instruction stringlengths 1.72k 2.34k | output stringlengths 697 1.25k |
|---|---|
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 dialysis centre network and I am formally notifying you of an adverse event report requiring pharmacovigilance revi... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 39 year old male patient started on Product A 6 weeks ago for acute graft-versus-host disease who developed acute psychosis with paranoid delusions, auditory hallucination... |
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 Attending Physician at a community health partnership covering 12 clinics and I am formally notifying you of an adverse event report requiring pharmacovigilance... | {"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 18 weeks ago for relapsing polychondritis who developed progressive multifocal leukoencephalopathy wit... |
SUBJECT: Product A adverse event report with historical Product B and guidance request
Dear Global Safety and Medical Affairs 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.
I wish to report a... | {"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 8 weeks ago for epilepsy who developed severe hyponatraemia with serum sodium 105 mmol/L, confusion, and... |
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 Gastroenterologist at a managed care organisation 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 17 weeks ago for asthma maintenance who developed progressive multifocal leukoencephalopathy with suba... |
SUBJECT: Product A suspected reaction with Product B unchanged and Product A dose question
Dear Sir or Madam,
I am the Consultant Dermatologist 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 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 4 weeks ago for restless legs syndrome who developed progressive scleroderma-like skin changes with Ra... |
SUBJECT: Product A and Product B adverse reaction with Product A clinical information request
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 a serious adverse ... | {"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 19 weeks ago for gout prophylaxis who developed acute QT prolongation with corrected QT interval 590 ms,... |
SUBJECT: Product A suspected with Product B past use and dosing information request
Dear Clinical Safety and Regulatory Affairs,
I am the Consultant Neurologist 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 ... | {"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 10 weeks ago for interstitial lung disease who developed drug-induced pneumonitis with dyspnoea, bilat... |
SUBJECT: Product A suspected reaction with Product B unchanged and Product A dose question
Dear Sir or Madam,
I am the Consultant Cardiologist 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 information.
I wish to rep... | {"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 3 weeks ago for Parkinson disease who developed acute QT prolongation with corrected QT interval 515 m... |
SUBJECT: Product A suspected with Product B past use and dosing information request
Dear Clinical Safety and Regulatory Affairs,
I am the Director of Clinical Services at a hepatology referral centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical i... | {"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 4 weeks ago for macrophage activation syndrome who developed drug-induced immune thrombocytopenic purpur... |
SUBJECT: Product A suspected with Product B background therapy and dosing query
Dear Clinical Safety and Regulatory Affairs,
I am the Chief of Medicine 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.... | {"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 18 weeks ago for haemophagocytic lymphohistiocytosis who developed drug-induced pneumonitis with dyspnoe... |
SUBJECT: Product A adverse event with prior Product B and concurrent Amlodipine report
Dear Regional Pharmacovigilance Lead,
I am writing as the caregiver for my wife Nicole Gutierrez 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", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 80 year old female patient started on Product A 18 weeks ago for Graft-versus-host disease who developed new-onset atrial fibrillation with rapid ventricular response, pal... |
SUBJECT: Product A adverse event and Product B adverse event with Product A guidance needed
Dear Adverse Events Reporting Centre,
I am the Consultant Dermatologist at a university hospital department 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": "97%"}, "Analysis": "The email reports an adverse event a 32 year old female patient started on Product A 13 weeks ago for atrial fibrillation who developed acute angle-closure glaucoma with severe ocular pai... |
SUBJECT: Product A adverse event report with historical Product B and guidance request
Dear Global Safety and Medical Affairs Unit,
I am the Consultant Gastroenterologist 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 inf... | {"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 3 weeks ago for axial spondyloarthritis who developed acute rhabdomyolysis with severe myalgia, creatine... |
SUBJECT: Product A reaction with historical Product B and concomitant Amoxicillin formal notification
Dear Patient Safety and Medical Information Team,
I am the Pharmacy Operations Manager at a clinical research site network and I am submitting this adverse event report on behalf of a patient who presented to our pharm... | {"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 4 weeks ago for rheumatoid arthritis who developed acute confusion, fever to 39, qualifying as an Adverse Event with Produc... |
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 Dermatologist 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 32 year old female patient started on Product A 16 weeks ago for restless legs syndrome who developed acute hepatitis with alanine aminotransferase 1507 U/L, bilirubin 37 ... |
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 as the caregiver for my husband Aaliyah Campbell to report an adverse reaction they experienced with a recently started medication and to request related cl... | {"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 6 weeks ago for psoriatic arthritis who developed drug-induced Sweet syndrome with fever, neutrophilia, ... |
SUBJECT: Product A reaction report with Product B discontinued and Omeprazole continued
Hi,
I am the Clinical Nurse Specialist at a dialysis 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 wish to report an advers... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 59 year old male patient started on Product A 10 weeks ago for primary biliary cholangitis who developed acute colonic perforation with pneumoperitoneum on abdominal radio... |
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 27 year old male patient started on Product A 17 weeks ago for focal segmental glomerulosclerosis who developed progressive multifocal leukoencephalop... |
SUBJECT: Suspected Product A reaction with Product B historical 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 wish... | {"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 14 weeks ago for heart failure with reduced ejection fraction who developed drug-induced lupus erythem... |
SUBJECT: Product A side effects with Product B stopped months ago and Product A information
Dear Adverse Events Reporting Centre,
I am the Senior Nurse Practitioner at a group of private outpatient clinics and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinica... | {"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 6 weeks ago for narcolepsy who developed severe depression with suicidal ideation, insomnia, and anhed... |
SUBJECT: Product A reaction with historical Product B and concomitant Amoxicillin formal notification
Dear Patient Safety and Medical Information Team,
I am the Clinical Nurse Specialist at a private cardiology practice group and I am documenting this adverse event report on behalf of a patient under our ward care and ... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 33 year old male patient started on Product A 15 weeks ago for IgA nephropathy who developed a severe generalized maculopapular rash covering more than 48% of body surface... |
SUBJECT: Product A and Product B both implicated with Product A clinical query
Dear Clinical Safety and Regulatory Affairs,
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 52 year old female patient started on Product A 3 weeks ago for glaucoma who developed new visual disturbances, blurred vision, and bilateral optic di... |
SUBJECT: Product A suspected with Product B past use and dosing information request
Dear Clinical Safety and Regulatory Affairs,
I am the Senior Consultant 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 wish... | {"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 8 weeks ago for relapsing polychondritis who developed acute myocarditis with chest pain, elevated tro... |
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 sister Chloe Fisher 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": "97%"}, "Analysis": "The email reports an adverse event a 62 year old female patient started on Product A 5 weeks ago for hypertension who developed severe muscle weakness across both lower limbs, significant... |
SUBJECT: Product A side effects with Product B stopped months ago and Product A information
Dear Adverse Events Reporting Centre,
I am the Consultant Dermatologist at a geriatric medicine consortium 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 47 year old male patient started on Product A 18 weeks ago for axial spondyloarthritis who developed profound fatigue, pallor, and symptomatic anaemia... |
SUBJECT: Suspected adverse events with both Product A and Product B and medical query
Dear Regional Pharmacovigilance Lead,
I am the Consultant Pulmonologist at a pharmaceutical benefit manager 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": "97%"}, "Analysis": "The email reports an adverse event a 35 year old male patient started on Product A 18 weeks ago for hypothyroidism who developed new-onset atrial fibrillation with rapid ventricular respo... |
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 68 year old female patient started on Product A 10 weeks ago for IgA nephropathy who developed progressive bronchiolitis obliterans with dyspnoea, fix... |
SUBJECT: Product A and Product B both implicated with Product A clinical query
Dear Clinical Safety and Regulatory Affairs,
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 clinical informatio... | {"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 8 weeks ago for ulcerative colitis maintenance who developed new-onset shortness of breath, dry cough, a... |
SUBJECT: Suspected Product A adverse event with past Product B and ongoing Levothyroxine
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 adverse ... | {"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 13 weeks ago for an autoimmune skin condition who developed acute generalised exanthematous pustulosis with sterile pustule... |
SUBJECT: Product A reaction with historical Product B and concomitant Lisinopril formal notification
Dear Patient Safety and Medical Information Team,
I am the Attending Physician at a specialist dermatology centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concu... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 78 year old female patient started on Product A 10 weeks ago for systemic lupus erythematosus who developed acute QT prolongation with corrected QT interval 593 ms, torsad... |
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 multi-site primary care network and I am writing to formally report an adverse event involving a patient under my care and to request ... | {"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 2 weeks ago for macrophage activation syndrome who developed drug-induced lupus erythematosus with pos... |
SUBJECT: Side effects on Product A and a dosing question previously on Product B
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 patien... | {"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 7 weeks ago for osteoporosis who developed acute myocarditis with chest pain, elevated troponin 690 ng/L... |
SUBJECT: Reaction to Product A with past Product B use and Product A medical query
Dear Drug Safety Department,
I am the Pharmacy Operations Manager at a corporate occupational health provider 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": "96%"}, "Analysis": "The email reports an adverse event a 42 year old female patient started on Product A 20 weeks ago for Sweet syndrome who developed acute psychosis with paranoid delusions, auditory halluc... |
SUBJECT: Adverse event report Product A and Product B dual suspect with Product A query
Dear Medical Affairs Division,
I am the Consultant Hepatologist 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 ... | {"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 19 weeks ago for dermatomyositis who developed severe hyponatraemia with serum sodium 105 mmol/L, confus... |
SUBJECT: Adverse event report Product A and Product B dual suspect with Product A query
Dear Medical Affairs Division,
I am the Consultant Cardiologist 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 wish to r... | {"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 5 weeks ago for multiple sclerosis relapse prevention who developed toxic epidermal necrolysis with epid... |
SUBJECT: Product A suspected adverse event with Product B stopped and Ibuprofen unchanged
Dear Global Safety and Medical Affairs 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.
I wish to repor... | {"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 9 weeks ago for Crohn disease who developed acute myocarditis with chest pain, elevated troponin 1294 ng/L, and cardiac magne... |
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 12 weeks ago for osteoporosis who developed acute necrotising fasciitis with severe pain out of propor... |
SUBJECT: Serious reaction involving both Product A and Product B and Product A guidance sought
Dear Drug Safety Department,
I am writing as the caregiver for my wife Elizabeth Lane 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": "97%"}, "Analysis": "The email reports an adverse event a 57 year old male patient started on Product A 18 weeks ago for Crohn disease who developed severe hyperglycaemia with fasting glucose 16 mmol/L, HbA1c... |
SUBJECT: Product A side effects with Product B stopped months ago and Product A information
Dear Adverse Events Reporting Centre,
I am the Ward Nurse Manager at a childrens hospital outpatient department and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical ... | {"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 15 weeks ago for asthma maintenance who developed progressive bronchiolitis obliterans with dyspnoea, fi... |
SUBJECT: Formal report involving Product A with historical Product B and background Lisinopril
Dear Corporate Drug Safety and Medical Information Department,
I am the Pharmacy Operations Manager at a group of private outpatient clinics and I am submitting this adverse event report on behalf of a patient who presented t... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 81 year old male patient started on Product A 17 weeks ago for benign prostatic hyperplasia who developed progressive scleroderma-like skin changes with Raynaud phenomenon... |
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 an integrated care system 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... | {"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 9 weeks ago for sarcoidosis who developed drug-induced Sweet syndrome with fever, neutrophilia, and tend... |
SUBJECT: Product A reaction report with Product B discontinued and Atorvastatin continued
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 experie... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 44 year old female patient started on Product A 14 weeks ago for chronic obstructive pulmonary disease who developed acute disseminated intravascular coagulation with prol... |
SUBJECT: Formal report Product A adverse event with historical Product B and Product A query
Good morning,
I am the Consultant Neurologist 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 information.
I wish to report an adverse... | {"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 14 weeks ago for dermatomyositis who developed new-onset shortness of breath, dry cough, and bilateral... |
SUBJECT: Product A reaction with prior Product B therapy and clinical information request
Dear Regional Pharmacovigilance Lead,
I am the Consultant Haematologist at a childrens hospital outpatient department and I am writing to formally report an adverse event involving a patient under my care and to request clinical i... | {"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 3 weeks ago for type 2 diabetes who developed progressive bronchiolitis obliterans with dyspnoea, fixed ... |
SUBJECT: Formal notification Product A reaction with concomitant Product B and medical query
Dear Pharmacovigilance and Risk Management Team,
I am the Consultant Nephrologist 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 ... | {"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 15 weeks ago for plaque psoriasis who developed acute angle-closure glaucoma with severe ocular pain, ... |
SUBJECT: Adverse event Product A suspect with historical Product B and Product A query
Hi,
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 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 59 year old male patient started on Product A 12 weeks ago for rheumatoid arthritis who developed progressive peripheral neuropathy affecting both han... |
SUBJECT: Formal adverse event notification for Product A and Product B with medical information
Dear Pharmacovigilance and Risk Management Team,
I am writing as the caregiver for my elderly aunt Abigail Carpenter to report an adverse reaction they experienced with a recently started medication and to request related cl... | {"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 5 weeks ago for depression who developed drug-induced vasculitis with palpable purpura, renal involvem... |
SUBJECT: Adverse event Product A suspect with historical Product B and Product A query
Hi,
I am writing as the caregiver for my sister Bruce Carter 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. The patie... | {"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 17 weeks ago for lupus nephritis who developed acute tumour lysis syndrome with hyperuricaemia, hyperkal... |
SUBJECT: Product A suspected with Product B background therapy and dosing query
Dear Clinical Safety and Regulatory Affairs,
I am the Consultant Nephrologist 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 52 year old female patient started on Product A 2 weeks ago for primary biliary cholangitis who developed anaphylaxis within 17 minutes of dosing incl... |
SUBJECT: Product A adverse event with prior Product B and concurrent Omeprazole report
Dear Regional Pharmacovigilance Lead,
I am writing as the caregiver for my husband Virginia Ryan 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", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 80 year old female patient started on Product A 13 weeks ago for systemic lupus erythematosus who developed severe depression with suicidal ideation, insomnia, and anhedon... |
SUBJECT: Product A side effects with Product B stopped months ago and Product A information
Dear Adverse Events Reporting Centre,
I am the Pharmacy Operations Manager at a surgical day case unit group and I am submitting this adverse event report on behalf of a patient who presented to our pharmacy services and also su... | {"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 9 weeks ago for autoimmune hepatitis who developed acute disseminated intravascular coagulation with p... |
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 54 year old female patient started on Product A 8 weeks ago for glaucoma who developed progressive sensorineural hearing loss with high-frequency thre... |
SUBJECT: Product A reaction report with Product B previously used and Product A dose question
Dear Sir or Madam,
I am the Medical Director at a respiratory medicine centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information request.
I wish ... | {"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 20 weeks ago for ulcerative colitis maintenance who developed new-onset seizures with altered consciousn... |
SUBJECT: Product A adverse event report with Product B historical and clinical request
Dear Post-Marketing Surveillance and Medical Information Unit,
I am the Consultant Rheumatologist at a rheumatology clinic group and I am writing to formally report an adverse event involving a patient under my care and to request cl... | {"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 7 weeks ago for pulmonary arterial hypertension who developed severely elevated liver enzymes confirmed ... |
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 48 year old female patient started on Product A 13 weeks ago for Crohn disease who developed severe hyperglycaemia with fasting glucose 19 mmol/L, HbA... |
SUBJECT: Suspected adverse events with both Product A and Product B and medical query
Dear Regional Pharmacovigilance Lead,
I am the Chief of Medicine at a rheumatology clinic group and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information request... | {"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 20 weeks ago for chronic obstructive pulmonary disease who developed acute hepatitis with alanine amin... |
SUBJECT: Product A and Product B both suspected with Product A information request
Dear Medical and Pharmacovigilance Team,
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 56 year old female patient started on Product A 14 weeks ago for Behçet disease who developed acute tumour lysis syndrome with hyperuricaemia, hyperka... |
SUBJECT: Product A adverse event with historical Product B and 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 repo... | {"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 17 weeks ago for hypertension who developed acute colonic perforation with pneumoperitoneum on abdomin... |
SUBJECT: Product A adverse event with Product B concomitant and Product A medical query
Dear Medical and Pharmacovigilance Team,
I am the Consultant Neurologist 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 41 year old male patient started on Product A 9 weeks ago for chronic pain who developed progressive bronchiolitis obliterans with dyspnoea, fixed obs... |
SUBJECT: Formal notification Product A reaction with concomitant Product B and medical query
Dear Pharmacovigilance and Risk Management Team,
I am the Clinical Nurse Specialist at a corporate occupational health provider 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 83 year old male patient started on Product A 9 weeks ago for atrial fibrillation who developed acute agranulocytosis with absolute neutrophil count 0... |
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 60 year old female patient started on Product A 5 weeks ago for autoimmune hepatitis who developed a severe generalized maculopapular rash covering mo... |
SUBJECT: Reporting a serious reaction to Product A stopped Product B last year also on Metformin
To Whom It May Concern,
I am the Consultant Haematologist 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 wis... | {"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 14 weeks ago for inflammatory bowel disease who developed drug-induced immune thrombocytopenic purpura with platelet count 5 ... |
SUBJECT: Product A and Product B both suspected with Product A information request
Dear Medical and Pharmacovigilance Team,
I am the Consultant Rheumatologist 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... | {"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 20 weeks ago for asthma maintenance who developed progressive bronchiolitis obliterans with dyspnoea, ... |
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 54 year old female patient started on Product A 17 weeks ago for systemic sclerosis who developed progressive restrictive cardiomyopathy with diastoli... |
SUBJECT: Dual suspect drug reaction Product A and Product B with Product A medical query
Good morning,
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 wish to report a... | {"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 8 weeks ago for diabetic neuropathy who developed new visual disturbances, blurred vision, and bilateral... |
SUBJECT: Formal report Product A adverse event with historical Product B and Product A query
Good morning,
I am the Consultant Neurologist at a university hospital department 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 ... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 61 year old male patient started on Product A 20 weeks ago for Parkinson disease who developed severe hyponatraemia with serum sodium 117 mmol/L, conf... |
SUBJECT: Product A reaction with historical Product B and concomitant Methotrexate formal notification
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 produ... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 78 year old female patient started on Product A 17 weeks ago for Crohn disease who developed severe arthralgia involving multiple joints with morning stiffness exceeding 2... |
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 14 weeks ago for restless legs syndrome who developed new-onset seizures with altered consciousness, ton... |
SUBJECT: Reaction to Product A with past Product B use and Product A medical query
Dear Drug Safety Department,
I am the Consultant Gastroenterologist 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.
I wish to repor... | {"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 19 weeks ago for hypertension who developed severe arthralgia involving multiple joints with morning sti... |
SUBJECT: Dual suspect drug reaction Product A and Product B with Product A medical query
Good morning,
I am writing as the caregiver for my husband Sharon Mitchell to report an adverse reaction they experienced with a recently started medication and to request related clinical information.
I wish to report a serious a... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 46 year old female patient started on Product A 17 weeks ago for autoimmune hepatitis who developed acute generalised exanthematous pustulosis with st... |
SUBJECT: Formal report Product A adverse event with concomitant Product B and Product A query
Good morning,
I am the Medical Director at a large academic medical centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information request.
I wish to ... | {"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 8 weeks ago for myasthenia gravis who developed severe thrombocytopenia with platelet count 14 x10^9/L... |
SUBJECT: Product A reaction report with concomitant Product B and Product A guidance sought
Dear Medical Affairs Division,
I am the Attending Physician at a specialist dermatology 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": "96%"}, "Analysis": "The email reports an adverse event a 43 year old male patient started on Product A 4 weeks ago for systemic lupus erythematosus who developed severe abdominal pain, bloody diarrhoea more ... |
SUBJECT: Product A reaction report with concomitant Product B and Product A 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 adverse... | {"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 17 weeks ago for osteoporosis who developed new-onset shortness of breath, dry cough, and bilateral pu... |
SUBJECT: Adverse event Product A suspect Product B concomitant with Product A query
Hi,
I am the Medical Director at a university hospital department 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 adverse e... | {"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 2 weeks ago for a chronic inflammatory condition who developed progressive demyelinating polyneuropath... |
SUBJECT: Product A suspected with Product B past use and dosing information request
Dear Clinical Safety and Regulatory Affairs,
I am writing as the caregiver for my husband Gavin Lawson 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 52 year old female patient started on Product A 13 weeks ago for systemic sclerosis who developed severe headache, visual field defects, and magnetic ... |
SUBJECT: Product A and Product B both implicated with Product A clinical query
Dear Clinical Safety and Regulatory Affairs,
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 67 year old male patient started on Product A 20 weeks ago for granulomatosis with polyangiitis who developed drug-induced pneumonitis with dyspnoea, ... |
SUBJECT: Product A adverse event with prior Product B and concurrent Amlodipine report
Dear Regional Pharmacovigilance Lead,
I am the Consultant Pulmonologist 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 50 year old female patient started on Product A 19 weeks ago for focal segmental glomerulosclerosis who developed acute tumour lysis syndrome with hyperuricaemia, hyperkal... |
SUBJECT: Product A and Product B adverse reaction with Product A clinical information request
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 a serious adverse ev... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 60 year old female patient started on Product A 4 weeks ago for vasculitis who developed severely elevated liver enzymes confirmed on blood testing, p... |
SUBJECT: Product A suspected with Product B historical and Product A clinical guidance sought
Dear Medical Affairs Division,
I am the Clinical Pharmacist 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 submitting a... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "96%"}, "Analysis": "The email reports an adverse event a 43 year old male patient started on Product A 19 weeks ago for membranous nephropathy who developed severe headache, visual field defects, and magneti... |
SUBJECT: Suspected reaction to Product A with Product B historical and Levothyroxine maintained
Dear Clinical Safety and Regulatory Affairs,
I am writing as the caregiver for my elderly aunt Michael West to report an adverse reaction they experienced with a recently started medication and to request related clinical in... | {"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 11 weeks ago for a chronic inflammatory condition who developed severe thrombocytopenia with platelet count 11 x10^9/L and mu... |
SUBJECT: Product A reaction with historical Product B and concomitant Methotrexate formal notification
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 produ... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 33 year old male patient started on Product A 8 weeks ago for restless legs syndrome who developed progressive sensorineural hearing loss with high-frequency threshold ele... |
SUBJECT: Product A adverse event with historical Product B and concomitant Amlodipine
Dear Medical and Pharmacovigilance Team,
I am writing as the caregiver for my elderly uncle Kenneth Ferguson to report an adverse reaction they experienced with a recently started medication and to request related clinical information... | {"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 12 weeks ago for systemic sclerosis who developed progressive demyelinating polyneuropathy with ascending weakness, areflex... |
SUBJECT: Formal report involving Product A with historical Product B and background Amoxicillin
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 81 year old male patient started on Product A 10 weeks ago for Graft-versus-host disease who developed new-onset seizures with altered consciousness, tongue biting, and po... |
SUBJECT: Product A adverse event and Product B adverse event with Product A guidance needed
Dear Adverse Events Reporting Centre,
I am the Consultant Hepatologist at a residential care home network managing over 400 elderly residents across 5 facilities and I am writing to formally report an adverse event involving a p... | {"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 10 weeks ago for myasthenia gravis who developed drug-induced vasculitis with palpable purpura, renal in... |
SUBJECT: Product A suspected adverse event with Product B stopped and Levothyroxine unchanged
Dear Global Safety and Medical Affairs 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.
I wish to r... | {"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 14 weeks ago for benign prostatic hyperplasia who developed severe hyponatraemia with serum sodium 111 mmol/L, confusion, and... |
SUBJECT: Formal notification Product A reaction with historical Product B and medical query
Dear Pharmacovigilance and Risk Management Team,
I am the Chief of Medicine at a multi-site primary care network 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": "96%"}, "Analysis": "The email reports an adverse event a 68 year old female patient started on Product A 19 weeks ago for ankylosing spondylitis who developed new-onset atrial fibrillation with rapid ventric... |
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 Pulmonologist 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": "97%"}, "Analysis": "The email reports an adverse event a 81 year old male patient started on Product A 19 weeks ago for Parkinson disease who developed a severe generalized maculopapular rash covering more t... |
SUBJECT: Product A suspected with Product B past use and dosing information request
Dear Clinical Safety and Regulatory Affairs,
I am the Attending Physician at a hepatology referral centre and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information... | {"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 12 weeks ago for Sjögren syndrome who developed new visual disturbances, blurred vision, and bilateral o... |
SUBJECT: Suspected Product A adverse event with past Product B and ongoing Metformin
Dear Medical Affairs Division,
I am the Head of Pharmacy Services at a surgical day case unit group 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 43 year old male patient started on Product A 10 weeks ago for Parkinson disease who developed drug-induced minimal change disease with nephrotic range proteinuria 5 g per... |
SUBJECT: Pharmacovigilance report Product A with Product B historical and Lisinopril concomitant
Dear Post-Marketing Surveillance and Medical Information Unit,
I am the Consultant Neurologist at a pain management clinic group and I am writing to formally report an adverse event involving a patient under my care and to ... | {"Classification_of_request": {"Classification": "Adverse Event", "Confidence_percentage": "98%"}, "Analysis": "The email reports an adverse event a 84 year old female patient started on Product A 3 weeks ago for inflammatory bowel disease who developed progressive sensorineural hearing loss with high-frequency thresho... |
SUBJECT: Formal report Product A adverse event with historical Product B and Product A query
Good morning,
I am writing as the caregiver for my elderly uncle Naomi Greene 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 61 year old male patient started on Product A 7 weeks ago for autoimmune hepatitis who developed severe headache, visual field defects, and magnetic r... |
SUBJECT: Product A adverse event report with Product B concomitant and dose guidance request
Dear Global Safety and Medical Affairs Unit,
I am the Ward Nurse Manager at a private cardiology practice group and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical... | {"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 13 weeks ago for dermatomyositis who developed toxic epidermal necrolysis with epidermal detachment co... |
SUBJECT: Suspected Product A reaction with concomitant Product B and Product A medical query
Dear Patient Safety and Medical Information Team,
I am writing as the caregiver for my mother Mason Meyer to report an adverse reaction they experienced with a recently started medication and to request related clinical informa... | {"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 8 weeks ago for sarcoidosis who developed acute kidney injury with serum creatinine rising from baseline... |
SUBJECT: Suspected Product A reaction with Product B historical 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 t... | {"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 4 weeks ago for chronic migraine prophylaxis who developed acute QT prolongation with corrected QT int... |
SUBJECT: Product A and Product B adverse reaction with Product A clinical information request
Dear Sir or Madam,
I am the Medical Director at a multi-site primary care network and I am formally notifying you of an adverse event report requiring pharmacovigilance review and a concurrent medical information request.
I w... | {"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 2 weeks ago for mixed connective tissue disease who developed progressive dysphagia, odynophagia, and se... |
SUBJECT: Product A and Product B adverse reaction with Product A clinical information request
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 a serious adverse ... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 45 year old male patient started on Product A 13 weeks ago for antiphospholipid syndrome who developed acute confusion, fever to 38, qualifying as an ... |
SUBJECT: Product A adverse event report with Product B concomitant and dose guidance request
Dear Global Safety and Medical Affairs Unit,
I am the Clinical Pharmacy Director 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 a... | {"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 14 weeks ago for Sweet syndrome who developed acute posterior reversible encephalopathy syndrome with ... |
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 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 info... | {"Classification_of_request": {"Classification": "Adverse Event, Medical Information", "Confidence_percentage": "97%"}, "Analysis": "The email reports an adverse event a 65 year old male patient started on Product A 12 weeks ago for Sjögren syndrome who developed progressive dyspnoea, orthopnoea, and bilateral pleural ... |
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 70 year old female patient started on Product A 19 weeks ago for axial spondyloarthritis who developed drug-induced immune thrombocytopenic purpura wi... |
SUBJECT: Dual suspect drug reaction Product A and Product B with Product A medical query
Good morning,
I am the Clinical Nurse Specialist at a Veterans Affairs medical centre and I am documenting this adverse event report on behalf of a patient under our ward care and forwarding a clinical information request.
I wish ... | {"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 18 weeks ago for myasthenia gravis who developed acute myocarditis with chest pain, elevated troponin ... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.