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It covers prescription review, drug interactions, adverse reactions, dosage principles, and medication storage, with structured prompts and target responses for supervised fine-tuning. It can support training and evaluation of pharmacy knowledge question answering and medication safety understanding.\u003C\u002Fp>","2026-10-16 11:52:20","2026-10-19 17:18:40","0.00",0,5000,"pharmacy QA dataset,medication safety data,pharmacist exam questions,prescription review QA,drug interactions,adverse drug reactions,pharmacy SFT data,pharmacy knowledge training","Pharmacy questions and explanations covering prescription review, drug interactions, adverse reactions, dosage, and storage for domain fine-tuning and safety QA","JSON","0.2GB","pharmacy practice education, prescription review, medication safety training","pharmacy question answering, prescription interpretation, medication risk and safety reasoning","V1.0","rivo\u002Fsample-packages\u002Fb8022e62-f71b-4e2a-b567-1a31ba73f699\u002F20261016.zip",[583,588,594,599,604,610],{"id":572,"name":584,"field":585,"intro":586,"type":587},"File Name","file_name","File name","string",{"id":589,"name":590,"field":591,"intro":592,"type":593},9639,"Source QA Content","source_qa","Original questions and explanations collected from pharmacist certification or pharmacy practice resources.","object",{"id":595,"name":596,"field":597,"intro":598,"type":587},9640,"SFT User Prompt","sft_prompt","A model input prompt composed from the source question and answer options for supervised fine-tuning.",{"id":600,"name":601,"field":602,"intro":603,"type":587},9641,"SFT Target Response","sft_response","A normalized pharmacy QA response based on the standard answer and its explanation.",{"id":605,"name":606,"field":607,"intro":608,"type":609},9642,"Knowledge Topics","knowledge_topics","Pharmacy topics inferred from the question and explanation, such as prescription review, drug interactions, adverse reactions, dosage principles, or medication storage.","array",{"id":611,"name":612,"field":613,"intro":614,"type":609},9643,"Medication Safety Risk Points","safety_risk_points","Potential medication risks, contraindications, monitoring requirements, or safety precautions identified in the QA content.",[616,620,624,628],{"id":617,"question":618,"answer":619},6681,"Which pharmacy topics are covered?","The dataset covers pharmacy practice and medication safety topics such as prescription review, drug interactions, adverse reactions, dosage principles, and medication storage, with questions and answer explanations.",{"id":621,"question":622,"answer":623},6682,"How are the examples structured?","Records include source QA content, a user prompt and target response for supervised fine-tuning, plus structured knowledge topics and medication safety risk points. Refer to the dataset version for the exact record schema.",{"id":625,"question":626,"answer":627},6683,"What applications is this dataset suitable for?","It can support supervised fine-tuning of pharmacy QA models, pharmacist exam preparation tools, QA system evaluation, and medication risk identification research. For real-world care, qualified professionals should verify model outputs; the dataset is not a standalone basis for diagnosis or prescribing.",{"id":629,"question":630,"answer":631},6684,"How can I access the data and check its license?","Check the dataset product page for access instructions, version details, and license terms. Because the content originates from web-based practice resources, confirm the applicable permissions and comply with relevant copyright and data use requirements before use.",[633,646,656],{"id":634,"relate_table":635,"relate_id":636,"file_size":572,"file_name":637,"path":8,"duration":572,"cate":483,"file_format":638,"audio_rate":8,"audio_channel":522,"audio_bit_depth":522,"quality":8,"annotation":639,"cate_name":640,"source_qa":641,"sft_prompt":642,"sft_response":643,"knowledge_topics":644,"safety_risk_points":645},15321,"union_cubo",1281900362,"样例_3.json","json","{\"source_qa\": \"{\\\"question\\\": \\\"During prescription review, it is found that the patient is taking simvastatin, and clarithromycin has also been prescribed. What is the most appropriate action for the pharmacist?\\\", \\\"options\\\": [\\\"A. Double the clarithromycin dose directly to offset the interaction\\\", \\\"B. Tell the patient that the two drugs can be used together long term without monitoring\\\", \\\"C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own\\\", \\\"D. As long as the patient has no muscle aches, continue using the original prescription\\\"], \\\"answer\\\": \\\"C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own\\\", \\\"explanation\\\": \\\"Clarithromycin can inhibit CYP3A4, potentially increasing simvastatin exposure and increasing the risk of serious adverse reactions such as myopathy and rhabdomyolysis. During prescription review, the prescribing physician should be contacted promptly, and based on the specific infection situation and patient risk, an alternative antibacterial drug should be evaluated or lipid-lowering therapy adjusted; the combination should not be continued merely because symptoms are temporarily absent, nor should the patient stop or change medications on their own.\\\"}\", \"sft_prompt\": \"Please address the following drug interaction from the perspective of prescription review: The patient is using simvastatin, and clarithromycin has also been prescribed. A. Double the clarithromycin dose directly to offset the interaction; B. Tell the patient that the two drugs can be used together long term without monitoring; C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own; D. As long as the patient has no muscle aches, continue using the original prescription.\", \"sft_response\": \"Correct answer: C. Clarithromycin can inhibit CYP3A4, increasing simvastatin exposure and thereby increasing the risk of myopathy and rhabdomyolysis. Pharmacists should identify this interaction during prescription review and contact the prescribing physician to evaluate an alternative antibacterial drug or adjust lipid-lowering therapy. Patients should not combine, stop, or change medications on their own. The absence of immediate muscle symptoms does not rule out risk.\", \"knowledge_topics\": \"[\\\"Prescription review\\\", \\\"Drug interactions\\\", \\\"CYP3A4 enzyme inhibition\\\", \\\"Statin adverse reactions\\\"]\", \"safety_risk_points\": \"[\\\"Clarithromycin may increase simvastatin plasma exposure\\\", \\\"Concomitant use of the two drugs can increase the risk of myopathy and rhabdomyolysis\\\", \\\"When a high-risk interaction is found during prescription review, contact the prescribing physician to evaluate and adjust\\\", \\\"Temporary absence of symptoms cannot be used as a basis to exclude interaction risk\\\"]\"}","文本","{\"question\": \"During prescription review, it is found that the patient is taking simvastatin, and clarithromycin has also been prescribed. What is the most appropriate action for the pharmacist?\", \"options\": [\"A. Double the clarithromycin dose directly to offset the interaction\", \"B. Tell the patient that the two drugs can be used together long term without monitoring\", \"C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own\", \"D. As long as the patient has no muscle aches, continue using the original prescription\"], \"answer\": \"C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own\", \"explanation\": \"Clarithromycin can inhibit CYP3A4, potentially increasing simvastatin exposure and increasing the risk of serious adverse reactions such as myopathy and rhabdomyolysis. During prescription review, the prescribing physician should be contacted promptly, and based on the specific infection situation and patient risk, an alternative antibacterial drug should be evaluated or lipid-lowering therapy adjusted; the combination should not be continued merely because symptoms are temporarily absent, nor should the patient stop or change medications on their own.\"}","Please address the following drug interaction from the perspective of prescription review: The patient is using simvastatin, and clarithromycin has also been prescribed. A. Double the clarithromycin dose directly to offset the interaction; B. Tell the patient that the two drugs can be used together long term without monitoring; C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own; D. As long as the patient has no muscle aches, continue using the original prescription.","Correct answer: C. Clarithromycin can inhibit CYP3A4, increasing simvastatin exposure and thereby increasing the risk of myopathy and rhabdomyolysis. Pharmacists should identify this interaction during prescription review and contact the prescribing physician to evaluate an alternative antibacterial drug or adjust lipid-lowering therapy. Patients should not combine, stop, or change medications on their own. The absence of immediate muscle symptoms does not rule out risk.","[\"Prescription review\", \"Drug interactions\", \"CYP3A4 enzyme inhibition\", \"Statin adverse reactions\"]","[\"Clarithromycin may increase simvastatin plasma exposure\", \"Concomitant use of the two drugs can increase the risk of myopathy and rhabdomyolysis\", \"When a high-risk interaction is found during prescription review, contact the prescribing physician to evaluate and adjust\", \"Temporary absence of symptoms cannot be used as a basis to exclude interaction risk\"]",{"id":647,"relate_table":635,"relate_id":648,"file_size":572,"file_name":649,"path":8,"duration":572,"cate":483,"file_format":638,"audio_rate":8,"audio_channel":522,"audio_bit_depth":522,"quality":8,"annotation":650,"cate_name":640,"source_qa":651,"sft_prompt":652,"sft_response":653,"knowledge_topics":654,"safety_risk_points":655},15320,1481985168,"样例_2.json","{\"source_qa\": \"{\\\"question\\\": \\\"Regarding the storage of unopened insulin preparations, which of the following practices is most appropriate?\\\", \\\"options\\\": [\\\"A. Store in the freezer to extend the expiration date\\\", \\\"B. Refrigerate at 2-8°C as required by the instructions, avoid freezing, and follow the temperature and usage period specified in the instructions during use\\\", \\\"C. Keep in direct sunlight for a long time for easy access at any time\\\", \\\"D. Storage temperature may fluctuate frequently and widely, as long as the liquid has not changed color\\\"], \\\"answer\\\": \\\"B. Refrigerate at 2-8°C as required by the instructions, avoid freezing, and follow the temperature and usage period specified in the instructions during use\\\", \\\"explanation\\\": \\\"Most unopened insulin preparations should be refrigerated as required by the instructions, usually at 2-8°C, and should be protected from freezing, excessive heat, and light. Freezing or exposure to excessively high temperatures may cause the drug to become ineffective; even if the appearance has not changed significantly, this cannot be used to confirm that quality is unaffected. The storage temperature and usable period of opened insulin vary by specific preparation and device and should be based on the drug instructions.\\\"}\", \"sft_prompt\": \"Please answer the storage management question for insulin preparations and explain the reason: Regarding the storage of unopened insulin preparations, which of the following practices is most appropriate? A. Store in the freezer to extend the expiration date; B. Refrigerate at 2-8°C as required by the instructions, avoid freezing, and follow the temperature and usage period specified in the instructions during use; C. Keep in direct sunlight for a long time for easy access at any time; D. Storage temperature may fluctuate frequently and widely, as long as the liquid has not changed color.\", \"sft_response\": \"Correct answer: B. Unopened insulin should generally be refrigerated at 2-8°C according to the drug instructions, and protected from freezing, excessive heat, and light. Freezing or high temperatures may affect drug quality; it cannot be determined that the drug is still effective solely because the appearance has not changed color. The storage conditions and usable period of opened insulin depend on the specific preparation and delivery device and should be based on the instructions.\", \"knowledge_topics\": \"[\\\"Storage management\\\", \\\"Insulin preparation management\\\", \\\"Cold-chain drug safety\\\", \\\"Drug efficacy protection\\\"]\", \"safety_risk_points\": \"[\\\"Insulin should avoid freezing and high-temperature exposure\\\", \\\"Unopened preparations usually need to be refrigerated according to the instructions\\\", \\\"The storage period and conditions of opened preparations vary by product\\\", \\\"Drug quality after improper temperature storage cannot be judged solely by appearance\\\"]\"}","{\"question\": \"Regarding the storage of unopened insulin preparations, which of the following practices is most appropriate?\", \"options\": [\"A. Store in the freezer to extend the expiration date\", \"B. Refrigerate at 2-8°C as required by the instructions, avoid freezing, and follow the temperature and usage period specified in the instructions during use\", \"C. Keep in direct sunlight for a long time for easy access at any time\", \"D. Storage temperature may fluctuate frequently and widely, as long as the liquid has not changed color\"], \"answer\": \"B. Refrigerate at 2-8°C as required by the instructions, avoid freezing, and follow the temperature and usage period specified in the instructions during use\", \"explanation\": \"Most unopened insulin preparations should be refrigerated as required by the instructions, usually at 2-8°C, and should be protected from freezing, excessive heat, and light. Freezing or exposure to excessively high temperatures may cause the drug to become ineffective; even if the appearance has not changed significantly, this cannot be used to confirm that quality is unaffected. The storage temperature and usable period of opened insulin vary by specific preparation and device and should be based on the drug instructions.\"}","Please answer the storage management question for insulin preparations and explain the reason: Regarding the storage of unopened insulin preparations, which of the following practices is most appropriate? A. Store in the freezer to extend the expiration date; B. Refrigerate at 2-8°C as required by the instructions, avoid freezing, and follow the temperature and usage period specified in the instructions during use; C. Keep in direct sunlight for a long time for easy access at any time; D. Storage temperature may fluctuate frequently and widely, as long as the liquid has not changed color.","Correct answer: B. Unopened insulin should generally be refrigerated at 2-8°C according to the drug instructions, and protected from freezing, excessive heat, and light. Freezing or high temperatures may affect drug quality; it cannot be determined that the drug is still effective solely because the appearance has not changed color. The storage conditions and usable period of opened insulin depend on the specific preparation and delivery device and should be based on the instructions.","[\"Storage management\", \"Insulin preparation management\", \"Cold-chain drug safety\", \"Drug efficacy protection\"]","[\"Insulin should avoid freezing and high-temperature exposure\", \"Unopened preparations usually need to be refrigerated according to the instructions\", \"The storage period and conditions of opened preparations vary by product\", \"Drug quality after improper temperature storage cannot be judged solely by appearance\"]",{"id":657,"relate_table":635,"relate_id":658,"file_size":572,"file_name":659,"path":8,"duration":572,"cate":483,"file_format":638,"audio_rate":8,"audio_channel":522,"audio_bit_depth":522,"quality":8,"annotation":660,"cate_name":640,"source_qa":661,"sft_prompt":662,"sft_response":663,"knowledge_topics":664,"safety_risk_points":665},15319,1953985270,"样例_1.json","{\"source_qa\": \"{\\\"question\\\": \\\"The patient is taking warfarin and wants to self-add ibuprofen for joint pain. During prescription review or medication counseling, what risk requires the greatest attention?\\\", \\\"options\\\": [\\\"A. Decreased anticoagulant effect, leading to increased risk of thrombosis\\\", \\\"B. Increased bleeding risk\\\", \\\"C. Severe hypoglycemia\\\", \\\"D. Drug-induced cataract\\\"], \\\"answer\\\": \\\"B. Increased bleeding risk\\\", \\\"explanation\\\": \\\"Ibuprofen is a nonsteroidal anti-inflammatory drug that can inhibit platelet function and damage the gastrointestinal mucosa; when used with warfarin, it may additively increase bleeding risk. During medication review, attention should be paid to whether unnecessary concomitant use exists, and the patient should be advised not to self-add ibuprofen; if concomitant use is truly necessary, a physician or pharmacist should evaluate alternative regimens and bleeding manifestations, and monitoring should be performed as required.\\\"}\", \"sft_prompt\": \"Please determine the main safety risk of the following medication combination and explain the reason: The patient is taking warfarin and wants to self-add ibuprofen for joint pain. Options: A. Decreased anticoagulant effect, leading to increased risk of thrombosis; B. Increased bleeding risk; C. Severe hypoglycemia; D. Drug-induced cataract.\", \"sft_response\": \"Correct answer: B. Increased bleeding risk. Ibuprofen can inhibit platelet function and damage the gastrointestinal mucosa, and concomitant use with warfarin may produce an additive bleeding risk. Patients should not combine the drugs on their own; if concomitant use is truly necessary, a physician or pharmacist should evaluate alternative regimens, and bleeding manifestations and relevant coagulation indicators should be monitored as appropriate.\", \"knowledge_topics\": \"[\\\"Drug interactions\\\", \\\"Anticoagulant medication safety\\\", \\\"Prescription review\\\", \\\"Nonsteroidal anti-inflammatory drug risks\\\"]\", \"safety_risk_points\": \"[\\\"Concomitant use of warfarin and ibuprofen can increase bleeding risk\\\", \\\"Nonsteroidal anti-inflammatory drugs may cause gastrointestinal mucosal injury and affect platelet function\\\", \\\"Patients should not self-add medications that may affect anticoagulation safety\\\", \\\"When necessary, monitor bleeding symptoms and coagulation-related indicators\\\"]\"}","{\"question\": \"The patient is taking warfarin and wants to self-add ibuprofen for joint pain. During prescription review or medication counseling, what risk requires the greatest attention?\", \"options\": [\"A. Decreased anticoagulant effect, leading to increased risk of thrombosis\", \"B. Increased bleeding risk\", \"C. Severe hypoglycemia\", \"D. Drug-induced cataract\"], \"answer\": \"B. Increased bleeding risk\", \"explanation\": \"Ibuprofen is a nonsteroidal anti-inflammatory drug that can inhibit platelet function and damage the gastrointestinal mucosa; when used with warfarin, it may additively increase bleeding risk. During medication review, attention should be paid to whether unnecessary concomitant use exists, and the patient should be advised not to self-add ibuprofen; if concomitant use is truly necessary, a physician or pharmacist should evaluate alternative regimens and bleeding manifestations, and monitoring should be performed as required.\"}","Please determine the main safety risk of the following medication combination and explain the reason: The patient is taking warfarin and wants to self-add ibuprofen for joint pain. Options: A. Decreased anticoagulant effect, leading to increased risk of thrombosis; B. Increased bleeding risk; C. Severe hypoglycemia; D. Drug-induced cataract.","Correct answer: B. Increased bleeding risk. Ibuprofen can inhibit platelet function and damage the gastrointestinal mucosa, and concomitant use with warfarin may produce an additive bleeding risk. Patients should not combine the drugs on their own; if concomitant use is truly necessary, a physician or pharmacist should evaluate alternative regimens, and bleeding manifestations and relevant coagulation indicators should be monitored as appropriate.","[\"Drug interactions\", \"Anticoagulant medication safety\", \"Prescription review\", \"Nonsteroidal anti-inflammatory drug risks\"]","[\"Concomitant use of warfarin and ibuprofen can increase bleeding risk\", \"Nonsteroidal anti-inflammatory drugs may cause gastrointestinal mucosal injury and affect platelet function\", \"Patients should not self-add medications that may affect anticoagulation safety\", \"When necessary, monitor bleeding symptoms and coagulation-related indicators\"]","{\"source_qa\":\"{\\\"question\\\": \\\"During prescription review, it is found that the patient is taking simvastatin, and clarithromycin has also been prescribed. What is the most appropriate action for the pharmacist?\\\", \\\"options\\\": [\\\"A. Double the clarithromycin dose directly to offset the interaction\\\", \\\"B. Tell the patient that the two drugs can be used together long term without monitoring\\\", \\\"C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own\\\", \\\"D. As long as the patient has no muscle aches, continue using the original prescription\\\"], \\\"answer\\\": \\\"C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own\\\", \\\"explanation\\\": \\\"Clarithromycin can inhibit CYP3A4, potentially increasing simvastatin exposure and increasing the risk of serious adverse reactions such as myopathy and rhabdomyolysis. During prescription review, the prescribing physician should be contacted promptly, and based on the specific infection situation and patient risk, an alternative antibacterial drug should be evaluated or lipid-lowering therapy adjusted; the combination should not be continued merely because symptoms are temporarily absent, nor should the patient stop or change medications on their own.\\\"}\",\"sft_prompt\":\"Please address the following drug interaction from the perspective of prescription review: The patient is using simvastatin, and clarithromycin has also been prescribed. A. Double the clarithromycin dose directly to offset the interaction; B. Tell the patient that the two drugs can be used together long term without monitoring; C. Identify the potential interaction and contact the prescribing physician to evaluate an alternative regimen or adjust treatment, and prevent the patient from combining the drugs on their own; D. As long as the patient has no muscle aches, continue using the original prescription.\",\"sft_response\":\"Correct answer: C. Clarithromycin can inhibit CYP3A4, increasing simvastatin exposure and thereby increasing the risk of myopathy and rhabdomyolysis. Pharmacists should identify this interaction during prescription review and contact the prescribing physician to evaluate an alternative antibacterial drug or adjust lipid-lowering therapy. Patients should not combine, stop, or change medications on their own. The absence of immediate muscle symptoms does not rule out risk.\",\"knowledge_topics\":\"[\\\"Prescription review\\\", \\\"Drug interactions\\\", \\\"CYP3A4 enzyme inhibition\\\", \\\"Statin adverse reactions\\\"]\",\"safety_risk_points\":\"[\\\"Clarithromycin may increase simvastatin plasma exposure\\\", \\\"Concomitant use of the two drugs can increase the risk of myopathy and rhabdomyolysis\\\", \\\"When a high-risk interaction is found during prescription review, contact the prescribing physician to evaluate and adjust\\\", \\\"Temporary absence of symptoms cannot be used as a basis to exclude interaction risk\\\"]\"}","MOBIUSI INC","https:\u002F\u002Fstatic.mobiusi.com\u002Fmobiwusi\u002F20250829\u002F7bf4ac62b4533e2b809998a6f1c5491e.png?Expires=1792463130&OSSAccessKeyId=LTAI5tH8MQqhgeiAtrzCHrxM&Signature=v6Tr8jBrdm4s5wU1SnnyGsYg%2Bhw%3D&x-oss-process=image%2Fresize%2Cm_fill%2Cw_35%2Ch_35",[670,676],{"type":671,"title":672,"count_data":673},"bar","Length distribution",[674],{"name":675,"value":483},"1k lower",{"type":677,"title":678,"count_data":679},"pie","Language distribution",[680],{"name":681,"value":483},"English"]