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SUBJECT: Patient experiencing side effects on Atorvastatin - medical information and adverse event documentation BODY: Dear Medical Information and Commercial Team, I am a emergency physician writing on behalf of a 58 year old female patient who has been on Atorvastatin. The therapy was initiated 2 weeks ago at a dose ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by severe proximal muscle pain, dark cola-colored urine, and profound weak...
SUBJECT: Medical information request and adverse event report for Metformin BODY: Dear Healthcare Information and Quality Assurance Team, I am a hospitalist writing on behalf of a 62 year old male patient who has been on Metformin. Treatment was started approximately 10 days ago with 100 mg per day. In the 1 week lead...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by megaloblastic anemia with hemoglobin dropping to 9.2 g/dL, accompanied by ...
SUBJECT: Urgent: adverse reaction to Lisinopril with concurrent clinical question BODY: Dear Clinical Affairs and Business Development Team, I am a consultant writing on behalf of a 80 year old male patient who has been on Lisinopril. Treatment was started approximately 14 days ago with 100 mg per day. Approximately 1...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by creatinine rising from 1.1 mg/dL to 4.2 mg/dL within 5 days of initiation...
SUBJECT: Adverse reaction to Amoxicillin - clinical guidance and medical information request BODY: Dear Scientific Information and Supply Chain Teams, I am a pathologist writing on behalf of a 54 year old female patient who has been on Amoxicillin. The prescribed regimen is 20 mg and the patient commenced therapy 14 da...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by fatigue, oral ulcers, and recurrent infections with WBC 2.1 x10^9/L, hem...
SUBJECT: Safety report and clinical guidance needed for Amlodipine adverse reaction BODY: Dear Medical Information and Product Integrity Team, I am a pathologist writing on behalf of a 29 year old female patient who has been on Amlodipine. Treatment was started approximately 5 weeks ago with 12.5 mg per day. During th...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by severe sunburn-like reaction after brief outdoor exposure, with erythema,...
SUBJECT: Urgent: adverse reaction to Amoxicillin with concurrent clinical question BODY: Dear Scientific Information and Supply Chain Teams, I am a surgeon writing on behalf of a 67 year old male patient who has been on Amoxicillin. The therapy was initiated 3 weeks ago at a dose of 100 mg. In the 5 days leading up to...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by generalized tonic-clonic seizures occurring on day 4 of therapy in a pat...
SUBJECT: Patient safety concern and information request - Amoxicillin related BODY: Dear Medical Information and Safety Team, I am writing as the husband of a 71 year old female patient who is taking Amoxicillin. Treatment was started approximately 9 weeks ago with 5 mg per day. Over the past 8 days, she developed fat...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by fatigue, oral ulcers, and recurrent infections with WBC 2.1 x10^9/L, hem...
SUBJECT: Patient safety concern and information request - Ibuprofen related BODY: Dear Healthcare Information and Quality Assurance Team, I am writing as the wife of a 50 year old female patient who is taking Ibuprofen. The prescribed regimen is 5 mg and she commenced therapy 7 weeks ago. During the past 3 weeks, she ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Ibuprofen, a non-company product, evidenced by creatinine rising from 0.9 mg/dL to 3.4 mg/dL over 10 days of high-dose us...
SUBJECT: Side effects from Amlodipine and a dosing question BODY: Dear Medical Information and Safety Team, I am a anaesthesiologist writing on behalf of a 29 year old male patient who has been on Amlodipine. the patient has been on this medication for 12 weeks at 40 mg daily. Over the past 2 weeks, the patient develo...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by severe gingival overgrowth covering 60% of tooth surfaces causing bleedin...
SUBJECT: Side effects from Amlodipine and a dosing question BODY: Dear Medical Affairs and Quality Department, I am a pulmonologist writing on behalf of a 70 year old female patient who has been on Amlodipine. The prescribed regimen is 150 mcg and the patient commenced therapy 9 weeks ago. In the 4 days leading up to ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by palpitations with resting heart rate of 110 bpm, chest discomfort, anxiet...
SUBJECT: Patient experiencing toxicity concerns on Levothyroxine - medical information and adverse event documentation BODY: Dear Medical Affairs and Quality Department, I am a plastic surgeon writing on behalf of a 71 year old female patient who has been on Levothyroxine. The prescribed regimen is 80 mg and the patien...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by agitation, paranoid delusions, visual hallucinations, and pressured sp...
SUBJECT: Urgent: adverse reaction to Amoxicillin with concurrent clinical question BODY: Dear Medical Information and Product Integrity Team, I am a endocrinologist writing on behalf of a 76 year old male patient who has been on Amoxicillin. The prescribed regimen is 80 mg and the patient commenced therapy 10 days ago....
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by generalized tonic-clonic seizures occurring on day 4 of therapy in a pat...
SUBJECT: Methotrexate related adverse event report and clinical inquiry BODY: Dear Medical Affairs and Quality Department, I am a psychiatrist writing on behalf of a 16 year old male patient who has been on Methotrexate. The therapy was initiated 2 weeks ago at a dose of 250 mg. During the past 9 days, the patient pre...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by fever, oral ulcers, and sepsis with CBC showing WBC 1.8 x10^9/L, hemogl...
SUBJECT: Urgent: adverse reaction to Metformin with concurrent clinical question BODY: Dear Medical Information and Product Integrity Team, I am a surgeon writing on behalf of a 83 year old female patient who has been on Metformin. the patient has been on this medication for 3 months at 15 mg daily. Approximately 9 da...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by complete loss of appetite, early satiety, and unintended weight loss of 8 ...
SUBJECT: Urgent: adverse reaction to Atorvastatin with concurrent clinical question BODY: Dear Clinical and Product Safety Teams, I am a intensivist writing on behalf of a 85 year old male patient who has been on Atorvastatin. The prescribed regimen is 40 mg and the patient commenced therapy 21 days ago. Approximately...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by jaundice with bilirubin 3.2 mg/dL, ALT 340 U/L, and alkaline phosphatas...
SUBJECT: Adverse event documentation and dosing guidance for Omeprazole BODY: Dear Medical Affairs and Pharmacovigilance Team, I am writing as the husband of a 55 year old female patient who is taking Omeprazole. The therapy was initiated 3 months ago at a dose of 80 mg. In the 2 weeks leading up to this report, she s...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by right femoral neck fracture after a minor fall from standing height with ...
SUBJECT: Adverse reaction to Omeprazole - clinical guidance and medical information request BODY: Dear Scientific Information and Supply Chain Teams, I am a dr. writing on behalf of a 62 year old male patient who has been on Omeprazole. the patient has been on this medication for 21 days at 500 mg daily. During the pa...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by severe muscle spasms, carpopedal tetany, and ventricular arrhythmia with ...
SUBJECT: Clinical query and adverse event notification - Ibuprofen therapy BODY: Dear Medical Information and Safety Team, I am a cardiologist writing on behalf of a 16 year old male patient who has been on Ibuprofen. the patient has been on this medication for 14 days at 5 mg daily. In the 4 days leading up to this r...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Ibuprofen, a non-company product, evidenced by painful mucosal erosions of the oral cavity and conjunctivae, targetoid sk...
SUBJECT: Clinical query and adverse event notification - Metformin therapy BODY: Dear Scientific Information and Supply Chain Teams, I am a nurse practitioner reporting on behalf of a 75 year old male patient under our care who has been prescribed Metformin. Treatment was started approximately 3 months ago with 10 mg p...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by platelet count dropped to 68 x10^9/L with petechial rash and epistaxis dev...
SUBJECT: Safety report and clinical guidance needed for Metformin adverse reaction BODY: Dear Medical Information and Regulatory Affairs Team, I am a gp writing on behalf of a 37 year old female patient who has been on Metformin. The therapy was initiated 8 weeks ago at a dose of 15 mg. During the past 12 days, the pa...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by persistent vomiting up to 8 times daily, watery diarrhea, and abdominal bl...
SUBJECT: Urgent: adverse reaction to Methotrexate with concurrent clinical question BODY: Dear Medical Information and Product Integrity Team, I am a physician assistant writing on behalf of a 50 year old male patient who has been on Methotrexate. Treatment was started approximately 5 weeks ago with 25 mg per day. App...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by severe oral ulcerations extending to the esophagus, preventing oral int...
SUBJECT: Medical information request and adverse event report for Amoxicillin BODY: Dear Clinical Affairs and Business Development Team, I am a nurse practitioner reporting on behalf of a 49 year old male patient under our care who has been prescribed Amoxicillin. The prescribed regimen is 12.5 mg and the patient comme...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by pruritus, jaundice, dark urine, and pale stools with bilirubin 5.8 mg/dL...
SUBJECT: Adverse event documentation and dosing guidance for Lisinopril BODY: Dear Medical Information and Product Integrity Team, I am writing as the daughter of a 45 year old male patient who is taking Lisinopril. he has been on this medication for 5 months at 30 mg daily. In the 12 days leading up to this report, h...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by persistent dry nonproductive cough occurring day and night, disturbing sl...
SUBJECT: Levothyroxine related adverse event report and clinical inquiry BODY: Dear Clinical Affairs and Business Development Team, I am a 29 year old male patient and I have been prescribed Levothyroxine. Treatment was started approximately 21 days ago with 100 mg per day. In the 8 days leading up to this report, he ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by crushing substernal chest pain, ST elevation in anterior leads V1 thro...
SUBJECT: Medical information request and adverse event report for Ibuprofen BODY: Dear Medical Information and Regulatory Affairs Team, I am a plastic surgeon writing on behalf of a 58 year old female patient who has been on Ibuprofen. The therapy was initiated 3 months ago at a dose of 80 mg. During the past 10 days,...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Ibuprofen, a non-company product, evidenced by severe headache, neck stiffness, photophobia, and fever with normal CSF ba...
SUBJECT: Safety report and clinical guidance needed for Levothyroxine adverse reaction BODY: Dear Medical Information and Product Integrity Team, I am a gastroenterologist writing on behalf of a 75 year old female patient who has been on Levothyroxine. The prescribed regimen is 12.5 mg and the patient commenced therapy...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by chronic loose stools, steatorrhea, and weight loss of 6 kg with low fe...
SUBJECT: Adverse event documentation and dosing guidance for Methotrexate BODY: Dear Clinical and Product Safety Teams, I am a nurse reporting on behalf of a 76 year old female patient under our care who has been prescribed Methotrexate. The therapy was initiated 3 weeks ago at a dose of 125 mcg. Over the past 12 days...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by severe oral ulcerations extending to the esophagus, preventing oral int...
SUBJECT: Side effects from Metformin and a dosing question BODY: Dear Clinical Affairs and Business Development Team, I am a hospitalist writing on behalf of a 65 year old female patient who has been on Metformin. The therapy was initiated 4 months ago at a dose of 150 mcg. Over the past 6 days, the patient developed ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by profound weakness, nausea, abdominal discomfort, and Kussmaul respirations...
SUBJECT: Urgent: adverse reaction to Ibuprofen with concurrent clinical question BODY: Dear Scientific Information and Supply Chain Teams, I am a 50 year old male patient and I have been prescribed Ibuprofen. he has been on this medication for 12 weeks at 2.5 mg daily. Over the past 14 days, he developed painful mucos...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Ibuprofen, a non-company product, evidenced by painful mucosal erosions of the oral cavity and conjunctivae, targetoid sk...
SUBJECT: Safety report and clinical guidance needed for Omeprazole adverse reaction BODY: Dear Medical Information and Safety Team, I am writing as the husband of a 62 year old female patient who is taking Omeprazole. Treatment was started approximately 14 days ago with 30 mg per day. In the 6 days leading up to this ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by macrocytic anemia with MCV 108 fL, hemoglobin 9.6 g/dL, and serum B12 of ...
SUBJECT: Safety report and clinical guidance needed for Levothyroxine adverse reaction BODY: Dear Medical Information and Regulatory Affairs Team, I am a cardiologist writing on behalf of a 41 year old male patient who has been on Levothyroxine. The prescribed regimen is 250 mg and the patient commenced therapy 5 weeks...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by severe exercise limitation, dyspnea on mild exertion, and resting tach...
SUBJECT: Adverse event documentation and dosing guidance for Amlodipine BODY: Dear Medical Information and Commercial Team, I am a hospitalist writing on behalf of a 32 year old female patient who has been on Amlodipine. Treatment was started approximately 14 days ago with 15 mg per day. Approximately 5 days ago, the ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by palpitations with resting heart rate of 110 bpm, chest discomfort, anxiet...
SUBJECT: Adverse event documentation and dosing guidance for Methotrexate BODY: Dear Medical Information and Safety Team, I am a pathologist writing on behalf of a 65 year old male patient who has been on Methotrexate. The therapy was initiated 5 weeks ago at a dose of 2000 mg. During the past 5 days, the patient pres...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by severe oral ulcerations extending to the esophagus, preventing oral int...
SUBJECT: Patient experiencing therapy-related adverse event on Amlodipine - medical information and adverse event documentation BODY: Dear Medical Affairs and Quality Department, I am a intensivist writing on behalf of a 55 year old female patient who has been on Amlodipine. the patient has been on this medication for ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by new-onset low mood, anhedonia, psychomotor retardation, and early morning...
SUBJECT: Urgent: adverse reaction to Methotrexate with concurrent clinical question BODY: Dear Medical Information and Safety Team, I am writing as the wife of a 49 year old male patient who is taking Methotrexate. The therapy was initiated 5 weeks ago at a dose of 7.5 mg. Approximately 6 days ago, he began experienci...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by new cervical lymphadenopathy, B symptoms with night sweats and 4 kg wei...
SUBJECT: Adverse event documentation and dosing guidance for Omeprazole BODY: Dear Medical Affairs and Quality Department, I am a hematologist writing on behalf of a 80 year old female patient who has been on Omeprazole. The therapy was initiated 1 month ago at a dose of 50 mg. During the past 10 days, the patient pre...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by rapid cognitive decline over 18 months with MMSE falling from 28 to 19, e...
SUBJECT: Safety report and clinical guidance needed for Levothyroxine adverse reaction BODY: Dear Medical Affairs and Quality Department, I am a anaesthesiologist writing on behalf of a 41 year old female patient who has been on Levothyroxine. the patient has been on this medication for 12 weeks at 30 mg daily. During...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by crushing substernal chest pain, ST elevation in anterior leads V1 thro...
SUBJECT: Side effects from Methotrexate and a dosing question BODY: Dear Medical Information and Commercial Team, I am a charge nurse reporting on behalf of a 45 year old male patient under our care who has been prescribed Methotrexate. Treatment was started approximately 4 months ago with 25 mg per day. During the pa...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by jaundice, fatigue, pruritus, and hepatomegaly with liver biopsy showing...
SUBJECT: Urgent: adverse reaction to Amoxicillin with concurrent clinical question BODY: Dear Medical Information and Product Integrity Team, I am a radiologist writing on behalf of a 16 year old female patient who has been on Amoxicillin. Treatment was started approximately 5 months ago with 100 mg per day. In the 6 ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by rapidly progressive erythema, blistering, and full-thickness epidermal d...
SUBJECT: Patient safety concern and information request - Lisinopril related BODY: Dear Clinical Affairs and Business Development Team, I am a clinical pharmacist and I am contacting you regarding a 44 year old male patient for whom Lisinopril was dispensed from our pharmacy. Treatment was started approximately 9 weeks...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by severe epigastric pain radiating to the back, serum lipase 1200 U/L, and ...
SUBJECT: Adverse event documentation and dosing guidance for Lisinopril BODY: Dear Medical Affairs and Quality Department, I am a 49 year old female patient and I have been prescribed Lisinopril. Treatment was started approximately 14 days ago with 7.5 mg per day. Approximately 5 days ago, she began experiencing fever...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by fever, sore throat, and severe neutropenia with absolute neutrophil count...
SUBJECT: Urgent: adverse reaction to Methotrexate with concurrent clinical question BODY: Dear Medical Information and Regulatory Affairs Team, I am a geriatrician writing on behalf of a 25 year old female patient who has been on Methotrexate. the patient has been on this medication for 9 weeks at 20 mg daily. In the ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by disseminated histoplasmosis with fever, weight loss, hepatosplenomegaly...
SUBJECT: Adverse event documentation and dosing guidance for Amoxicillin BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a neurologist writing on behalf of a 75 year old male patient who has been on Amoxicillin. Treatment was started approximately 5 months ago with 100 mg per day. In the 12 days leading up...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by rapidly progressive erythema, blistering, and full-thickness epidermal d...
SUBJECT: Adverse reaction to Levothyroxine - clinical guidance and medical information request BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a clinical pharmacist and I am contacting you regarding a 65 year old female patient for whom Levothyroxine was dispensed from our pharmacy. Treatment was started ap...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by crushing substernal chest pain, ST elevation in anterior leads V1 thro...
SUBJECT: Medical information request and adverse event report for Lisinopril BODY: Dear Clinical Affairs and Business Development Team, I am a pulmonologist writing on behalf of a 44 year old female patient who has been on Lisinopril. The prescribed regimen is 150 mcg and the patient commenced therapy 3 months ago. Du...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by flushing, urticaria, abdominal cramping, and hypotension of 76/44 mmHg wi...
SUBJECT: Medical information request and adverse event report for Lisinopril BODY: Dear Healthcare Information and Quality Assurance Team, I am a cardiologist writing on behalf of a 41 year old male patient who has been on Lisinopril. The prescribed regimen is 2000 mg and the patient commenced therapy 1 month ago. Ove...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by persistent dry nonproductive cough occurring day and night, disturbing sl...
SUBJECT: Amlodipine related adverse event report and clinical inquiry BODY: Dear Medical Affairs and Pharmacovigilance Team, I am writing as the son of a 41 year old male patient who is taking Amlodipine. The therapy was initiated 9 weeks ago at a dose of 100 mg. Approximately 1 week ago, he began experiencing new-ons...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by new-onset low mood, anhedonia, psychomotor retardation, and early morning...
SUBJECT: Patient experiencing hypersensitivity reaction on Amoxicillin - medical information and adverse event documentation BODY: Dear Clinical Affairs and Business Development Team, I am a endocrinologist writing on behalf of a 28 year old male patient who has been on Amoxicillin. the patient has been on this medicat...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by fatigue, pallor, dark urine, and jaundice with hemoglobin dropping to 7....
SUBJECT: Clinical query and adverse event notification - Omeprazole therapy BODY: Dear Clinical Affairs and Business Development Team, I am a orthopedic surgeon writing on behalf of a 55 year old female patient who has been on Omeprazole. The therapy was initiated 5 months ago at a dose of 25 mg. In the 3 weeks leadin...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by fever of 39.4 C, productive cough, right lower lobe consolidation on ches...
SUBJECT: Medical information request and adverse event report for Levothyroxine BODY: Dear Medical Information and Commercial Team, I am a geriatrician writing on behalf of a 75 year old female patient who has been on Levothyroxine. the patient has been on this medication for 9 weeks at 40 mg daily. Approximately 14 d...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by compression fracture of L2 vertebra after minor lifting with T-score -...
SUBJECT: Patient safety concern and information request - Metformin related BODY: Dear Medical Information and Regulatory Affairs Team, I am writing as the brother of a 28 year old male patient who is taking Metformin. Treatment was started approximately 6 weeks ago with 7.5 mg per day. Approximately 10 days ago, he b...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by complete loss of appetite, early satiety, and unintended weight loss of 8 ...
SUBJECT: Side effects from Atorvastatin and a dosing question BODY: Dear Clinical Affairs and Business Development Team, I am writing as the son of a 70 year old female patient who is taking Atorvastatin. Treatment was started approximately 2 weeks ago with 80 mg per day. Approximately 9 days ago, she began experienci...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by fasting glucose rising from 98 mg/dL to 142 mg/dL after 8 months of the...
SUBJECT: Side effects from Metformin and a dosing question BODY: Dear Clinical and Product Safety Teams, I am a specialist writing on behalf of a 25 year old female patient who has been on Metformin. The therapy was initiated 21 days ago at a dose of 25 mg. Approximately 1 week ago, the patient began experiencing comp...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by complete loss of appetite, early satiety, and unintended weight loss of 8 ...
SUBJECT: Adverse event documentation and dosing guidance for Amoxicillin BODY: Dear Healthcare Information and Quality Assurance Team, I am a urologist writing on behalf of a 44 year old male patient who has been on Amoxicillin. The prescribed regimen is 150 mcg and the patient commenced therapy 21 days ago. Over the ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by generalized tonic-clonic seizures occurring on day 4 of therapy in a pat...
SUBJECT: Side effects from Lisinopril and a dosing question BODY: Dear Medical Information and Commercial Team, I am a physician writing on behalf of a 76 year old female patient who has been on Lisinopril. The therapy was initiated 3 months ago at a dose of 100 mg. Approximately 1 week ago, the patient began experien...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by persistent dry nonproductive cough occurring day and night, disturbing sl...
SUBJECT: Patient safety concern and information request - Methotrexate related BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a cardiologist writing on behalf of a 70 year old male patient who has been on Methotrexate. the patient has been on this medication for 4 months at 500 mg daily. Over the past 2 w...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by severe oral ulcerations extending to the esophagus, preventing oral int...
SUBJECT: Patient safety concern and information request - Lisinopril related BODY: Dear Healthcare Information and Quality Assurance Team, I am a surgeon writing on behalf of a 62 year old male patient who has been on Lisinopril. The therapy was initiated 5 months ago at a dose of 1000 mg. During the past 8 days, the ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by sudden swelling of the tongue, lips, and larynx causing airway compromise...
SUBJECT: Safety report and clinical guidance needed for Metformin adverse reaction BODY: Dear Clinical and Product Safety Teams, I am a 55 year old female patient and I have been prescribed Metformin. The therapy was initiated 1 month ago at a dose of 50 mg. Approximately 10 days ago, she began experiencing rapid brea...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by rapid breathing, severe abdominal pain, muscle cramps, and extreme fatigue...
SUBJECT: Clinical query and adverse event notification - Amlodipine therapy BODY: Dear Scientific Information and Supply Chain Teams, I am a pathologist writing on behalf of a 60 year old male patient who has been on Amlodipine. The prescribed regimen is 1000 mg and the patient commenced therapy 10 days ago. In the 12...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by new-onset low mood, anhedonia, psychomotor retardation, and early morning...
SUBJECT: Medical information request and adverse event report for Omeprazole BODY: Dear Clinical and Product Safety Teams, I am a 75 year old male patient and I have been prescribed Omeprazole. The therapy was initiated 1 month ago at a dose of 150 mcg. Approximately 14 days ago, he began experiencing endoscopic surve...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by endoscopic surveillance revealing numerous sessile polyps in the gastric ...
SUBJECT: Patient safety concern and information request - Metformin related BODY: Dear Scientific Information and Supply Chain Teams, I am a gastroenterologist writing on behalf of a 71 year old female patient who has been on Metformin. The therapy was initiated 3 months ago at a dose of 100 mg. During the past 5 days...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by profound weakness, nausea, abdominal discomfort, and Kussmaul respirations...
SUBJECT: Adverse reaction to Methotrexate - clinical guidance and medical information request BODY: Dear Clinical and Product Safety Teams, I am writing as the mother of a 55 year old female patient who is taking Methotrexate. she has been on this medication for 21 days at 15 mg daily. In the 14 days leading up to thi...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by fever, oral ulcers, and sepsis with CBC showing WBC 1.8 x10^9/L, hemogl...
SUBJECT: Side effects from Methotrexate and a dosing question BODY: Dear Medical Information and Safety Team, I am a family medicine physician writing on behalf of a 49 year old female patient who has been on Methotrexate. the patient has been on this medication for 9 weeks at 12.5 mg daily. Over the past 10 days, the...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by severe oral ulcerations extending to the esophagus, preventing oral int...
SUBJECT: Patient safety concern and information request - Amlodipine related BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a intensivist writing on behalf of a 41 year old male patient who has been on Amlodipine. The therapy was initiated 4 months ago at a dose of 12.5 mg. In the 3 weeks leading up to th...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by severe sunburn-like reaction after brief outdoor exposure, with erythema,...
SUBJECT: Patient safety concern and information request - Amoxicillin related BODY: Dear Medical Information and Regulatory Affairs Team, I am a orthopedic surgeon writing on behalf of a 28 year old male patient who has been on Amoxicillin. Treatment was started approximately 10 days ago with 7.5 mg per day. In the 2 ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by rapidly progressive erythema, blistering, and full-thickness epidermal d...
SUBJECT: Adverse event documentation and dosing guidance for Lisinopril BODY: Dear Scientific Information and Supply Chain Teams, I am a 76 year old male patient and I have been prescribed Lisinopril. The therapy was initiated 8 weeks ago at a dose of 5 mg. Over the past 12 days, he developed jaundice, dark urine, ele...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by jaundice, dark urine, elevated ALT to 480 U/L and AST to 390 U/L with pos...
SUBJECT: Medical information request and adverse event report for Atorvastatin BODY: Dear Scientific Information and Supply Chain Teams, I am writing as the son of a 61 year old male patient who is taking Atorvastatin. he has been on this medication for 7 weeks at 250 mg daily. Over the past 3 weeks, he developed prog...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by progressive severe proximal muscle weakness with CK persistently above ...
SUBJECT: Adverse event documentation and dosing guidance for Amoxicillin BODY: Dear Medical Affairs and Quality Department, I am writing as the caregiver of a 50 year old female patient who is taking Amoxicillin. The prescribed regimen is 15 mg and she commenced therapy 14 days ago. Approximately 8 days ago, she began...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by widespread pruritic maculopapular rash involving 80% of body surface are...
SUBJECT: Clinical query and adverse event notification - Atorvastatin therapy BODY: Dear Clinical Affairs and Business Development Team, I am a charge nurse reporting on behalf of a 58 year old male patient under our care who has been prescribed Atorvastatin. The therapy was initiated 12 weeks ago at a dose of 30 mg. ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by progressive burning sensation and numbness in both feet with reduced vi...
SUBJECT: Patient safety concern and information request - Metformin related BODY: Dear Medical Information and Regulatory Affairs Team, I am writing as the wife of a 45 year old male patient who is taking Metformin. he has been on this medication for 5 weeks at 1000 mg daily. Approximately 4 days ago, he began experie...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by platelet count dropped to 68 x10^9/L with petechial rash and epistaxis dev...
SUBJECT: Metformin related adverse event report and clinical inquiry BODY: Dear Scientific Information and Supply Chain Teams, I am a charge nurse reporting on behalf of a 67 year old male patient under our care who has been prescribed Metformin. Treatment was started approximately 8 weeks ago with 50 mg per day. In t...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by severe epigastric pain radiating to the back, serum lipase 980 U/L, and am...
SUBJECT: Levothyroxine related adverse event report and clinical inquiry BODY: Dear Medical Information and Commercial Team, I am a 61 year old female patient and I have been prescribed Levothyroxine. Treatment was started approximately 2 weeks ago with 75 mcg per day. During the past 8 days, she presented with agitat...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by agitation, paranoid delusions, visual hallucinations, and pressured sp...
SUBJECT: Safety report and clinical guidance needed for Atorvastatin adverse reaction BODY: Dear Clinical and Product Safety Teams, I am writing as the wife of a 37 year old female patient who is taking Atorvastatin. The prescribed regimen is 5 mg and she commenced therapy 6 weeks ago. In the 1 week leading up to this...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by new-onset depressed mood, anhedonia, fatigue, and passive suicidal idea...
SUBJECT: Patient safety concern and information request - Amlodipine related BODY: Dear Medical Information and Regulatory Affairs Team, I am a family medicine physician writing on behalf of a 50 year old female patient who has been on Amlodipine. The prescribed regimen is 25 mg and the patient commenced therapy 5 mont...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by palpitations with resting heart rate of 110 bpm, chest discomfort, anxiet...
SUBJECT: Patient experiencing side effects on Methotrexate - medical information and adverse event documentation BODY: Dear Clinical Affairs and Business Development Team, I am writing as the mother of a 33 year old male patient who is taking Methotrexate. Treatment was started approximately 14 days ago with 150 mcg pe...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by jaundice, fatigue, pruritus, and hepatomegaly with liver biopsy showing...
SUBJECT: Adverse event documentation and dosing guidance for Levothyroxine BODY: Dear Clinical and Product Safety Teams, I am a hospitalist writing on behalf of a 70 year old male patient who has been on Levothyroxine. The prescribed regimen is 20 mg and the patient commenced therapy 6 weeks ago. Over the past 8 days,...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by irregularly irregular pulse with heart rate 140 bpm, dyspnea on exerti...
SUBJECT: Adverse event documentation and dosing guidance for Methotrexate BODY: Dear Medical Affairs and Quality Department, I am a nurse practitioner reporting on behalf of a 62 year old male patient under our care who has been prescribed Methotrexate. The therapy was initiated 3 months ago at a dose of 150 mcg. Over...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by spontaneous miscarriage at 8 weeks gestation in a patient who conceived...
SUBJECT: Patient safety concern and information request - Lisinopril related BODY: Dear Medical Information and Regulatory Affairs Team, I am a surgeon writing on behalf of a 19 year old male patient who has been on Lisinopril. The therapy was initiated 7 weeks ago at a dose of 7.5 mg. In the 12 days leading up to thi...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by creatinine rising from 1.1 mg/dL to 4.2 mg/dL within 5 days of initiation...
SUBJECT: Patient safety concern and information request - Metformin related BODY: Dear Scientific Information and Supply Chain Teams, I am a anaesthesiologist writing on behalf of a 60 year old female patient who has been on Metformin. the patient has been on this medication for 6 weeks at 20 mg daily. In the 9 days l...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by severe epigastric pain radiating to the back, serum lipase 980 U/L, and am...
SUBJECT: Adverse event documentation and dosing guidance for Amlodipine BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a physician assistant writing on behalf of a 16 year old female patient who has been on Amlodipine. The therapy was initiated 7 weeks ago at a dose of 125 mcg. During the past 9 days, the...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by bilateral pitting edema extending to the knees, with weight gain of 6 kg ...
SUBJECT: Side effects from Atorvastatin and a dosing question BODY: Dear Medical Information and Product Integrity Team, I am writing as the wife of a 52 year old female patient who is taking Atorvastatin. The therapy was initiated 8 weeks ago at a dose of 250 mg. During the past 12 days, she presented with spontaneou...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by spontaneous rupture of the left Achilles tendon during normal walking w...
SUBJECT: Clinical query and adverse event notification - Omeprazole therapy BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a 19 year old female patient and I have been prescribed Omeprazole. The therapy was initiated 2 weeks ago at a dose of 75 mcg. In the 2 weeks leading up to this report, she showed sig...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by photosensitive annular and psoriasiform plaques on the upper back, chest,...
SUBJECT: Medical information request and adverse event report for Amlodipine BODY: Dear Scientific Information and Supply Chain Teams, I am a family medicine physician writing on behalf of a 76 year old male patient who has been on Amlodipine. The prescribed regimen is 500 mg and the patient commenced therapy 12 weeks ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by bilateral pitting edema extending to the knees, with weight gain of 6 kg ...
SUBJECT: Safety report and clinical guidance needed for Atorvastatin adverse reaction BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a general practitioner writing on behalf of a 67 year old female patient who has been on Atorvastatin. The prescribed regimen is 1000 mg and the patient commenced therapy 5 w...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "98%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Atorvastatin, a non-company product, evidenced by severe proximal muscle pain, dark cola-colored urine, and profound weak...
SUBJECT: Medical information request and adverse event report for Amlodipine BODY: Dear Medical Information and Regulatory Affairs Team, I am writing as the mother of a 85 year old female patient who is taking Amlodipine. she has been on this medication for 14 days at 5 mg daily. During the past 2 weeks, she presented...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by severe gingival overgrowth covering 60% of tooth surfaces causing bleedin...
SUBJECT: Clinical query and adverse event notification - Methotrexate therapy BODY: Dear Medical Information and Product Integrity Team, I am writing as the son of a 58 year old female patient who is taking Methotrexate. The therapy was initiated 10 days ago at a dose of 2000 mg. Approximately 10 days ago, she began e...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by oliguria, rising creatinine from 0.9 to 5.4 mg/dL, and hyperkalemia fol...
SUBJECT: Amoxicillin related adverse event report and clinical inquiry BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a psychiatrist writing on behalf of a 16 year old male patient who has been on Amoxicillin. the patient has been on this medication for 14 days at 100 mg daily. Approximately 10 days ago, ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by fatigue, oral ulcers, and recurrent infections with WBC 2.1 x10^9/L, hem...
SUBJECT: Omeprazole related adverse event report and clinical inquiry BODY: Dear Healthcare Information and Quality Assurance Team, I am a emergency physician writing on behalf of a 58 year old male patient who has been on Omeprazole. Treatment was started approximately 12 weeks ago with 12.5 mg per day. Over the past...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by profuse watery diarrhea 14 times per day, fever of 38.5 C, leukocytosis o...
SUBJECT: Adverse event documentation and dosing guidance for Ibuprofen BODY: Dear Medical Affairs and Quality Department, I am writing as the mother of a 52 year old male patient who is taking Ibuprofen. The therapy was initiated 9 weeks ago at a dose of 125 mcg. In the 10 days leading up to this report, he showed sig...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Ibuprofen, a non-company product, evidenced by blood pressure surge to 198/116 mmHg with headache, chest pain, and papill...
SUBJECT: Side effects from Amoxicillin and a dosing question BODY: Dear Medical Affairs and Pharmacovigilance Team, I am writing as the sister of a 61 year old male patient who is taking Amoxicillin. The prescribed regimen is 40 mg and he commenced therapy 8 weeks ago. During the past 3 weeks, he presented with fever,...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amoxicillin, a non-company product, evidenced by fever, rash, eosinophilia of 2200 per microliter, and acute kidney injur...
SUBJECT: Adverse reaction to Levothyroxine - clinical guidance and medical information request BODY: Dear Medical Affairs and Quality Department, I am writing as the wife of a 52 year old female patient who is taking Levothyroxine. The prescribed regimen is 25 mg and she commenced therapy 5 months ago. In the 6 days l...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Levothyroxine, a non-company product, evidenced by crushing substernal chest pain, ST elevation in anterior leads V1 thro...
SUBJECT: Metformin related adverse event report and clinical inquiry BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a charge nurse reporting on behalf of a 29 year old male patient under our care who has been prescribed Metformin. Treatment was started approximately 14 days ago with 100 mg per day. Approx...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by profound weakness, nausea, abdominal discomfort, and Kussmaul respirations...
SUBJECT: Side effects from Ibuprofen and a dosing question BODY: Dear Clinical and Product Safety Teams, I am a plastic surgeon writing on behalf of a 65 year old female patient who has been on Ibuprofen. The therapy was initiated 14 days ago at a dose of 30 mg. Approximately 12 days ago, the patient began experiencin...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Ibuprofen, a non-company product, evidenced by progressive fatigue, pallor, recurrent infections, and bleeding with bone ...
SUBJECT: Safety report and clinical guidance needed for Methotrexate adverse reaction BODY: Dear Medical Information and Regulatory Affairs Team, I am a hospitalist writing on behalf of a 70 year old female patient who has been on Methotrexate. the patient has been on this medication for 7 weeks at 1000 mg daily. Appr...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Methotrexate, a non-company product, evidenced by headache, visual disturbances, seizures, and altered mental status with...
SUBJECT: Clinical query and adverse event notification - Lisinopril therapy BODY: Dear Healthcare Information and Quality Assurance Team, I am a nurse practitioner reporting on behalf of a 52 year old male patient under our care who has been prescribed Lisinopril. Treatment was started approximately 8 weeks ago with 15...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "94%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Lisinopril, a non-company product, evidenced by flushing, urticaria, abdominal cramping, and hypotension of 76/44 mmHg wi...
SUBJECT: Patient experiencing side effects on Metformin - medical information and adverse event documentation BODY: Dear Medical Information and Safety Team, I am a cardiologist writing on behalf of a 75 year old male patient who has been on Metformin. The prescribed regimen is 12.5 mg and the patient commenced therapy...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Metformin, a non-company product, evidenced by complete loss of appetite, early satiety, and unintended weight loss of 8 ...
SUBJECT: Patient safety concern and information request - Amlodipine related BODY: Dear Scientific Information and Supply Chain Teams, I am a neonatologist writing on behalf of a 61 year old female patient who has been on Amlodipine. Treatment was started approximately 8 weeks ago with 5 mg per day. Approximately 9 da...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by bilateral pitting edema extending to the knees, with weight gain of 6 kg ...
SUBJECT: Patient safety concern and information request - Omeprazole related BODY: Dear Medical Information and Product Integrity Team, I am writing as the caregiver of a 19 year old female patient who is taking Omeprazole. The prescribed regimen is 100 mg and she commenced therapy 4 months ago. During the past 4 days...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Omeprazole, a non-company product, evidenced by profuse watery diarrhea 14 times per day, fever of 38.5 C, leukocytosis o...
SUBJECT: Safety report and clinical guidance needed for Amlodipine adverse reaction BODY: Dear Medical Information and Commercial Team, I am a pathologist writing on behalf of a 55 year old female patient who has been on Amlodipine. the patient has been on this medication for 6 weeks at 100 mg daily. During the past 1...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "95%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by persistent facial erythema, warmth, and burning sensation resembling rosa...
SUBJECT: Medical information request and adverse event report for Amlodipine BODY: Dear Medical Affairs and Pharmacovigilance Team, I am a urologist writing on behalf of a 25 year old female patient who has been on Amlodipine. The therapy was initiated 5 months ago at a dose of 2.5 mg. During the past 2 weeks, the pat...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "93%"}, "Analysis": "The email reports new adverse symptoms temporally associated with Amlodipine, a non-company product, evidenced by severe gingival overgrowth covering 60% of tooth surfaces causing bleedin...
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Medical Emails Multi-Label Classification Dataset

This dataset contains 1000 synthetic medical emails for multi-label classification across 5 combined categories.

Categories (200 emails each)

Category Count Description
Adverse Event + Medical Information 200 Emails reporting adverse symptoms while also requesting clinical/scientific information
Medical Information + Product Complaint 200 Emails requesting clinical guidance while also reporting product quality defects
Medical Information + Other 200 Emails requesting clinical information while also making B2B commercial inquiries
Adverse Event + Product Complaint 200 Emails reporting adverse reactions while also documenting product quality issues
All Four Combined 200 Emails containing adverse event, medical information request, product complaint, and B2B inquiry in a single message

Non-Company Product X List

All emails reference one of these 9 non-company drugs:

  • Metformin, Atorvastatin, Amoxicillin, Ibuprofen, Omeprazole, Lisinopril, Levothyroxine, Amlodipine, Methotrexate

Format

Strict JSONL with 2 fields per line:

  • instruction: Email subject and body (structured as "SUBJECT: ...\nBODY:\n...")
  • output: JSON string containing classification result and analysis

Example

{"instruction":"SUBJECT: Side effects from Metformin and a dosing question\nBODY:\nDear Medical Information Team,\nI have been taking Metformin 500mg for my type 2 diabetes for approximately 3 weeks. Over the past 10 days I have been experiencing severe and persistent nausea...","output":"{\"Classification_of_request\": {\"Classification\": \"Adverse Event, Medical Information\", \"Confidence_percentage\": \"95%\"}, \"Analysis\": \"The email reports new adverse symptoms temporally associated with initiation of Metformin...\"}"}

Dataset Characteristics

  • Total emails: 1000 (all unique)
  • Senders: Mixed HCPs (physicians, nurses, pharmacists, specialists) and non-HCPs (patients, caregivers)
  • Numeric normalization: All numbers written as digits (e.g., "45 year old", "500 mg", "3 weeks")
  • No unicode escape characters: No \u2013 or similar escapes in the data
  • No parenthesis in analysis text

Generated by ML Intern

This dataset repository was generated by ML Intern, an agent for machine learning research and development on the Hugging Face Hub.

Usage

from datasets import load_dataset

dataset = load_dataset('Ramesh10/medical-emails-multilabel-dataset')
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