Datasets:

Ramesh10
/

medical-info-adverse-event-dataset

instruction stringlengths 1.72k 2.34k	output stringlengths 697 1.25k
SUBJECT: Suspected Product A adverse event with past Product B and ongoing Levothyroxine Dear Medical Affairs Division, I am writing on behalf of a patient group member to report an adverse event involving a recently initiated medication and to submit a related medical information query. I wish to report an adverse ev...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 73 year old male patient started on Product A 4 weeks ago for haemophagocytic lymphohistiocytosis who developed new visual disturbances, blurred vision, and bilateral opti...
SUBJECT: Product A side effects with ongoing Product B and Product A clinical information Dear Adverse Events Reporting Centre, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to report an ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 47 year old male patient started on Product A 13 weeks ago for sarcoidosis who developed progressive bronchiolitis obliterans with dyspnoea, fixed obs...
SUBJECT: Formal notification Product A reaction with historical Product B and medical query Dear Pharmacovigilance and Risk Management Team, I am the Consultant Pulmonologist at a large endocrinology centre and I am writing to formally report an adverse event involving a patient under my care and to request clinical in...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 38 year old female patient started on Product A 5 weeks ago for pulmonary arterial hypertension who developed profound fatigue, pallor, and symptomati...
SUBJECT: Product A reaction report with Product B previously used and Product A dose question Dear Sir or Madam, I am writing on behalf of a patient group member to report an adverse event involving a recently initiated medication and to submit a related medical information query. I wish to report an adverse event. Th...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 75 year old male patient started on Product A 12 weeks ago for dermatomyositis who developed acute kidney injury with serum creatinine rising from bas...
SUBJECT: Product A adverse event report with Product B completed course and Atorvastatin ongoing Dear Pharmacovigilance and Risk Management Team, I am the Consultant Cardiologist at a corporate occupational health provider and I am writing to formally report an adverse event involving a patient under my care and to req...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 38 year old female patient started on Product A 2 weeks ago for gout prophylaxis who developed progressive demyelinating polyneuropathy with ascending weakness, areflexia,...
SUBJECT: Product A adverse event with historical Product B and Product A information request Dear Medical and Pharmacovigilance Team, I am the Consultant Cardiologist at a hepatology referral centre and I am writing to formally report an adverse event involving a patient under my care and to request clinical informatio...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 56 year old female patient started on Product A 9 weeks ago for osteoporosis who developed progressive bronchiolitis obliterans with dyspnoea, fixed o...
SUBJECT: Product A adverse event report with Product B maintained and clinical request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Clinical Nurse Specialist at an immunology and allergy clinic and I am documenting this adverse event report on behalf of a patient under our ward care and forwa...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 39 year old male patient started on Product A 12 weeks ago for antiphospholipid syndrome who developed acute kidney injury with serum creatinine risin...
SUBJECT: Formal report involving Product A with historical Product B and background Methotrexate Dear Corporate Drug Safety and Medical Information Department, I am the Consultant Gastroenterologist at a pharmaceutical benefit manager and I am writing to formally report an adverse event involving a patient under my car...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 36 year old female patient started on Product A 13 weeks ago for ankylosing spondylitis who developed severe photosensitivity with blistering sunburn-like reaction on sun-...
SUBJECT: Product A reaction with prior Product B therapy and clinical information request Dear Regional Pharmacovigilance Lead, I am writing as the caregiver for my elderly aunt Ronald Walker to report an adverse reaction they experienced with a recently started medication and to request related clinical information. ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 35 year old male patient started on Product A 14 weeks ago for atrial fibrillation who developed acute hepatitis with alanine aminotransferase 850 U/L...
SUBJECT: Adverse event report involving Product A with Product B past use and Atorvastatin current use Dear Adverse Events Reporting Centre, I am the Consultant Dermatologist at a surgical day case unit group and I am writing to formally report an adverse event involving a patient under my care and to request clinical ...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 32 year old female patient started on Product A 11 weeks ago for chronic graft-versus-host disease who developed severe muscle weakness across both lower limbs, significan...
SUBJECT: Product A reaction with prior Product B therapy and clinical information request Dear Regional Pharmacovigilance Lead, I am the Head of Pharmacy Services at a multi-site primary care network and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also sub...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 80 year old female patient started on Product A 7 weeks ago for an autoimmune skin condition who developed severe muscle weakness across both lower li...
SUBJECT: Product A adverse event with historical Product B and concomitant Omeprazole Dear Medical and Pharmacovigilance Team, I am the Consultant Endocrinologist at a community health partnership covering 12 clinics and I am writing to formally report an adverse event involving a patient under my care and to request c...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 41 year old male patient started on Product A 14 weeks ago for interstitial lung disease who developed acute tumour lysis syndrome with hyperuricaemia, hyperkalaemia, hype...
SUBJECT: Adverse event report involving Product A with Product B past use and Omeprazole current use Dear Adverse Events Reporting Centre, I am writing as the caregiver for my elderly aunt Susan Watson to report an adverse reaction they experienced with a recently started medication and to request related clinical info...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 77 year old male patient started on Product A 8 weeks ago for glaucoma who developed progressive dyspnoea, orthopnoea, and bilateral pleural effusions on chest radiography...
SUBJECT: Adverse event to Product A while on Product B with medical information request Dear Corporate Drug Safety and Medical Information Department, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 36 year old female patient started on Product A 19 weeks ago for heart failure with reduced ejection fraction who developed a severe generalized macul...
SUBJECT: Dual suspect drug reaction Product A and Product B with Product A medical query Good morning, I am the Consultant Endocrinologist at a rehabilitation and long-term care facility and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wish t...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 61 year old male patient started on Product A 20 weeks ago for inflammatory bowel disease who developed acute rhabdomyolysis with severe myalgia, crea...
SUBJECT: Product A reaction report with Product B discontinued and Atorvastatin continued Hi, I am the Head of Pharmacy Services at a university hospital department and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting a medical information query...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 74 year old female patient started on Product A 15 weeks ago for haemophagocytic lymphohistiocytosis who developed recurrent pancreatitis with severe epigastric pain, seru...
SUBJECT: Adverse event report Product A and Product B dual suspect with Product A query Dear Medical Affairs Division, I am the Medical Director at a community health partnership covering 12 clinics and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical in...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 28 year old female patient started on Product A 16 weeks ago for rheumatoid arthritis who developed acute rhabdomyolysis with severe myalgia, creatine...
SUBJECT: Product A adverse event report with Product B concomitant and dose guidance request Dear Global Safety and Medical Affairs Unit, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 79 year old male patient started on Product A 18 weeks ago for IgA nephropathy who developed new visual disturbances, blurred vision, and bilateral op...
SUBJECT: Product A suspected reaction with Product B unchanged and Product A dose question Dear Sir or Madam, I am writing on behalf of a patient group member to report an adverse event involving a recently initiated medication and to submit a related medical information query. I wish to report an adverse event. The p...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 45 year old male patient started on Product A 18 weeks ago for fibromyalgia who developed severely elevated liver enzymes confirmed on blood testing, ...
SUBJECT: Dual adverse reaction to Product A and Product B with Product A medical query To Whom It May Concern, I am the Head of Pharmacy Services at a pharmaceutical benefit manager and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting a medical ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 40 year old female patient started on Product A 19 weeks ago for osteoporosis who developed drug-induced minimal change disease with nephrotic range p...
SUBJECT: Adverse event Product A suspect Product B concomitant with Product A query Hi, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to report an adverse event. The patient experienced a...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 59 year old male patient started on Product A 5 weeks ago for systemic sclerosis who developed progressive peripheral neuropathy affecting both hands ...
SUBJECT: Serious reaction involving both Product A and Product B and Product A guidance sought Dear Drug Safety Department, I am the Director of Clinical Services at a pathology and diagnostics consortium and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medi...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 57 year old male patient started on Product A 11 weeks ago for systemic lupus erythematosus who developed progressive dysphagia, odynophagia, and seve...
SUBJECT: Reporting a serious reaction to Product A stopped Product B last year also on Levothyroxine To Whom It May Concern, I am the Consultant Haematologist at a gastroenterology clinic partnership and I am writing to formally report an adverse event involving a patient under my care and to request clinical informati...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 70 year old female patient started on Product A 16 weeks ago for epilepsy who developed drug-induced haemolytic anaemia with haemoglobin 6, qualifying as an Adverse Event ...
SUBJECT: Adverse event to Product A after Product B discontinued with medical query Dear Corporate Drug Safety and Medical Information Department, I am the Consultant Haematologist at a gastroenterology clinic partnership and I am writing to formally report an adverse event involving a patient under my care and to requ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 66 year old female patient started on Product A 5 weeks ago for type 2 diabetes who developed progressive multifocal leukoencephalopathy with subacute...
SUBJECT: Product A reaction with concurrent Product B and clinical information query Dear Regional Pharmacovigilance Lead, I am writing as the caregiver for my elderly aunt Brian Padilla to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wis...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 65 year old male patient started on Product A 14 weeks ago for Graft-versus-host disease who developed drug-induced vasculitis with palpable purpura, ...
SUBJECT: Product A reaction report with concomitant Product B and Product A guidance sought Dear Medical Affairs Division, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to report an adver...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 28 year old female patient started on Product A 20 weeks ago for IgA nephropathy who developed acute generalised exanthematous pustulosis with sterile...
SUBJECT: Adverse event Product A suspect with historical Product B and Product A query Hi, I am the Consultant Nephrologist at a group of private outpatient clinics and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wish to report an adverse ev...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 74 year old female patient started on Product A 13 weeks ago for Behçet disease who developed recurrent pancreatitis with severe epigastric pain, seru...
SUBJECT: Product A reaction report with concomitant Product B and Product A guidance sought Dear Medical Affairs Division, I am the Ward Nurse Manager at a tertiary referral hospital and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical information request. ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 58 year old female patient started on Product A 10 weeks ago for ankylosing spondylitis who developed acute posterior reversible encephalopathy syndro...
SUBJECT: Product A side effects with ongoing Product B and Product A clinical information Dear Adverse Events Reporting Centre, I am the Consultant Endocrinologist at a respiratory medicine centre and I am writing to formally report an adverse event involving a patient under my care and to request clinical information....	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 62 year old female patient started on Product A 20 weeks ago for an autoimmune skin condition who developed progressive dyspnoea, orthopnoea, and bila...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information Team, I am the Consultant Hepatologist at an integrated care system and I am writing to formally report an adverse event involving a patient under my care and to request clinical info...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 33 year old male patient started on Product A 6 weeks ago for epilepsy who developed progressive scleroderma-like skin changes with Raynaud phenomenon...
SUBJECT: Dual drug reaction involving Product A and Product B with information request Dear Corporate Drug Safety and Medical Information Department, I am the Consultant Nephrologist at a rheumatology clinic group and I am writing to formally report an adverse event involving a patient under my care and to request clin...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 81 year old male patient started on Product A 12 weeks ago for chronic obstructive pulmonary disease who developed progressive sensorineural hearing l...
SUBJECT: Product A adverse event with historical Product B and concomitant Omeprazole Dear Medical and Pharmacovigilance Team, I am the Head of Pharmacy Services at an integrated care system and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting a...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 71 year old male patient started on Product A 15 weeks ago for plaque psoriasis who developed drug-induced vasculitis with palpable purpura, renal involvement with active ...
SUBJECT: Serious adverse event Product A with historical Product B and concomitant Methotrexate Dear Sir or Madam, I am writing as the caregiver for my father Elijah Johnson to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report a...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 75 year old male patient started on Product A 12 weeks ago for chronic migraine prophylaxis who developed drug-induced lupus erythematosus with positive antinuclear antibo...
SUBJECT: Side effects on Product A with Product B ongoing and Product A information request Dear Drug Safety Department, I am writing on behalf of a patient group member to report an adverse event involving a recently initiated medication and to submit a related medical information query. I wish to report an adverse e...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 72 year old female patient started on Product A 17 weeks ago for type 2 diabetes who developed acute psychosis with paranoid delusions, auditory hallu...
SUBJECT: Product A adverse event report with Product B historical and clinical request Dear Post-Marketing Surveillance and Medical Information Unit, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product....	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 69 year old male patient started on Product A 15 weeks ago for plaque psoriasis who developed severe hyperglycaemia with fasting glucose 16 mmol/L, Hb...
SUBJECT: Suspected Product A adverse event with past Product B and ongoing Metformin Dear Medical Affairs Division, I am the Consultant Rheumatologist at a multi-site primary care network and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wish ...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 73 year old male patient started on Product A 9 weeks ago for chronic migraine prophylaxis who developed syncopal episodes, documented bradycardia with heart rate 33 bpm, ...
SUBJECT: Product A reaction with prior Product B therapy and clinical information request Dear Regional Pharmacovigilance Lead, I am the Medical Director at a Veterans Affairs medical centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical informatio...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 35 year old male patient started on Product A 11 weeks ago for acute graft-versus-host disease who developed acute colonic perforation with pneumoperi...
SUBJECT: Formal notification Product A reaction with concomitant Product B and medical query Dear Pharmacovigilance and Risk Management Team, I am the Chief of Medicine at a rehabilitation and long-term care facility and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a con...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 53 year old male patient started on Product A 2 weeks ago for ulcerative colitis maintenance who developed severe depression with suicidal ideation, i...
SUBJECT: Pharmacovigilance report Product A with Product B historical and Methotrexate concomitant Dear Post-Marketing Surveillance and Medical Information Unit, I am the Consultant Gastroenterologist at a pharmaceutical benefit manager and I am writing to formally report an adverse event involving a patient under my c...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 54 year old female patient started on Product A 9 weeks ago for systemic sclerosis who developed severely elevated liver enzymes confirmed on blood testing, persistent nau...
SUBJECT: Formal report involving Product A with historical Product B and background Lisinopril Dear Corporate Drug Safety and Medical Information Department, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same ...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 66 year old female patient started on Product A 7 weeks ago for multiple sclerosis relapse prevention who developed drug-induced lupus erythematosus with positive antinucl...
SUBJECT: Formal notification Product A reaction with concomitant Product B and medical query Dear Pharmacovigilance and Risk Management Team, I am writing as the caregiver for my father Hazel Gomez to report an adverse reaction they experienced with a recently started medication and to request related clinical informat...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 68 year old female patient started on Product A 7 weeks ago for systemic sclerosis who developed progressive bronchiolitis obliterans with dyspnoea, f...
SUBJECT: Adverse event Product A suspect with historical Product B and Product A query Hi, I am the Consultant Hepatologist at a paediatric outpatient service and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wish to report an adverse event. T...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 29 year old male patient started on Product A 20 weeks ago for haemophagocytic lymphohistiocytosis who developed severe muscle weakness across both lo...
SUBJECT: Product A adverse event report with Product B historical and clinical request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Clinical Nurse Specialist at a university hospital department and I am documenting this adverse event report on behalf of a patient under our ward care and forwa...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 84 year old female patient started on Product A 3 weeks ago for fibromyalgia who developed drug-induced Sweet syndrome with fever, neutrophilia, and t...
SUBJECT: Product A reaction report with Product B discontinued and Amlodipine continued Hi, I am the Director of Clinical Services at a rural district hospital and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information request. I wish to report an...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 74 year old female patient started on Product A 8 weeks ago for polymyositis who developed acute necrotising fasciitis with severe pain out of proportion, crepitus on exam...
SUBJECT: Product A side effects with ongoing Product B and Product A clinical information Dear Adverse Events Reporting Centre, I am the Director of Clinical Services at a community health partnership covering 12 clinics and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 32 year old female patient started on Product A 9 weeks ago for polymyositis who developed recurrent pancreatitis with severe epigastric pain, serum l...
SUBJECT: Product A suspected reaction with Product B unchanged and Product A dose question Dear Sir or Madam, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to report an adverse event. The...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 45 year old male patient started on Product A 19 weeks ago for systemic sclerosis who developed acute psychosis with paranoid delusions, auditory hall...
SUBJECT: Product A adverse event with Product B concomitant and Product A medical query Dear Medical and Pharmacovigilance Team, I am writing as the caregiver for my wife Anna Torres to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 71 year old male patient started on Product A 18 weeks ago for gout prophylaxis who developed drug-induced vasculitis with palpable purpura, renal inv...
SUBJECT: Both medications suspected with Product A dosing question Hi, I am writing as the caregiver for my elderly aunt Maria Chen to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report a serious adverse event where the treating ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 74 year old female patient started on Product A 17 weeks ago for heart failure with reduced ejection fraction who developed progressive dyspnoea, orth...
SUBJECT: Formal report Product A adverse event with historical Product B and Product A query Good morning, I am the Consultant Rheumatologist at a private oncology clinic group and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wish to report a...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 46 year old female patient started on Product A 6 weeks ago for membranous nephropathy who developed new visual disturbances, blurred vision, and bila...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information Team, I am the Consultant Dermatologist at a large endocrinology centre and I am writing to formally report an adverse event involving a patient under my care and to request clinical ...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 33 year old male patient started on Product A 7 weeks ago for axial spondyloarthritis who developed acute confusion, fever to 40, qualifying as an Adv...
SUBJECT: Product A and Product B both implicated with Product A clinical query Dear Clinical Safety and Regulatory Affairs, I am the Consultant Nephrologist at a faith-based hospital system and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wis...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 67 year old male patient started on Product A 13 weeks ago for depression who developed acute myocarditis with chest pain, elevated troponin 2182 ng/L...
SUBJECT: Product A adverse event with Product B concomitant and Product A medical query Dear Medical and Pharmacovigilance Team, I am the Consultant Pulmonologist at a specialist dermatology centre and I am writing to formally report an adverse event involving a patient under my care and to request clinical information...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 41 year old male patient started on Product A 10 weeks ago for diabetic neuropathy who developed acute necrotising fasciitis with severe pain out of p...
SUBJECT: Product A adverse event with historical Product B and concomitant Atorvastatin Dear Medical and Pharmacovigilance Team, I am the Consultant Hepatologist at a managed care organisation and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I ...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 71 year old male patient started on Product A 8 weeks ago for epilepsy who developed severe depression with suicidal ideation, insomnia, and anhedonia requiring urgent psy...
SUBJECT: Adverse event Product A suspect Product B concomitant with Product A query Hi, I am writing on behalf of a patient group member to report an adverse event involving a recently initiated medication and to submit a related medical information query. I wish to report an adverse event. The patient experienced a 7...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 74 year old female patient started on Product A 10 weeks ago for vasculitis who developed acute disseminated intravascular coagulation with prolonged ...
SUBJECT: Pharmacovigilance report Product A with Product B historical and Amoxicillin concomitant Dear Post-Marketing Surveillance and Medical Information Unit, I am the Director of Clinical Services at a specialist neurology centre and I am formally notifying you of an adverse event report requiring pharmacovigilance ...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 69 year old male patient started on Product A 7 weeks ago for antiphospholipid syndrome who developed progressive dysphagia, odynophagia, and severe oesophageal ulceration...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information Team, I am the Consultant Cardiologist at an integrated care system and I am writing to formally report an adverse event involving a patient under my care and to request clinical info...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 78 year old female patient started on Product A 20 weeks ago for chronic obstructive pulmonary disease who developed severely elevated liver enzymes c...
SUBJECT: Product A reaction report with Product B discontinued and Atorvastatin continued Hi, I am the Consultant Nephrologist at a home healthcare nursing agency and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wish to report an adverse even...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 29 year old male patient started on Product A 4 weeks ago for depression who developed new-onset atrial fibrillation with rapid ventricular response, palpitations, and dys...
SUBJECT: Reporting a serious reaction to Product A stopped Product B last year also on Levothyroxine To Whom It May Concern, I am the Consultant Haematologist at a Veterans Affairs medical centre and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. ...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 55 year old male patient started on Product A 8 weeks ago for Sweet syndrome who developed severe abdominal pain, bloody diarrhoea more than 10 episodes per day, and colit...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information Team, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wis...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 48 year old female patient started on Product A 12 weeks ago for granulomatosis with polyangiitis who developed drug-induced lupus erythematosus with ...
SUBJECT: Dual adverse reaction to Product A and Product B with Product A medical query To Whom It May Concern, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to report a serious adverse ev...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 55 year old male patient started on Product A 10 weeks ago for type 2 diabetes who developed anaphylaxis within 10 minutes of dosing including urticar...
SUBJECT: Suspected Product A reaction with Product B historical and Product A medical query Dear Patient Safety and Medical Information Team, I am the Senior Nurse Practitioner at a private oncology clinic group and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a c...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 63 year old male patient started on Product A 2 weeks ago for depression who developed progressive sensorineural hearing loss with high-frequency thre...
SUBJECT: Product A and Product B reaction report with clinical information request Dear Global Safety and Medical Affairs Unit, I am the Medical Director at a specialist neurology centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information re...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 49 year old male patient started on Product A 10 weeks ago for haemophagocytic lymphohistiocytosis who developed drug-induced pneumonitis with dyspnoe...
SUBJECT: Product A adverse event report with Product B completed course and Atorvastatin ongoing Dear Pharmacovigilance and Risk Management Team, I am the Consultant Pulmonologist at a specialist neurology centre and I am writing to formally report an adverse event involving a patient under my care and to request clini...	{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 83 year old male patient started on Product A 11 weeks ago for inflammatory bowel disease who developed acute hepatitis with alanine aminotransferase 1638 U/L, bilirubin 6...
SUBJECT: Suspected adverse events with both Product A and Product B and medical query Dear Regional Pharmacovigilance Lead, I am writing as the caregiver for my brother Rebecca Fisher to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish t...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 80 year old female patient started on Product A 3 weeks ago for membranous nephropathy who developed acute necrotising fasciitis with severe pain out ...
SUBJECT: Formal report both Product A and Product B suspect with Product A dose question Dear Patient Safety and Medical Information Team, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 33 year old male patient started on Product A 17 weeks ago for Sweet syndrome who developed severe arthralgia involving multiple joints with morning s...
SUBJECT: Dual adverse reaction to Product A and Product B with Product A medical query To Whom It May Concern, I am writing to report an adverse reaction I have experienced with a medication I was recently prescribed and to request some clinical information about the same product. I wish to report a serious adverse ev...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 25 year old male patient started on Product A 4 weeks ago for juvenile idiopathic arthritis who developed acute myocarditis with chest pain, elevated ...
SUBJECT: Formal adverse event notification for Product A and Product B with medical information Dear Pharmacovigilance and Risk Management Team, I am writing on behalf of a patient group member to report an adverse event involving a recently initiated medication and to submit a related medical information query. I wis...	{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 53 year old male patient started on Product A 14 weeks ago for glaucoma who developed recurrent pancreatitis with severe epigastric pain, serum lipase...

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Ramesh10/medical-info-adverse-event-dataset

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Usage

from datasets import load_dataset

dataset = load_dataset('Ramesh10/medical-info-adverse-event-dataset')

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