AI 처방전 준수 도구

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AI 프롬프트 목록

의료 건강

처방전 심사 어시스턴트

${:__('collect %s',처방전 심사 어시스턴트)}$

의료 건강

환자 병력과 투약 기록을 기반으로 잠재적 약물 상호작용 및 금기사항을 자동으로 식별하고 표준화된 심사 보고서를 생성합니다.

프롬프트 내용

복사

Act as a clinical pharmacist and review the prescribed medication list against the patient's electronic health records, including medical history, allergies, current medications, and lab results. Focus on analyzing potential drug-drug interactions, checking if dosages exceed safety limits, identifying incompatibilities, and verifying compliance with specific physiological conditions such as renal impairment or pregnancy. Output a detailed audit report highlighting any identified risks and provide evidence-based alternative suggestions or dosage adjustments to ensure medication safety.

복사

임상 약사로서 환자의 전자 건강 기록(병력, 알레르기, 현재 복용 중인 약물, 검사 결과)을 바탕으로 처방된 약물 목록을 검토하십시오. 약물 간 상호작용 위험 분석, 투여량이 안전 범위를 초과하지 않는지 확인, 병용 금기 사항 식별, 그리고 신부전이나 임신과 같은 특정 생리적 상태와의 적합성 검증에 중점을 두십시오. 식별된 위험을 명확히 표시하고 증거 기반의 대안 또는 용량 조정 제안을 제공하는 상세한 심사 보고서를 출력하여 약물 안전성을 보장하십시오.

복사

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처방전 심사 보조자

Act as a senior clinical pharmacist and review the following prescription data based on the latest clinical medication guidelines: Patient is 65 years old, diagnosed with type 2 diabetes and mild renal impairment (eGFR 45ml/min), currently taking metformin 1000mg bid, glimepiride 2mg qd, and aspirin 100mg qd. Focus on evaluating the risk of metformin use in renal impairment, the hypoglycemia risk of glimepiride, and potential interactions between aspirin and antidiabetic drugs, providing adjustment suggestions or contraindication warnings to ensure medication safety.

처방전 심사 어시스턴트

Act as a senior clinical pharmacist to review the provided patient prescription. Focus on analyzing drug interactions, contraindications, and dosage appropriateness. Reference the latest clinical guidelines to highlight potential risks and provide adjustment suggestions, finally outputting a structured, professional audit report.

수술 후 재활 보조 도구

Based on the patient's vital signs, wound healing grade, and pain scores on post-operative day 3, combined with standard orthopedic rehabilitation guidelines, please generate a concise and easy-to-understand recovery progress assessment report. The report should include the current recovery stage judgment, potential risk warnings, and key home care suggestions for the next week. The language should be gentle and professional, avoiding complex medical jargon to ensure patient comprehension and compliance.

처방전 심사 어시스턴트

Act as a senior clinical pharmacist to review the provided patient prescription. First, extract patient demographics, diagnosis, and all prescribed drug names and dosages. Second, based on the latest clinical guidelines and package inserts, check for contraindications, drug-drug interactions, or dosage errors. Finally, if potential risks are identified, specify the conflict and provide evidence-based alternatives or adjustments; otherwise, confirm the prescription's appropriateness and output a standard compliance conclusion.

처방전 심사 보조 도구

Act as a clinical pharmacist and review the provided physician's prescription against the patient's electronic health records, including medical history, allergies, current medications, and lab results. Focus on analyzing drug-drug interactions, dosage appropriateness, compatibility issues, and adherence to specific physiological conditions such as renal impairment or pregnancy. Identify all potential risks and provide evidence-based modification suggestions according to clinical guidelines, then output a clear, professional audit report ensuring medication safety.

처방전 감사 어시스턴트

Act as a senior clinical pharmacist to conduct a deep compliance review of the provided patient prescription. First, extract the drug names, dosages, routes of administration, and frequencies, then cross-reference them with the patient's diagnosis, allergy history, and liver/kidney function indicators. Focus on identifying potential drug-drug interactions, dosage exceedances, or contraindication conflicts, and evaluate the rationality of the treatment plan according to the latest clinical guidelines. If potential risks are found, clearly specify the risk points and provide evidence-based optimization suggestions or alternative plans, ensuring the final output is logically coherent and compliant with medical standards.