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SUBJECT: Adverse event Product A suspect Product B concomitant with Product A query Hi, I am the Director of Clinical Services at a faith-based hospital system 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, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 29 year old male patient started on Product A 16 weeks ago for acute graft-versus-host disease who developed new-onset atrial fibrillation with rapid ...
SUBJECT: Product A reaction report with concomitant Product B and Product A guidance sought Dear Medical Affairs Division, I am the Consultant Gastroenterologist at a cancer centre 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, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 73 year old male patient started on Product A 12 weeks ago for heart failure with reduced ejection fraction who developed drug-induced minimal change ...
SUBJECT: Product A and Product B adverse reaction with Product A clinical information request Dear Sir or Madam, I am writing as the caregiver for my husband Frank Vasquez to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report a s...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 75 year old male patient started on Product A 14 weeks ago for ankylosing spondylitis who developed drug-induced Sweet syndrome with fever, neutrophil...
SUBJECT: Formal report both Product A and Product B suspect with Product A dose question Dear Patient Safety and Medical Information 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 concur...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 48 year old female patient started on Product A 13 weeks ago for plaque psoriasis who developed severe hyperglycaemia with fasting glucose 19 mmol/L, ...
SUBJECT: Product A suspected reaction with Product B unchanged and Product A dose question Dear Sir or Madam, I am the Head of Pharmacy Services at a group of private outpatient clinics and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting a medi...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 30 year old female patient started on Product A 14 weeks ago for ulcerative colitis maintenance who developed progressive multifocal leukoencephalopat...
SUBJECT: Formal adverse event notification for Product A and Product B with medical information Dear Pharmacovigilance and Risk Management Team, I am the Attending Physician at a community health partnership covering 12 clinics and I am formally notifying you of an adverse event report requiring pharmacovigilance revie...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 68 year old female patient started on Product A 12 weeks ago for granulomatosis with polyangiitis who developed profound fatigue, pallor, and symptoma...
SUBJECT: Formal report Product A reaction with Product B historical and Amoxicillin concomitant Dear Drug Safety 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. I wish to report an adv...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 72 year old female patient started on Product A 12 weeks ago for haemophagocytic lymphohistiocytosis who developed progressive scleroderma-like skin changes with Raynaud p...
SUBJECT: Product A reaction report with concomitant Product B and Product A guidance sought Dear Medical Affairs Division, I am writing as the caregiver for my husband Tyler Jimenez 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 28 year old female patient started on Product A 19 weeks ago for interstitial lung disease who developed acute rhabdomyolysis with severe myalgia, cre...
SUBJECT: Reporting a serious reaction to Product A stopped Product B last year also on Ibuprofen To Whom It May Concern, 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 information. I wish t...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 25 year old male patient started on Product A 2 weeks ago for diabetic neuropathy who developed severe thrombocytopenia with platelet count 17 x10^9/L and mucosal bleeding...
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 Pulmonologist at a community health partnership covering 12 clinics and I am writing to formally report an adverse event involving a patient under my car...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 51 year old male patient started on Product A 17 weeks ago for Graft-versus-host disease who developed progressive scleroderma-like skin changes with ...
SUBJECT: Both medications suspected with Product A dosing question Hi, I am the Consultant Neurologist 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. I wish to report a serious adverse event where the treati...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 29 year old male patient started on Product A 20 weeks ago for focal segmental glomerulosclerosis who developed severe muscle weakness across both low...
SUBJECT: Formal notification Product A reaction with historical Product B and medical query Dear Pharmacovigilance and Risk Management Team, I am writing as the caregiver for my brother Keith Richardson to report an adverse reaction they experienced with a recently started medication and to request related clinical inf...
{"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 8 weeks ago for primary biliary cholangitis who developed acute angle-closure glaucoma with severe ocu...
SUBJECT: Formal report involving Product A with historical Product B and background Lisinopril Dear Corporate Drug Safety and Medical Information Department, I am the Director of Clinical Services at a Veterans Affairs medical 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 51 year old male patient started on Product A 16 weeks ago for psoriatic arthritis who developed progressive dysphagia, odynophagia, and severe oesophageal ulceration on e...
SUBJECT: Formal report Product A adverse event with historical Product B and Product A query Good morning, I am the Consultant Rheumatologist 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 wish to report an ad...
{"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 3 weeks ago for ulcerative colitis maintenance who developed acute posterior reversible encephalopathy...
SUBJECT: Product A adverse event report with Product B historical and clinical request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Pharmacy Operations Manager at a hepatology referral centre and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy se...
{"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 19 weeks ago for psoriatic arthritis who developed severe photosensitivity with blistering sunburn-lik...
SUBJECT: Serious adverse event Product A with historical Product B and concomitant Methotrexate Dear Sir or Madam, I am the Consultant Pulmonologist 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 ...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 60 year old female patient started on Product A 2 weeks ago for primary biliary cholangitis who developed progressive dysphagia, odynophagia, and severe oesophageal ulcera...
SUBJECT: Formal report Product A adverse event with concomitant Product B and Product A query Good morning, I am writing as the caregiver for my elderly aunt Gary Clark to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report an adv...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 76 year old female patient started on Product A 7 weeks ago for asthma maintenance who developed syncopal episodes, documented bradycardia with heart ...
SUBJECT: Product A reaction with concurrent Product B and clinical information query Dear Regional Pharmacovigilance Lead, I am the Attending Physician at a group of private outpatient clinics and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical informat...
{"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 2 weeks ago for pulmonary arterial hypertension who developed severe muscle weakness across both lower l...
SUBJECT: Product A suspected with Product B historical and Product A clinical guidance sought Dear Medical Affairs Division, I am the Consultant Hepatologist at a pathology and diagnostics consortium 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, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 28 year old female patient started on Product A 18 weeks ago for haemophagocytic lymphohistiocytosis who developed new visual disturbances, blurred vi...
SUBJECT: Product A adverse event report with historical Product B and guidance request Dear Global Safety and Medical Affairs Unit, I am the Consultant Dermatologist at a regional hospital trust 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 64 year old female patient started on Product A 7 weeks ago for Parkinson disease who developed severe thrombocytopenia with platelet count 20 x10^9/L...
SUBJECT: Product A and Product B both suspected with Product A information request Dear Medical and Pharmacovigilance 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 report a serio...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 71 year old male patient started on Product A 3 weeks ago for heart failure with reduced ejection fraction who developed acute agranulocytosis with ab...
SUBJECT: Product A adverse event with prior Product B and concurrent Amlodipine report Dear Regional Pharmacovigilance Lead, 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 adver...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 80 year old female patient started on Product A 20 weeks ago for Crohn disease who developed drug-induced vasculitis with palpable purpura, renal involvement with active u...
SUBJECT: Suspected reaction to Product A with Product B historical and Metformin maintained Dear Clinical Safety and Regulatory Affairs, I am the Consultant Endocrinologist at an immunology and allergy clinic 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 52 year old female patient started on Product A 8 weeks ago for psoriatic arthritis who developed new-onset shortness of breath, dry cough, and bilateral pulmonary infiltr...
SUBJECT: Product A reaction report with Product B previously used and Product A dose question Dear Sir or Madam, I am the Consultant Nephrologist at a large academic medical centre and I am writing to formally report an adverse event involving a patient under my care and to request clinical information. I wish to repo...
{"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 4 weeks ago for membranous nephropathy who developed progressive restrictive cardiomyopathy with diastol...
SUBJECT: Side effects on Product A and a dosing question previously on Product B 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 an adverse event. The pati...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 55 year old male patient started on Product A 10 weeks ago for glaucoma who developed drug-induced minimal change disease with nephrotic range protein...
SUBJECT: Product A reaction report with Product B previously used and Product A dose question Dear Sir or Madam, I am writing as the caregiver for my mother Dennis Morgan to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report an a...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 60 year old female patient started on Product A 8 weeks ago for vasculitis who developed acute psychosis with paranoid delusions, auditory hallucinati...
SUBJECT: Product A adverse event report with Product B maintained and clinical request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Consultant Dermatologist at a residential care home network managing over 400 elderly residents across 5 facilities and I am writing to formally report an advers...
{"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 3 weeks ago for macrophage activation syndrome who developed progressive dysphagia, odynophagia, and sev...
SUBJECT: Reaction to Product A with past Product B use and Product A medical query 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 event. The...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 27 year old male patient started on Product A 3 weeks ago for gout prophylaxis who developed severe hyperglycaemia with fasting glucose 10 mmol/L, HbA...
SUBJECT: Product A adverse event with prior Product B and concurrent Omeprazole report Dear Regional Pharmacovigilance Lead, I am the Consultant Pulmonologist 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 informati...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 65 year old male patient started on Product A 3 weeks ago for fibromyalgia who developed acute necrotising fasciitis with severe pain out of proportion, crepitus on examin...
SUBJECT: Product A reaction with prior Product B therapy and clinical information request Dear Regional Pharmacovigilance Lead, I am the Senior Nurse Practitioner at a multi-site primary care network and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical info...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 50 year old female patient started on Product A 15 weeks ago for Graft-versus-host disease who developed drug-induced vasculitis with palpable purpura...
SUBJECT: Product A suspected with Product B background therapy and dosing query Dear Clinical Safety and Regulatory Affairs, I am writing as the caregiver for my wife Diane Alexander 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 37 year old male patient started on Product A 19 weeks ago for osteoporosis who developed severe abdominal pain, bloody diarrhoea more than 4 episodes...
SUBJECT: Product A adverse event and Product B adverse event with Product A guidance needed Dear Adverse Events Reporting Centre, 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 a s...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 47 year old male patient started on Product A 9 weeks ago for autoimmune hepatitis who developed acute tumour lysis syndrome with hyperuricaemia, hype...
SUBJECT: Product A suspected with Product B past use and dosing information request Dear Clinical Safety and Regulatory Affairs, I am the Consultant Endocrinologist at a mental health trust 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": "96%"}, "Analysis": "The email reports an adverse event a 52 year old female patient started on Product A 19 weeks ago for Graft-versus-host disease who developed syncopal episodes, documented bradycardia wit...
SUBJECT: Product A adverse event with prior Product B and concurrent Atorvastatin report Dear Regional Pharmacovigilance Lead, I am writing as the caregiver for my husband Matthew Keller 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", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 65 year old male patient started on Product A 15 weeks ago for multiple sclerosis relapse prevention who developed severe muscle weakness across both lower limbs, signific...
SUBJECT: Both medications suspected with Product A dosing question Hi, I am the Consultant Pulmonologist at a wound care centre network 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 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 29 year old male patient started on Product A 13 weeks ago for sarcoidosis who developed acute agranulocytosis with absolute neutrophil count 0, quali...
SUBJECT: Reporting a serious reaction to Product A stopped Product B last year also on Metformin To Whom It May Concern, I am the Clinical Pharmacist at a large academic medical centre and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting a medic...
{"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 13 weeks ago for narcolepsy who developed new visual disturbances, blurred vision, and bilateral optic disc swelling on ophth...
SUBJECT: Product A and Product B both suspected with Product A information request Dear Medical and Pharmacovigilance Team, I am writing as the caregiver for my father Douglas Edwards 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 26 year old female patient started on Product A 8 weeks ago for pulmonary arterial hypertension who developed severe depression with suicidal ideation...
SUBJECT: Product A adverse event report with historical Product B and guidance request Dear Global Safety and Medical Affairs Unit, I am writing as the caregiver for my mother Pamela Johnson to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 49 year old male patient started on Product A 13 weeks ago for Graft-versus-host disease who developed new-onset shortness of breath, dry cough, and b...
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 hepatology referral centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information request. I ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 43 year old male patient started on Product A 12 weeks ago for fibromyalgia who developed severe abdominal pain, bloody diarrhoea more than 10 episode...
SUBJECT: Product A adverse event and Product B adverse event with Product A guidance needed Dear Adverse Events Reporting Centre, I am the Clinical Pharmacist at a faith-based hospital system and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 32 year old female patient started on Product A 6 weeks ago for Sweet syndrome who developed progressive peripheral neuropathy affecting both hands an...
SUBJECT: Reaction since starting Product A also on Product B and have a dosing question To Whom It May Concern, I am the Head of Pharmacy Services at a hepatology referral centre and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting a medical inf...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 25 year old male patient started on Product A 7 weeks ago for antiphospholipid syndrome who developed toxic epidermal necrolysis with epidermal detach...
SUBJECT: Product A suspected adverse event with Product B stopped and Metformin unchanged Dear Global Safety and Medical Affairs Unit, I am the Director of Clinical Services at an integrated care system and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medica...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 64 year old female patient started on Product A 11 weeks ago for fibromyalgia who developed acute rhabdomyolysis with severe myalgia, creatine kinase 24299 U/L, and myoglo...
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 70 year old female patient started on Product A 20 weeks ago for chronic graft-versus-host disease who developed toxic epidermal necrolysis with epide...
SUBJECT: Product A reaction with prior Product B therapy and clinical information request Dear Regional Pharmacovigilance Lead, I am the Ward Nurse Manager at a large endocrinology centre and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical information requ...
{"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 4 weeks ago for relapsing polychondritis who developed acute tumour lysis syndrome with hyperuricaemia...
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 Gastroenterologist at a residential care home network managing over 400 elderly residents across 5 facilities and I am writing to formally report an adverse ev...
{"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 20 weeks ago for type 2 diabetes who developed acute colonic perforation with pneumoperitoneum on abdominal radiography, peri...
SUBJECT: Product A and Product B suspected adverse reactions with dosing guidance request Dear Post-Marketing Surveillance and Medical Information Unit, 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...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 69 year old male patient started on Product A 9 weeks ago for chronic graft-versus-host disease who developed severely elevated liver enzymes confirme...
SUBJECT: Product A suspected adverse event with Product B stopped and Ibuprofen unchanged 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 rep...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 34 year old female patient started on Product A 19 weeks ago for restless legs syndrome who developed drug-induced immune thrombocytopenic purpura with platelet count 8 x1...
SUBJECT: Formal notification Product A reaction with historical Product B and medical query Dear Pharmacovigilance and Risk Management Team, I am writing as the caregiver for my husband Emilia Jenkins to report an adverse reaction they experienced with a recently started medication and to request related clinical infor...
{"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 15 weeks ago for systemic sclerosis who developed acute disseminated intravascular coagulation with prol...
SUBJECT: Reaction since starting Product A also on Product B and have a dosing question To Whom It May Concern, 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...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 55 year old male patient started on Product A 17 weeks ago for macrophage activation syndrome who developed acute rhabdomyolysis with severe myalgia, ...
SUBJECT: Suspected Product A adverse event with past Product B and ongoing Metformin 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 event....
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 28 year old female patient started on Product A 19 weeks ago for granulomatosis with polyangiitis who developed severe hyponatraemia with serum sodium 114 mmol/L, confusio...
SUBJECT: Product A and Product B suspected adverse reactions with dosing guidance request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Pharmacy Operations Manager at a private cardiology practice group and I am submitting this adverse event report on behalf of a patient who presented to our p...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 54 year old female patient started on Product A 18 weeks ago for type 2 diabetes who developed acute confusion, fever to 39, qualifying as an Adverse ...
SUBJECT: Adverse event report Product A and Product B dual suspect with Product A query Dear Medical Affairs Division, I am writing as the caregiver for my sister Anna Flores to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 73 year old male patient started on Product A 11 weeks ago for ankylosing spondylitis who developed severe headache, visual field defects, and magneti...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information 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 wish ...
{"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 4 weeks ago for polymyositis who developed drug-induced Sweet syndrome with fever, neutrophilia, and t...
SUBJECT: Dual adverse reaction to Product A and Product B with Product A medical query To Whom It May Concern, I am the Consultant Rheumatologist at a rural district hospital 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 s...
{"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 3 weeks ago for Behçet disease who developed acute generalised exanthematous pustulosis with sterile pus...
SUBJECT: Product A adverse event and Product B adverse event with Product A guidance needed Dear Adverse Events Reporting Centre, I am the Ward Nurse Manager at a large endocrinology centre and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical information re...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 62 year old female patient started on Product A 12 weeks ago for inflammatory bowel disease who developed acute necrotising fasciitis with severe pain...
SUBJECT: Product A and Product B suspected adverse reactions with dosing guidance request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Consultant Pulmonologist at a corporate occupational health provider and I am writing to formally report an adverse event involving a patient under my care an...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 84 year old female patient started on Product A 12 weeks ago for juvenile idiopathic arthritis who developed severe arthralgia involving multiple join...
SUBJECT: Product A reaction report with Product B previously used and Product A dose question Dear Sir or Madam, I am the Consultant Haematologist 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. ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 60 year old female patient started on Product A 11 weeks ago for mixed connective tissue disease who developed progressive scleroderma-like skin chang...
SUBJECT: Adverse event to Product A after Product B discontinued with medical query Dear Corporate Drug Safety and Medical Information Department, I am the Senior Nurse Practitioner at a rheumatology clinic group and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 81 year old male patient started on Product A 3 weeks ago for IgA nephropathy who developed acute QT prolongation with corrected QT interval 596 ms, t...
SUBJECT: Product A adverse event report with Product B maintained 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 5 weeks ago for Parkinson disease who developed new-onset seizures with altered consciousness, tongue bi...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information 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 wish ...
{"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 17 weeks ago for narcolepsy who developed a severe generalized maculopapular rash covering more than 38%...
SUBJECT: Product A and Product B suspected adverse reactions with dosing guidance request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Clinical Pharmacist at a specialist dermatology centre and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy serv...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 84 year old female patient started on Product A 19 weeks ago for relapsing polychondritis who developed drug-induced Sweet syndrome with fever, neutro...
SUBJECT: Formal report both Product A and Product B suspect with Product A dose question Dear Patient Safety and Medical Information Team, I am the Consultant Neurologist at an immunology and allergy clinic 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": "97%"}, "Analysis": "The email reports an adverse event a 33 year old male patient started on Product A 3 weeks ago for narcolepsy who developed severe photosensitivity with blistering sunburn-like reaction o...
SUBJECT: Reaction to Product A with past Product B use and Product A medical query Dear Drug Safety Department, I am the Senior Nurse Practitioner at a wound care centre network and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical information request. I wi...
{"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 18 weeks ago for hypothyroidism who developed acute confusion, fever to 40, qualifying as an Adverse E...
SUBJECT: Product A suspect with Product B historical medication and Ibuprofen ongoing Good morning, I am writing as the caregiver for my brother Samuel Chen to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report an adverse event. ...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 61 year old male patient started on Product A 13 weeks ago for primary biliary cholangitis who developed new-onset shortness of breath, dry cough, and bilateral pulmonary ...
SUBJECT: Side effects on Product A with Product B ongoing and Product A information request Dear Drug Safety Department, I am writing as the caregiver for my brother Ralph Warren to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to rep...
{"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 15 weeks ago for ankylosing spondylitis who developed severe arthralgia involving multiple joints with...
SUBJECT: Product A adverse event with historical Product B and Product A information request Dear Medical and Pharmacovigilance 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 wish to report...
{"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 15 weeks ago for granulomatosis with polyangiitis who developed acute angle-closure glaucoma with seve...
SUBJECT: Product A and Product B both implicated with Product A clinical query Dear Clinical Safety and Regulatory Affairs, I am the Attending Physician at a specialist neurology centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information req...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 82 year old female patient started on Product A 11 weeks ago for Parkinson disease who developed severe thrombocytopenia with platelet count 20 x10^9/...
SUBJECT: Formal report involving Product A with historical Product B and background Amoxicillin Dear Corporate Drug Safety and Medical Information 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...
{"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 2 weeks ago for dermatomyositis who developed acute psychosis with paranoid delusions, auditory hallucinations, and aggress...
SUBJECT: Product A and Product B reaction report with clinical information request Dear Global Safety and Medical Affairs Unit, I am the Chief of Medicine at a pathology and diagnostics consortium and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical info...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 79 year old male patient started on Product A 18 weeks ago for acute graft-versus-host disease who developed new visual disturbances, blurred vision, ...
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 48 year old female patient started on Product A 20 weeks ago for autoimmune hepatitis who developed acute kidney injury with serum creatinine rising f...
SUBJECT: Adverse event to Product A after Product B discontinued with medical query Dear Corporate Drug Safety and Medical Information 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 w...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 51 year old male patient started on Product A 11 weeks ago for systemic sclerosis who developed a severe generalized maculopapular rash covering more ...
SUBJECT: Formal notification Product A reaction with historical Product B and medical query Dear Pharmacovigilance and Risk Management 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 ...
{"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 9 weeks ago for granulomatosis with polyangiitis who developed progressive demyelinating polyneuropathy ...
SUBJECT: Product A reaction with historical Product B and concomitant Methotrexate formal notification Dear Patient Safety and Medical Information Team, I am the Consultant Cardiologist at a geriatric medicine consortium and I am writing to formally report an adverse event involving a patient under my care and to reque...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 48 year old female patient started on Product A 18 weeks ago for pulmonary arterial hypertension who developed progressive multifocal leukoencephalopathy with subacute foc...
SUBJECT: Dual adverse reaction to Product A and Product B with Product A medical query To Whom It May Concern, I am writing as the caregiver for my husband Diana Smith to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to report a serio...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 70 year old female patient started on Product A 6 weeks ago for restless legs syndrome who developed acute rhabdomyolysis with severe myalgia, creatin...
SUBJECT: Adverse event report involving Product A with Product B past use and Omeprazole current use Dear Adverse Events Reporting Centre, 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 r...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 62 year old female patient started on Product A 17 weeks ago for axial spondyloarthritis who developed profound fatigue, pallor, and symptomatic anaemia with haemoglobin o...
SUBJECT: Adverse event Product A suspect with historical Product B and Product A query Hi, I am the Consultant Pulmonologist at a rheumatology 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 an adverse event. The ...
{"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 9 weeks ago for mixed connective tissue disease who developed drug-induced vasculitis with palpable purp...
SUBJECT: Side effects on Product A and a dosing question previously on Product B To Whom It May Concern, I am the Consultant Nephrologist 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 to...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 25 year old male patient started on Product A 5 weeks ago for fibromyalgia who developed drug-induced haemolytic anaemia with haemoglobin 7, qualifyin...
SUBJECT: Product A and Product B both implicated with Product A clinical query Dear Clinical Safety and Regulatory Affairs, 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 a serious...
{"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 6 weeks ago for chronic graft-versus-host disease who developed drug-induced haemolytic anaemia with hae...
SUBJECT: Product A suspected with Product B background therapy and dosing query Dear Clinical Safety and Regulatory Affairs, I am writing as the caregiver for my sister Amy Jimenez to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish to r...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 82 year old female patient started on Product A 13 weeks ago for relapsing polychondritis who developed new-onset shortness of breath, dry cough, and ...
SUBJECT: Product A and Product B suspected adverse reactions with dosing guidance request Dear Post-Marketing Surveillance and Medical Information Unit, I am the Clinical Pharmacy Director at a metropolitan ambulance service medical liaison office and I am submitting this adverse event report on behalf of a patient who...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 69 year old male patient started on Product A 2 weeks ago for IgA nephropathy who developed progressive scleroderma-like skin changes with Raynaud phe...
SUBJECT: Adverse event Product A suspect Product B concomitant with Product A query Hi, I am the Consultant Gastroenterologist 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 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 44 year old female patient started on Product A 20 weeks ago for Behçet disease who developed drug-induced vasculitis with palpable purpura, renal inv...
SUBJECT: Product A adverse event and Product B adverse event with Product A guidance needed Dear Adverse Events Reporting Centre, I am the Clinical Pharmacist at a faith-based hospital system and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submitting ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 47 year old male patient started on Product A 2 weeks ago for plaque psoriasis who developed progressive dyspnoea, orthopnoea, and bilateral pleural e...
SUBJECT: Adverse event report involving Product A with Product B past use and Omeprazole current use Dear Adverse Events Reporting Centre, I am the Consultant Nephrologist 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 in...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 47 year old male patient started on Product A 7 weeks ago for pulmonary arterial hypertension who developed progressive demyelinating polyneuropathy with ascending weaknes...
SUBJECT: Product A suspected with Product B historical and Product A clinical guidance sought 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 adver...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 73 year old male patient started on Product A 17 weeks ago for chronic obstructive pulmonary disease who developed drug-induced minimal change disease...
SUBJECT: Product A adverse event with Product B concomitant and Product A medical query Dear Medical and Pharmacovigilance Team, I am the Consultant Nephrologist 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 information. ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 26 year old female patient started on Product A 4 weeks ago for multiple sclerosis relapse prevention who developed severe depression with suicidal id...
SUBJECT: Formal notification Product A reaction with historical Product B and medical query Dear Pharmacovigilance and Risk Management 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 ...
{"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 12 weeks ago for interstitial lung disease who developed severe depression with suicidal ideation, insom...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information Team, I am the Senior Nurse Practitioner at a university hospital department and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a...
{"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 11 weeks ago for gout prophylaxis who developed new-onset seizures with altered consciousness, tongue ...
SUBJECT: Formal report Product A adverse event with concomitant Product B and Product A query Good morning, I am the Clinical Pharmacist at a childrens hospital outpatient 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...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 31 year old male patient started on Product A 12 weeks ago for glaucoma who developed acute posterior reversible encephalopathy syndrome with seizures...
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query Dear Patient Safety and Medical Information Team, I am the Pharmacy Operations Manager at a specialist dermatology centre and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy servic...
{"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 18 weeks ago for juvenile idiopathic arthritis who developed progressive dysphagia, odynophagia, and sev...
SUBJECT: Product A adverse event with historical Product B and concomitant Atorvastatin Dear Medical and Pharmacovigilance Team, I am the Clinical Nurse Specialist at a womens health clinic group and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical informat...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 26 year old female patient started on Product A 18 weeks ago for hypertension who developed acute angle-closure glaucoma with severe ocular pain, blurred vision, and intra...
SUBJECT: Formal report both Product A and Product B suspect with Product A dose question Dear Patient Safety and Medical Information Team, I am the Consultant Nephrologist at a residential care home network managing over 400 elderly residents across 5 facilities and I am writing to formally report an adverse event invo...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 63 year old male patient started on Product A 16 weeks ago for hypertension who developed drug-induced lupus erythematosus with positive antinuclear a...
SUBJECT: Product A and Product B both suspected with Product A information request Dear Medical and Pharmacovigilance Team, I am the Ward Nurse Manager at a cancer centre network and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical information request. I w...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 71 year old male patient started on Product A 17 weeks ago for restless legs syndrome who developed acute necrotising fasciitis with severe pain out o...
SUBJECT: Formal notification Product A reaction with concomitant Product B and medical query Dear Pharmacovigilance and Risk Management Team, I am the Clinical Pharmacy Director at a pharmaceutical benefit manager and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy service...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 83 year old male patient started on Product A 10 weeks ago for Parkinson disease who developed acute colonic perforation with pneumoperitoneum on abdo...
SUBJECT: Product A and Product B reaction report with clinical information request Dear Global Safety and Medical Affairs Unit, I am writing as the caregiver for my husband Hazel Clark to report an adverse reaction they experienced with a recently started medication and to request related clinical information. I wish ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 79 year old male patient started on Product A 4 weeks ago for interstitial lung disease who developed syncopal episodes, documented bradycardia with h...
SUBJECT: Reaction to Product A with past Product B use and Product A medical query Dear Drug Safety Department, I am the Director of Clinical Services at an immunology and allergy clinic 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": "96%"}, "Analysis": "The email reports an adverse event a 57 year old male patient started on Product A 8 weeks ago for rheumatoid arthritis who developed drug-induced lupus erythematosus with positive antinu...
SUBJECT: Product A and Product B suspected adverse reactions with dosing guidance request Dear Post-Marketing Surveillance and Medical Information Unit, I am writing as the caregiver for my mother Victoria Robinson to report an adverse reaction they experienced with a recently started medication and to request related ...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 84 year old female patient started on Product A 17 weeks ago for asthma maintenance who developed severe photosensitivity with blistering sunburn-like...
SUBJECT: Formal report both Product A and Product B suspect with Product A dose question Dear Patient Safety and Medical Information Team, I am the Consultant Pulmonologist 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 inf...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 63 year old male patient started on Product A 9 weeks ago for Sjögren syndrome who developed a severe generalized maculopapular rash covering more tha...
SUBJECT: Product A suspect with Product B historical medication and Levothyroxine ongoing Good morning, I am the Consultant Dermatologist 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 clinical information. I w...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 76 year old female patient started on Product A 9 weeks ago for type 2 diabetes who developed drug-induced immune thrombocytopenic purpura with platelet count 20 x10^9/L, ...
SUBJECT: Reporting a serious reaction to Product A stopped Product B last year also on Ibuprofen 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 an adverse...
{"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 25 year old male patient started on Product A 19 weeks ago for Sjögren syndrome who developed drug-induced minimal change disease with nephrotic range proteinuria 3 g per ...
SUBJECT: Adverse event to Product A after Product B discontinued with medical query Dear Corporate Drug Safety and Medical Information 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 w...
{"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 51 year old male patient started on Product A 20 weeks ago for heart failure with reduced ejection fraction who developed severe photosensitivity with...