an OTC antitussive/expectorant medicine.
  4. A continuing dry cough without phlegm can potentially be an early symptom of interstitial pneumonia and the like.
AnswerC. If asthma attacks recur repeatedly, it is preferable to continue using an OTC antitussive/expectorant medicine.

The Guide states that with asthma, if inflammation of the bronchial mucosa has become chronic, even if an antitussive/expectorant medicine temporarily suppresses symptoms, an attack tends to recur again after a while, and status asthmaticus can lead to life-threatening difficulty breathing, so a response such as promptly seeking medical care rather than trying to cope with an OTC drug is necessary. That no antipyretic ingredient is formulated in antitussive/expectorant medicines, the possibility of interstitial pneumonia with a continuing dry cough, and the relationship between long-continuing cough/phlegm/breathlessness and COPD, all match the Guide's description.

Q29 | Gargle preparations

Which of the following statements about how to use oral/throat medicines and gargle preparations is correct?

  1. Because a gargle preparation is more effective the more concentrated the prepared liquid is, it is best used undiluted with water.
  2. A troche or lozenge has its active ingredient absorbed more quickly and its effect heightened by being chewed and swallowed, rather than sucked slowly in the mouth to dissolve.
  3. For a spray-type liquid preparation, it is preferable to spray while inhaling deeply, so that the liquid reaches all the way to the back of the pharynx.
  4. For a gargle preparation, it is stated to be effective to generally hold about 10 to 20 mL of the liquid in the mouth, tilt the face upward, gargle repeatedly so the liquid reaches all the way to the back of the pharynx, and then spit it out, repeating this several times.
AnswerD. For a gargle preparation, it is stated to be effective to generally hold about 10 to 20 mL of the liquid in the mouth, tilt the face upward, gargle repeatedly so the liquid reaches all the way to the back of the pharynx, and then spit it out, repeating this several times.

The Guide states that, as an effective way of gargling with a gargle preparation, it is effective to hold about 10 to 20 mL of the liquid in the mouth, tilt the face upward, gargle repeatedly so the liquid reaches all the way to the back of the pharynx, and then spit it out, repeating this several times. A troche or lozenge is important to dissolve slowly without chewing, and its effect cannot be expected if chewed and swallowed. A spray-type liquid preparation is preferably sprayed while exhaling lightly, since inhaling risks it entering the bronchi or lungs. A gargle preparation does not achieve sufficient effect if the prepared concentration is too strong or too weak.

Q30 | Germicidal/antiseptic ingredients

Which of the following statements about germicidal/antiseptic ingredients formulated in oral/throat medicines and gargle preparations is incorrect?

  1. A gargle preparation containing chlorhexidine gluconate is stated to be less irritating and easy to use, even for a person with a wound or severe sore in the oral cavity.
  2. With a gargle preparation containing povidone-iodine, its use can discolor a silver-containing dental material (such as dentures).
  3. Iodine loses its germicidal action, undergoing decolorization, when it reacts with a component such as vitamin C contained in lemon juice or tea.
  4. When an iodine-based germicidal/antiseptic ingredient is used in the oral cavity, it can result in intake of iodine, potentially affecting hormone production in the thyroid gland.
AnswerA. A gargle preparation containing chlorhexidine gluconate is stated to be less irritating and easy to use, even for a person with a wound or severe sore in the oral cavity.

The Guide states that a gargle preparation containing chlorhexidine gluconate needs to have its use avoided in a person with a wound or severe sore in the oral cavity, since it risks causing strong irritation. The effect of an iodine-based germicidal/antiseptic ingredient on thyroid hormone production (a person diagnosed with thyroid disease should consult), the discoloration of silver-containing dental materials by povidone-iodine, and the decolorization and loss of germicidal action from reaction with vitamin C, all match the Guide's description.

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