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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... |
SUBJECT: Dual suspect drug reaction Product A and Product B with Product A medical query
Good morning,
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 adverse event where ... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 76 year old female patient started on Product A 4 weeks ago for acute graft-versus-host disease who developed severe hyponatraemia with serum sodium 1... |
SUBJECT: Formal report Product A adverse event with concomitant Product B and Product A query
Good morning,
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 pat... | {"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 6 weeks ago for an autoimmune skin condition who developed severe abdominal pain, bloody diarrhoea mor... |
SUBJECT: Suspected adverse events with both Product A and Product B and medical query
Dear Regional Pharmacovigilance Lead,
I am the Consultant Hepatologist 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 w... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 35 year old male patient started on Product A 11 weeks ago for an autoimmune skin condition who developed progressive demyelinating polyneuropathy wit... |
SUBJECT: Suspected Product A reaction with Product B historical and Product A medical query
Dear Patient Safety and Medical Information Team,
I am the Consultant Haematologist 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 clinic... | {"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 20 weeks ago for axial spondyloarthritis who developed severely elevated liver enzymes confirmed on bl... |
SUBJECT: Product A and Product B both suspected with Product A information request
Dear Medical and Pharmacovigilance Team,
I am the Clinical Pharmacy Director at a tertiary referral hospital 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 71 year old male patient started on Product A 10 weeks ago for chronic pain who developed severe muscle weakness across both lower limbs, significant ... |
SUBJECT: Product A suspected adverse event with Product B stopped and Metformin unchanged
Dear Global Safety and Medical Affairs Unit,
I am the Chief of Medicine at a private cardiology practice group and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical ... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 79 year old male patient started on Product A 2 weeks ago for systemic lupus erythematosus who developed drug-induced haemolytic anaemia with haemoglobin 5, qualifying as ... |
SUBJECT: Serious reaction involving both Product A and Product B and Product A guidance sought
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 a serio... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 72 year old female patient started on Product A 7 weeks ago for mixed connective tissue disease who developed progressive sensorineural hearing loss w... |
SUBJECT: Suspected reaction to Product A with Product B historical and Metformin maintained
Dear Clinical Safety and Regulatory Affairs,
I am the Consultant Cardiologist 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.
... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 67 year old male patient started on Product A 18 weeks ago for multiple sclerosis relapse prevention who developed acute generalised exanthematous pustulosis with sterile ... |
SUBJECT: Dual suspect drug reaction Product A and Product B with Product A medical query
Good morning,
I am the Attending Physician at a chain of retail pharmacies and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information request.
I wish to repor... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 31 year old male patient started on Product A 9 weeks ago for psoriatic arthritis who developed drug-induced immune thrombocytopenic purpura with plat... |
SUBJECT: Formal report involving Product A with historical Product B and background Lisinopril
Dear Corporate Drug Safety and Medical Information Department,
I am the Medical Director at a home healthcare nursing agency and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a ... | {"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 8 weeks ago for heart failure with reduced ejection fraction who developed severe arthralgia involving multiple joints with... |
SUBJECT: Product A adverse event report with historical Product B and guidance request
Dear Global Safety and Medical Affairs Unit,
I am the Consultant Endocrinologist 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 informatio... | {"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 20 weeks ago for type 2 diabetes who developed acute myocarditis with chest pain, elevated troponin 36... |
SUBJECT: Product A side effects with Product B stopped months ago and Product A information
Dear Adverse Events Reporting Centre,
I am the Consultant Pulmonologist at a private cardiology practice group and I am writing to formally report an adverse event involving a patient under my care and to request clinical inform... | {"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 5 weeks ago for ulcerative colitis maintenance who developed acute tumour lysis syndrome with hyperurica... |
SUBJECT: Adverse event to Product A after Product B discontinued with medical query
Dear Corporate Drug Safety and Medical Information Department,
I am the Attending Physician at a respiratory medicine centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent ... | {"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 13 weeks ago for acute graft-versus-host disease who developed severe arthralgia involving multiple jo... |
SUBJECT: Adverse event to Product A while on Product B with medical information request
Dear Corporate Drug Safety and Medical Information Department,
I am the Ward Nurse Manager at a gastroenterology clinic partnership and I am documenting this adverse event report on behalf of a patient under our ward care and forwar... | {"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 20 weeks ago for inflammatory bowel disease who developed progressive dysphagia, odynophagia, and seve... |
SUBJECT: Product A suspected reaction with Product B unchanged and Product A dose question
Dear Sir or Madam,
I am the Consultant Gastroenterologist 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, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 60 year old female patient started on Product A 5 weeks ago for vasculitis who developed acute confusion, fever to 38, qualifying as an Adverse Event ... |
SUBJECT: Product A side effects with ongoing Product B and Product A clinical information
Dear Adverse Events Reporting Centre,
I am the Consultant Pulmonologist 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 information.
I... | {"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 18 weeks ago for Crohn disease who developed new-onset atrial fibrillation with rapid ventricular resp... |
SUBJECT: Side effects on Product A and a dosing question previously on Product B
To Whom It May Concern,
I am the Consultant Haematologist 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.
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 40 year old female patient started on Product A 3 weeks ago for benign prostatic hyperplasia who developed drug-induced immune thrombocytopenic purpur... |
SUBJECT: Product A reaction with concurrent Product B and clinical information query
Dear Regional Pharmacovigilance Lead,
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 65 year old male patient started on Product A 12 weeks ago for interstitial lung disease who developed acute hepatitis with alanine aminotransferase 2... |
SUBJECT: Formal report Product A reaction with Product B historical and Amoxicillin concomitant
Dear Drug Safety Department,
I am the Pharmacy Operations Manager at a rural district hospital 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 57 year old male patient started on Product A 2 weeks ago for an autoimmune skin condition who developed drug-induced lupus erythematosus with positive antinuclear antibod... |
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 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": "96%"}, "Analysis": "The email reports an adverse event a 81 year old male patient started on Product A 16 weeks ago for pulmonary arterial hypertension who developed acute QT prolongation with corrected QT i... |
SUBJECT: Product A adverse event report with Product B completed course and Atorvastatin ongoing
Dear Pharmacovigilance and Risk Management Team,
I am the Senior Nurse Practitioner at a geriatric medicine consortium and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding... | {"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 13 weeks ago for Graft-versus-host disease who developed acute necrotising fasciitis with severe pain out of proportion, crep... |
SUBJECT: Product A adverse event report with historical Product B and guidance request
Dear Global Safety and Medical Affairs Unit,
I am the Clinical Pharmacy Director at a regional hospital trust and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also submit... | {"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 11 weeks ago for inflammatory bowel disease who developed drug-induced pneumonitis with dyspnoea, bilate... |
SUBJECT: Formal notification Product A reaction with concomitant Product B and medical query
Dear Pharmacovigilance and Risk Management Team,
I am the Consultant Endocrinologist at a dialysis centre network 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 53 year old male patient started on Product A 19 weeks ago for asthma maintenance who developed acute tumour lysis syndrome with hyperuricaemia, hyper... |
SUBJECT: Formal report Product A reaction with Product B historical and Methotrexate concomitant
Dear Drug Safety Department,
I am the Consultant Pulmonologist 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.
I... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 42 year old female patient started on Product A 6 weeks ago for interstitial lung disease who developed acute kidney injury with serum creatinine rising from baseline 87 u... |
SUBJECT: Product A side effects with Product B stopped months ago and Product A information
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 an ... | {"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 14 weeks ago for systemic lupus erythematosus who developed progressive dyspnoea, orthopnoea, and bila... |
SUBJECT: Product A adverse event report with Product B concomitant and dose guidance request
Dear Global Safety and Medical Affairs Unit,
I am writing as the caregiver for my sister Ryan Wallace 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 64 year old female patient started on Product A 16 weeks ago for chronic pain who developed drug-induced pneumonitis with dyspnoea, bilateral ground-g... |
SUBJECT: Serious adverse event Product A with historical Product B and concomitant Methotrexate
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. ... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 45 year old male patient started on Product A 11 weeks ago for juvenile idiopathic arthritis who developed progressive restrictive cardiomyopathy with diastolic dysfunctio... |
SUBJECT: Product A adverse event with historical Product B and concomitant Omeprazole
Dear Medical and Pharmacovigilance Team,
I am the Consultant Dermatologist 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 wis... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 56 year old female patient started on Product A 5 weeks ago for narcolepsy who developed recurrent pancreatitis with severe epigastric pain, serum lipase 14x times upper l... |
SUBJECT: Adverse event to Product A while on Product B with medical information request
Dear Corporate Drug Safety and Medical Information Department,
I am the Pharmacy Operations Manager at a home healthcare nursing agency and I am submitting this adverse event report on behalf of a patient who presented to our pharma... | {"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 11 weeks ago for systemic lupus erythematosus who developed severe arthralgia involving multiple joint... |
SUBJECT: Product A adverse event and Product B adverse event with Product A guidance needed
Dear Adverse Events Reporting Centre,
I am writing as the caregiver for my mother Steven Hunt 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 77 year old male patient started on Product A 8 weeks ago for membranous nephropathy who developed new-onset atrial fibrillation with rapid ventricula... |
SUBJECT: Product A suspected with Product B background therapy and dosing query
Dear Clinical Safety and Regulatory Affairs,
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 wi... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 67 year old male patient started on Product A 7 weeks ago for ulcerative colitis maintenance who developed acute generalised exanthematous pustulosis ... |
SUBJECT: Serious reaction involving both Product A and Product B and Product A guidance sought
Dear Drug Safety Department,
I am the Consultant Haematologist at a womens health clinic group 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 57 year old male patient started on Product A 4 weeks ago for benign prostatic hyperplasia who developed drug-induced Sweet syndrome with fever, neutr... |
SUBJECT: Suspected Product A adverse event with past Product B and ongoing Metformin
Dear Medical Affairs Division,
I am writing as the caregiver for my wife Stephanie Graham 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", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 58 year old female patient started on Product A 20 weeks ago for hypothyroidism who developed anaphylaxis within 53 minutes of dosing including urticaria, angioedema, bron... |
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