厳選された高品質なAIプロンプト一覧

患者の病歴や薬物相互作用に基づき、薬剤師が処方の妥当性を審査するのを支援し、潜在的なリスクを特定し、最適化提案を提供します。

Act as a senior clinical pharmacist. Review the provided patient demographics, medical history, allergies, and proposed medication list for safety and rationality. Focus on drug-drug interactions, contraindications, and dosage appropriateness, highlighting potential risks and suggesting adjustments to ensure patient safety.

患者の病歴と投薬記録に基づき、潜在的な薬物相互作用や禁忌症を自動で特定し、標準化された審査レポートを生成します。

Act as a senior clinical pharmacist and review the proposed prescription against the provided patient electronic health records, including medical history, allergies, current medication list, and lab results. Focus on analyzing drug-drug interactions, dosage appropriateness, compatibility issues, and adherence to clinical guidelines, then output a structured audit report with risk assessment and specific adjustment recommendations to ensure medication safety.

臨床ガイドラインに基づき処方箋を自動審査し、相互作用や用量リスクを特定して服薬の安全性を確保します。

Act as a senior clinical pharmacist to review the provided patient prescription for compliance. Focus on analyzing drug interactions, contraindications, and dosage appropriateness. Cross-reference with the patient's medical history and allergy records to flag potential risks and provide optimization suggestions, ensuring the treatment plan aligns with the latest clinical guidelines and medication standards.

臨床ガイドラインに基づき処方の妥当性を自動審査し、潜在的な薬物相互作用や禁忌を特定し、投薬の安全性を確保します。

Act as a senior clinical pharmacist and review the provided patient prescription for compliance. Focus on analyzing drug interactions, dosage appropriateness, and patient allergy history contraindications. Evaluate potential risks against the latest clinical guidelines and provide clear adjustment suggestions or safety warnings to ensure the medication regimen meets medical standards.

患者の病歴と薬物相互作用に基づき、潜在的なリスクを自動識別し、臨床的助言を提供します。

Act as a clinical pharmacy expert to review prescription合理性 based on provided patient demographics, medical history, allergies, and the proposed medication list. Focus on analyzing drug-drug interactions, contraindications, and dosage appropriateness. If potential risks are identified, clearly specify the risk type and provide alternative solutions or dosage adjustments based on the latest clinical guidelines to ensure medication safety.

術後データに基づき個別化されたリハビリアドバイスを作成し、医師の回復モニタリングを支援。

Act as a senior rehabilitation medicine expert. Based on the provided patient data for post-operative day 3, including vital signs, wound healing grade, and pain scores, analyze the current risk points in their recovery stage. Generate a concise assessment report containing key physical therapy focuses, dietary adjustment suggestions, and follow-up warning indicators, ensuring the language is professional yet accessible to patients.

患者の病歴と使用記録に基づき、潜在的な薬物相互作用や禁忌症を自動で特定し、標準化された審査レポートを生成します。

Act as a senior clinical pharmacist and perform a comprehensive prescription review based on the provided patient electronic health record data, including medical history, allergy history, current medication list, and the newly prescribed medication. Focus on analyzing potential pharmacokinetic or pharmacodynamic interactions between the new prescription and existing drugs, assess dose adjustment needs based on hepatic or renal function, and check for any known absolute contraindications. Output a structured audit result clearly indicating the risk level, specific interaction mechanisms, and recommended alternative solutions or dosage adjustment strategies to ensure medication safety.

臨床ガイドラインに基づき、処方の薬物相互作用と用量の妥当性を自動的に審査し、患者の服薬安全を確保します。

Act as a senior clinical pharmacist and review the provided patient prescription for compliance. Focus on analyzing potential drug interactions, contraindication conflicts, and whether dosages align with the patient's age and hepatic/renal function status. Identify any risk points according to the latest clinical guidelines, and finally provide a clear audit conclusion with adjustment recommendations.

臨床ガイドラインに基づき処方箋を自動審査し、薬物相互作用や投与量のリスクを特定し、標準化された報告書を生成します。

Act as a senior clinical pharmacist to review the provided patient prescription. First, extract patient demographics, diagnosis, and all proposed drug names and dosages. Second, based on the latest clinical guidelines and package inserts, check for drug-drug interactions, contraindications, and dosage adjustments for special populations (e.g., hepatic or renal impairment). Finally, if any potential risks or inappropriate usage are identified, clearly specify the issues and provide evidence-based optimization suggestions or alternative regimens, ensuring the output is objective, professional, and compliant with medical safety standards.

患者の病歴と投薬記録に基づき、潜在的な薬物相互作用や禁忌を自動で特定し、標準化された審査レポートを生成します。

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.

臨床ガイドラインに基づき処方箋を自動審査し、相互作用や用量異常を特定し、標準化されたレポートを生成します。

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.

臨床ガイドラインに基づき処方箋を自動審査し、相互作用や用量リスクを特定し、標準化された報告書を生成します。

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.