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Index of reports
> Cases resulting in other serious reactions (20)
Below is the selection of adverse event reports related to Ethyol (Amifostine) that includes cases resulting in other serious reactions.
Adverse event in 49 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-15
Patient: 49 year old male
Adverse reactions / side effects: Pruritus, Rash Maculo-Papular
Suspect drug(s):
Ethyol (Amifostine)
Adverse event in 56 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-11
Patient: 56 year old male, weighing 70.5 kg (155.2 pounds)
Adverse reactions / side effects: Body Temperature Increased, Rash Maculo-Papular
Suspect drug(s):
Ethyol (Amifostine)
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
Adverse event in 63 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-01
Patient: 63 year old male, weighing 121.6 kg (267.4 pounds)
Adverse reactions / side effects: Skin Chapped, Skin Exfoliation, Chills, Erythema, Pruritus Generalised, Malaise, Oedema Peripheral, Oral Mucosa Erosion, Blister, Vomiting, Swelling Face, Rash Generalised, Nausea, Drug Hypersensitivity, Pain of Skin, DRY Skin, Burning Sensation, Anxiety, Arthralgia, Diarrhoea
Suspect drug(s):
Ethyol
Dosage: see image
Indication: Adenocarcinoma
Start date: 2006-11-28
End date: 2006-12-05
Ethyol
Dosage: see image
Indication: Adenocarcinoma
Start date: 2006-12-06
End date: 2006-12-29
Other drugs received by patient: Triamterene and Hydrochlorothiazide (Hydrochlorothiazide, Triamterene); Lorazepam; Acetaminophen and Oxycodone HCL; Allegra; Kytril; Radiation Therapy
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a individual with unspecified qualification from France on 2007-05-01
Patient: 68 year old male
Adverse reactions / side effects: Serratia Infection, Radiation Injury, Ulcerative Keratitis, Corneal Disorder, Haemodynamic Instability, Tympanic Membrane Perforation, Adhesion, Dysphagia, Histiocytosis Haematophagic, Hypothermia, Conjunctival Oedema, Hypotension, Toxic Epidermal Necrolysis, Respiratory Distress, Staphylococcal Infection, Dysphonia, Disturbance in Attention, Dermatitis Exfoliative, Keratitis, Ischaemia, Head Injury, Corneal Perforation, Symblepharon, Fall, Somnolence, Multi-Organ Failure, Pleural Effusion, Ear Infection, Hernia, Blood Culture, Mucosal Inflammation, Renal Failure, Agranulocytosis, Respiratory Failure, Eyelid Function Disorder, Sepsis, Leukopenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Citalopram Hydrobromide; Lorazepam; (Paracetamol, Tramadol Hydrochloride); Acetaminophen; Radiation Therapy
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-30
Patient: 68 year old male
Adverse reactions / side effects: Multi-Organ Failure, Agranulocytosis, Toxic Epidermal Necrolysis, Eye Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Triflucan
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Ciprofloxacin
Dosage: text:1 g
Administration route: Oral
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Augmentin '125'
Dosage: text:3 g
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Ethyol
Dosage: daily dose:340mg
Start date: 2006-09-28
End date: 2006-11-06
Paracetamol
Dosage: daily dose:1gram
Start date: 2006-11-06
End date: 2006-11-07
Metoclopramide
Dosage: daily dose:60mg
Indication: Nausea
Start date: 2006-11-06
End date: 2006-11-06
Metoclopramide
Indication: Vomiting
Other drugs received by patient: Seropram; Temesta; ALL Other Therapeutic Products
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-26
Patient: 68 year old male
Adverse reactions / side effects: Vomiting, Nausea, Symblepharon, Post Procedural Complication, Conjunctival Oedema, Pseudomonas Infection, General Physical Health Deterioration, Toxic Epidermal Necrolysis, Multi-Organ Failure, Agranulocytosis, Serratia Sepsis, Staphylococcal Infection, Eye Disorder, Keratitis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Triflucan
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Ciprofloxacin
Dosage: text:1 g
Administration route: Oral
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Augmentin '125'
Dosage: text:3 g
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Ethyol
Dosage: daily dose:340mg
Start date: 2006-09-28
End date: 2006-11-06
Paracetamol
Dosage: daily dose:1gram
Start date: 2006-11-06
End date: 2006-11-07
Metoclopramide
Dosage: daily dose:60mg
Indication: Nausea
Start date: 2006-11-06
End date: 2006-11-06
Metoclopramide
Indication: Vomiting
Other drugs received by patient: Seropram; Temesta; ALL Other Therapeutic Products; Acetaminophen
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a individual with unspecified qualification from France on 2007-04-23
Patient: 68 year old male
Adverse reactions / side effects: Serratia Infection, Ulcerative Keratitis, Corneal Disorder, Bronchial Obstruction, Wound Secretion, Malaise, Catheter Related Infection, Blood Culture Positive, Hypoxia, Adhesion, Tympanic Membrane Perforation, Skin Inflammation, Dysphagia, Histiocytosis Haematophagic, Hypothermia, Pseudomonas Infection, Conjunctival Oedema, General Physical Health Deterioration, Toxic Epidermal Necrolysis, Respiratory Distress, Staphylococcal Infection, NO Therapeutic Response, Disturbance in Attention, Otitis Media, Dermatitis Exfoliative, Keratitis, Ischaemia, Symblepharon, Radiation Skin Injury, Multi-Organ Failure, Corneal Transplant, Eyelid Disorder, Pleural Effusion, Pathogen Resistance, Ear Infection, Bronchial Injury, Mucosal Inflammation, Haemoglobin Decreased, Agranulocytosis, Renal Failure, Cardiac Failure, Respiratory Failure, Oliguria, Sepsis, Leukopenia, Shock, Inflammation of Lacrimal Passage
Adverse event resulted in: life threatening event, hospitalization
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
Other drugs received by patient: Citalopram Hydrobromide; Lorazepam; Zaldiar (Paracetamol, Tramadol Hydrochloride); Acetaminophen
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a physician from France on 2007-04-18
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
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
Adverse event in 54 year old male receiving Ethyol (Amifostine)
Reported by a physician from Germany on 2007-04-09
Patient: 54 year old male
Adverse reactions / side effects: Back Pain, Aortic Arteriosclerosis, Ventricular Fibrillation, Arteriosclerosis Coronary Artery, Acute Myocardial Infarction, Intracardiac Thrombus
Adverse event resulted in: death
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Chemoradiotherapy
Adverse event in 71 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-09
Patient: 71 year old female
Adverse reactions / side effects: Injection Site Discolouration, White Blood Cell Count Decreased, Dyspnoea, Rash Generalised, Recall Phenomenon, Rash Pruritic, Injection Site Erythema, Skin Discolouration, Skin Lesion, Injection Site Reaction, Dehydration, Pharyngolaryngeal Pain, Injection Site Rash, Rash Maculo-Papular, Oxygen Saturation Decreased
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Small Cell Lung Cancer Stage Unspecified
Start date: 2007-03-12
End date: 2007-03-19
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Small Cell Lung Cancer Stage Unspecified
Start date: 2007-03-20
End date: 2007-03-23
Other drugs received by patient: Carbotaxol (Paclitaxel, Carboplatin); Radiation Therapy; Zofran
Adverse event in 80 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-29
Patient: 80 year old male, weighing 76.8 kg (169.0 pounds)
Adverse reactions / side effects: LIP Swelling, Blood Chloride Decreased, Blood Calcium Decreased, Blood Potassium Decreased, Dehydration, Blood Urea Decreased, Blood Sodium Decreased, Blood Glucose Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Unknown Chemotherappy Drug; Intensity-Modulated Radiation Therapy; Ascorbic Acid; Tylenol; Compazine
Adverse event in 63 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-20
Patient: 63 year old male, weighing 121.6 kg (267.4 pounds)
Adverse reactions / side effects: Pruritus, Rash Generalised, Swelling Face, Vomiting, Nausea, Erythema, Anxiety, Malaise, Arthralgia, Diarrhoea, Pharyngolaryngeal Pain, Dermatitis Exfoliative, Blister, Decreased Appetite
Suspect drug(s):
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Adenocarcinoma
Start date: 2006-11-28
End date: 2006-12-05
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Adenocarcinoma
Start date: 2006-12-06
End date: 2006-12-29
Other drugs received by patient: Triamterene and Hydrochlorothiazide (Hydrochlorothiazide, Triamterene); Lorazepam; Acetaminophen and Oxycodone HCL; Allegra; Kytril; Radiation Therapy
Adverse event in 50 year old male receiving Ethyol (Amifostine)
Reported by a physician from Costa Rica on 2007-02-20
Patient: 50 year old male
Adverse reactions / side effects: Rash Generalised, Hyperthermia, Anaphylactic Reaction, Hypotension
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Cisplatin; Radiation Therapy; Chemotherapy
Adverse event in 35 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-06
Patient: 35 year old female, weighing 59.4 kg (130.7 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Oral Candidiasis, Urinary Tract Infection, Platelet Count Decreased, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 1400 mg, 1 in 1 wk, intravenous (not otherwise specified)
Indication: Prophylaxis
Start date: 2006-11-22
End date: 2006-12-18
Cisplatin
Dosage: 62 mg, 1 in 1 wk
Indication: Cervix Carcinoma
Start date: 2006-11-01
End date: 2006-12-18
Other drugs received by patient: Radiation Therapy; Decadron; Compazine; Ampicillin; Levaquin; Flagyl; Nystatin
Adverse event in 50 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-19
Patient: 50 year old male, weighing 75.3 kg (165.7 pounds)
Adverse reactions / side effects: Weight Decreased, Hyperbilirubinaemia, Autoimmune Hepatitis, Chills, Hepatic Failure, Pyrexia, Biliary Cirrhosis, Thrombocytopenia, Haemochromatosis, Decreased Appetite, Vomiting, Nausea, Cold Type Haemolytic Anaemia, Haemolysis, Alpha-1 Anti-Trypsin Deficiency, Mucosal Inflammation, Neutropenia, Hepato-Lenticular Degeneration, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-10-11
End date: 2006-10-19
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-10-23
End date: 2006-10-23
Tylenol
Indication: Pyrexia
Other drugs received by patient: Diflucan; Roxicet; Zofran; Cisplatin; Radiation Therapy; Coumadin
Adverse event in male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-18
Patient: male
Adverse reactions / side effects: LIP Swelling, Dehydration
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Unknown Chemotherapy Drug; Intensity-Modulated Radiation Therapy
Adverse event in 63 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-12
Patient: 63 year old male
Adverse reactions / side effects: Malaise, Pruritus, Rash Generalised, Vomiting, Diarrhoea, Pyrexia
Suspect drug(s):
Ethyol
Dosage: see image
Indication: Adenocarcinoma
Start date: 2006-11-28
End date: 2006-01-01
Ethyol
Dosage: see image
Indication: Adenocarcinoma
Start date: 2006-01-01
End date: 2006-12-29
Other drugs received by patient: Triamterene and Hydrochlorothiazide (Hydrochlorothiazide, Triamterene); Lorazepam; Acetaminophen and Oxycodone HCL; Allegra; Kytrin (Granisetron)
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