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Index of reports
> Cases resulting in disability (3)
> Cases with Toxic Epidermal Necrolysis (3)
Below is the selection of adverse event reports related to Ethyol (Amifostine) that includes cases resulting in disability where reactions include toxic epidermal necrolysis.
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a individual with unspecified qualification from France on 2007-06-07
Patient: 68 year old male
Adverse reactions / side effects: Ischaemia, Serratia Infection, Corneal Perforation, Radiation Skin Injury, Pyrexia, Bronchial Obstruction, Erythema, Fall, Somnolence, Haemodynamic Instability, Multi-Organ Failure, Malaise, Poor Peripheral Circulation, Hypoxia, Pleural Effusion, Histiocytosis Haematophagic, Dysphagia, Hypothermia, Hypotension, Toxic Epidermal Necrolysis, Respiratory Distress, Mucosal Inflammation, Agranulocytosis, Renal Failure, Respiratory Failure, Staphylococcal Infection, Heart Rate Increased, Sepsis, Disturbance in Attention, Dermatitis Exfoliative, Leukopenia
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Ethyol
Dosage: 340 mg, 3 in 1 wk, intravenous (not otherwise specified)
Indication: Prophylaxis
Start date: 2006-09-28
End date: 2006-11-06
Ethyol
Dosage: 340 mg, 3 in 1 wk, intravenous (not otherwise specified)
Indication: Radiotherapy
Start date: 2006-09-28
End date: 2006-11-06
Ciprofloxacin
Dosage: oral
Administration route: Oral
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Augmentin '125'
Dosage: intravenous (not otherwise specified)
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Fluconazole
Dosage: intravenous (not otherwise specified)
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Acetaminophen
Dosage: intravenous (not otherwise specified)
Start date: 2006-11-06
End date: 2006-11-07
Primperan TAB
Dosage: intravenous (not otherwise specified)
Indication: Nausea
Start date: 2006-11-06
End date: 2006-11-06
Primperan TAB
Dosage: intravenous (not otherwise specified)
Indication: Vomiting
Start date: 2006-11-06
End date: 2006-11-06
Other drugs received by patient: Citalopram Hydrobromide; Lorazepam; Zaldiar (Paracetamol, Tramadol Hydrochloride); Acetaminophen; Radiation Therapy
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a individual with unspecified qualification from France on 2007-05-14
Patient: 68 year old male
Adverse reactions / side effects: Serratia Infection, Ulcerative Keratitis, Bronchial Obstruction, Tympanic Membrane Perforation, Adhesion, Post Procedural Infection, Histiocytosis Haematophagic, Dysphagia, Hypotension, Toxic Epidermal Necrolysis, General Physical Health Deterioration, Respiratory Distress, Staphylococcal Infection, Depressed Level of Consciousness, Nervous System Disorder, Otitis Media, Dermatitis Exfoliative, Keratitis, Transplant, Ischaemia, Head Injury, Corneal Perforation, Symblepharon, Somnolence, Fall, Multi-Organ Failure, Eyelid Disorder, Pleural Effusion, Pathogen Resistance, Catheter Site Infection, Hernia, Mucosal Inflammation, Agranulocytosis, Renal Failure, Iris Disorder, Respiratory Failure, Heart Rate Increased, Sepsis, Peripheral Circulatory Failure, Leukopenia, Shock, Infusion Related Reaction
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Ethyol
Dosage: 340 mg, 3 in 1 wk, intravenous
Indication: Prophylaxis
Start date: 2006-09-28
End date: 2006-11-06
Ethyol
Dosage: 340 mg, 3 in 1 wk, intravenous
Indication: Radiotherapy
Start date: 2006-09-28
End date: 2006-11-06
Ciprofloxacin
Dosage: oral
Administration route: Oral
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Augmentin '125'
Dosage: intravenous
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Fluconazole
Dosage: intravenous
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Perfalgan (Paracetamol)
Dosage: intravenous
Start date: 2006-11-06
End date: 2006-11-07
Primperan TAB
Dosage: intravenous
Indication: Nausea
Start date: 2006-11-06
End date: 2006-11-06
Primperan TAB
Dosage: intravenous
Indication: Vomiting
Start date: 2006-11-06
End date: 2006-11-06
Other drugs received by patient: Citalopram Hydrobromide; Lorazepam; Zaldiar (Paracetamol, Tramadol Hydrochloride); Acetaminophen; Radiation Therapy
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a physician from France on 2007-05-01
Patient: 68 year old male
Adverse reactions / side effects: Skin Exfoliation, Conjunctival Oedema, Symblepharon, Toxic Epidermal Necrolysis, Erythema, Eye Infection, Haemodynamic Instability, Multi-Organ Failure, Renal Failure, Agranulocytosis, Respiratory Failure, Nervous System Disorder, Eye Disorder, Keratitis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Ciprofloxacin HCL
Dosage: total daily dose: 1 g unit dose: 500 mg
Administration route: Oral
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Augmentin '125'
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Triflucan
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Ethyol
Indication: Unevaluable Event
Start date: 2006-09-28
End date: 2006-11-06
Perfalgan
Indication: Unevaluable Event
Start date: 2006-11-06
End date: 2006-11-07
Primperan INJ
Dosage: total daily dose: 60 mg unit dose: 10 mg
Indication: Nausea
Start date: 2006-11-06
End date: 2006-11-06
Other drugs received by patient: Seropram; Temesta; Acetaminophen and Tramadol HCL; Acetaminophen
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