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配伍选择题 (2023年真题)1,4-二氢吡啶类钙通道阻滞药的母核结构是( )
A A.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442787_0.png"> B B.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442787_0_1.png"> C C.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442787_0_2.png"> D D.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442787_0_3.png"> E E.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442787_0_4.png">
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配伍选择题 (2023年真题)苯二氮卓类镇静催眠药的母核结构是( )
A A.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442788_0.png"> B B.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442788_0_1.png"> C C.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442788_0_2.png"> D D.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442788_0_3.png"> E E.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442788_0_4.png">
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配伍选择题 (2023年真题)磺酰脲类降糖药的母核结构是 ( )
A A.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442789_0.png"> B B.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442789_0_1.png"> C C.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442789_0_2.png"> D D.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442789_0_3.png"> E E.<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442789_0_4.png">
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配伍选择题 (2023年真题)微粒制剂是药物或与适宜载体,经过一定的分散包埋技术制得具有一定粒径(微米级或纳米级)的微粒组成的固态、液态或气态药物制剂。处方中含
A 纳米乳 B 脂质体 C 纳米粒 D 微囊 E 微球
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配伍选择题 (2023年真题)微粒制剂是药物或与适宜载体,经过一定的分散包埋技术制得具有一定粒径(微米级或纳米级)的微粒组成的固态、液态或气态药物制剂。采用白蛋
A 纳米乳 B 脂质体 C 纳米粒 D 微囊 E 微球
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配伍选择题 (2023年真题)药物在尚未吸收进入体循环之前,在肠黏膜和肝脏被代谢而进入血液循环的原形药量减少的现象是( )
A 酶抑制作用 B 首关效应 C I相代谢 D 酶诱导作用 E II相代谢
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配伍选择题 (2023年真题)氯霉素合用降糖药甲苯磺丁脲引起低血糖反应的原因是( )
A 酶抑制作用 B 首关效应 C I相代谢 D 酶诱导作用 E II相代谢
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配伍选择题 (2023年真题)结构为氨基双膦酸盐,用于治疗骨质疏松的药物是( )
A A.米诺膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442791_0.png"> B B.依替膦酸二钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442791_0_1.png"> C C.唑来膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442791_0_2.png"> D D.阿仑膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442791_0_3.png"> E E.利塞膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442791_0_4.png">
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配伍选择题 (2023年真题)结构为吡啶双膦酸盐,用于治疗骨质疏松的药物是( )
A A.米诺膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442790_0.png"> B B.依替膦酸二钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442790_0_1.png"> C C.唑来膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442790_0_2.png"> D D.阿仑膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442790_0_3.png"> E E.利塞膦酸钠<img border="0" alt="" src="https://tuku.weimei168.com/uploads/upimg/20240322/21442790_0_4.png">
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配伍选择题 (2023年真题)反映单次给药后,口服吸收程度的药动学参数是( )
A A B B C C D D E E
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