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Index of reports
> Cases resulting in a serious event (78)
> Cases with Pyrexia (23)
Below is the selection of adverse event reports related to Ethyol (Amifostine) that includes cases resulting in a serious event where reactions include pyrexia.
Adverse event in 65 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-14
Patient: 65 year old female, weighing 185.0 kg (407.0 pounds)
Adverse reactions / side effects: Mucosal Erosion, Drug Eruption, Radiation Injury, Chills, Haematuria, Pyrexia, Blood Pressure Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Radiation Therapy; Prinivil; Hydrochlorothiazide; Zocor; Coumadin; Norvasc; Kytril; Hydromorphone HCL
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 69 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-31
Patient: 69 year old male, weighing 72.3 kg (159.2 pounds)
Adverse reactions / side effects: Dyspnoea, Injection Site Erythema, Chills, Injection Site Rash, Pyrexia, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: see imate
Indication: Radiotherapy
Start date: 2007-01-24
End date: 2007-02-04
Ethyol
Dosage: see imate
Indication: Radiotherapy
Start date: 2007-02-04
End date: 2007-02-09
Other drugs received by patient: Radiation Therapy; Esophagitis Mixture; Lunesta; Mary's Magic Mouthwash; Nexium; Thorazine; Tylenol; Benadryl
Adverse event in 52 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-29
Patient: 52 year old male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Vomiting, Nausea, Chills, Hypotension, Petechiae, Pyrexia, Rash, Diarrhoea, Dermatitis Exfoliative
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Prophylaxis
Start date: 2007-04-17
End date: 2007-04-30
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Rectal Cancer
Start date: 2007-04-17
End date: 2007-04-30
Other drugs received by patient: Fluorouracil; Radiation Therapy; Zofran
Adverse event in 54 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-01
Patient: 54 year old male, weighing 118.8 kg (261.5 pounds)
Adverse reactions / side effects: Radiation Injury, Chills, Pain of Skin, Skin Burning Sensation, Pyrexia, Rash, Erythema, Malaise, Injection Site Erythema, Pharyngolaryngeal Pain, Oral Mucosa Erosion
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, daily with radiation therapy, subcutaneous
Indication: Prophylaxis
Start date: 2006-12-05
End date: 2007-01-02
Ethyol
Dosage: 500 mg, daily with radiation therapy, subcutaneous
Indication: Prophylaxis
Start date: 2007-01-03
End date: 2007-01-03
Other drugs received by patient: Interferon (Interferon); Glucotrol; Glipizide; Lexapro; Salagen; Compazine; Capitol W / Codeine (Codeine Phosphate, Paractamol); Radiation Therapy
Adverse event in 68 year old male receiving Ethyol (Amifostine)
Reported by a consumer/non-health professional from France on 2007-04-23
Patient: 68 year old male
Adverse reactions / side effects: Serratia Infection, Ulcerative Keratitis, Pyrexia, Bronchial Obstruction, Haemodynamic Instability, Poor Peripheral Circulation, Hypoxia, Dysphagia, Histiocytosis Haematophagic, Hypothermia, Eye Infection Bacterial, Hypotension, Conjunctival Oedema, Toxic Epidermal Necrolysis, Staphylococcal Sepsis, Respiratory Distress, Conjunctival Disorder, Disturbance in Attention, Ear Pain, Otitis Media, Septic Shock, Keratitis, Skin Exfoliation, Corneal Perforation, Head Injury, Symblepharon, Eye Operation, Somnolence, Fall, Glasgow Coma Scale Abnormal, Ventricular Hypertrophy, Lacrimal Disorder, Skin Discolouration, Skin Lesion, Pleural Effusion, Rash Pustular, Skin Disorder, Iris Adhesions, Rash Macular, Mucosal Inflammation, Renal Failure, Iris Disorder, Oliguria, Leukopenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Augmentin '125'
Dosage: 3g per day
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
Triflucan
Indication: Infection Parasitic
Start date: 2006-11-06
End date: 2006-11-09
Ethyol
Dosage: 340mg three times per week
Start date: 2006-09-28
End date: 2006-11-06
Ciprofloxacin HCL
Dosage: 500mg twice per day
Administration route: Oral
Indication: Infection
Start date: 2006-11-06
End date: 2006-11-09
Ciprofloxacin HCL
Dosage: 500mg twice per day
Administration route: Oral
Indication: Infection Parasitic
Start date: 2006-11-06
End date: 2006-11-09
Perfalgan
Dosage: 1g per day
Start date: 2006-11-06
End date: 2006-11-07
Primperan INJ
Dosage: 60mg per day
Indication: Nausea
Start date: 2006-11-06
End date: 2006-11-06
Other drugs received by patient: Seropram; Temesta; Acetaminophen and Tramadol HCL; Acetaminophen; Radiotherapy; Morphine; Tranxene; Kytril; Rehydration
Adverse event in 51 year old male receiving Ethyol (Amifostine)
Reported by a consumer/non-health professional from United States on 2007-04-23
Patient: 51 year old male, weighing 83.0 kg (182.6 pounds)
Adverse reactions / side effects: Eye Discharge, Chills, Pyrexia, Injection Site Erythema, Hypoaesthesia Facial, Pharyngolaryngeal Pain, White Blood Cell Count Decreased, Neutrophil Percentage Increased, Vomiting, Rash Generalised, Nausea, Drug Hypersensitivity, Mucosal Inflammation, Haemoglobin Decreased, Ocular Hyperaemia, Heart Rate Increased, Dehydration, Platelet Count Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Cisplatin; Lasix; Dolasetron (Dolasetron); Decadron; Zofran; Radiation Therapy
Adverse event in 53 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-09
Patient: 53 year old male, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Pain in Extremity, Pyrexia, Erythema, Secretion Discharge, Neoplasm Recurrence, Skin Ulcer, Skin Discolouration, Finger Amputation, Oedema Peripheral
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-12-27
End date: 2007-01-26
Erbitux
Dosage: intravenous (not otherwise specified)
Indication: Neoplasm Malignant
End date: 2007-01-12
Other drugs received by patient: Radiation Therapy; Cisplatin; Taxotere; Protonix; Decadron
Adverse event in 51 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-09
Patient: 51 year old male, weighing 83.0 kg (182.6 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Eye Discharge, Chills, Drug Hypersensitivity, Pyrexia, Computerised Tomogram Abnormal, Tremor, Haemoglobin Decreased, Mucosal Inflammation, Injection Site Erythema, Ocular Hyperaemia, DRY Throat, Hypoaesthesia Facial, Pharyngolaryngeal Pain, Candidiasis
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Radiation Therapy; Cisplatin; Lasix; Dolasetron (Dolasetron); Decadron; Zofran
Adverse event in 48 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-23
Patient: 48 year old male, weighing 149.9 kg (329.8 pounds)
Adverse reactions / side effects: Cellulitis, Vomiting, Nausea, Abdominal Wall Abscess, Chills, Hypotension, Pyrexia, Dehydration, Sepsis, Feeding Tube Complication, Electrolyte Imbalance, Asthenia, Lethargy
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: see image
Indication: Radiotherapy
Start date: 2007-01-17
End date: 2007-01-17
Ethyol
Dosage: see image
Indication: Radiotherapy
Start date: 2007-01-19
End date: 2007-01-19
Ethyol
Dosage: see image
Indication: Radiotherapy
Start date: 2007-01-23
End date: 2007-01-23
Ethyol
Dosage: see image
Indication: Radiotherapy
Start date: 2007-01-29
End date: 2007-01-29
Other drugs received by patient: Radiation Therapy; Unknown Chemotherapy Drug; Compazine; Morphine ER (Morphine); Reglan; Prevacid; Vicodin; Oxycodone HCL; Carafate; Levaquin; Metronidazole
Adverse event in 65 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-15
Patient: 65 year old male
Adverse reactions / side effects: White Blood Cell Count Decreased, Chest Discomfort, Hypotension, Chills, Urine Output Decreased, Pyrexia, Blood Creatine Increased, Injection Site Erythema, Respiratory Failure, Heart Rate Increased, Sleep Apnoea Syndrome, Blood Glucose Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Diovan; Radiation Therapy; Carboplatin; Taxol; Alprazolam; Cimetidine; Dexamethasone Sodium Phosphate; Diphenhydramine HCL; Lidocaine-Prilocaine (Lidocaine, Prilocaine); Lorazepam; Palonosetron HCL (Palonosetron Hydrochloride); Advair Diskus (Fluticasone Propionate, Salmeterol Xinafoate); EC Aspirin (Acetylsalicylic Acid); Albuterol Sulfate; Centrum Silver (Ascorbic Acid, Tocopheryl Acetate, Retinol, Zinc, Calc; Furosemide; Humulin (Insulin Human); Humulin R; Lopid; Singulair; Spiriva
Adverse event in 59 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-12
Patient: 59 year old male, weighing 63.6 kg (140.0 pounds)
Adverse reactions / side effects: Oral Intake Reduced, Skin Chapped, Weight Decreased, Pruritus, Skin Exfoliation, Chills, Pain, Radiation Skin Injury, Skin Burning Sensation, Pyrexia, Malaise, Pharyngolaryngeal Pain, Stomatitis, Nausea, Rash Papular, Mucosal Erosion, Mucosal Inflammation, Dehydration
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-10-26
End date: 2006-11-24
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Tongue Neoplasm Malignant Stage Unspecified
Start date: 2006-10-26
End date: 2006-11-24
Other drugs received by patient: Radiation Therapy; Unknown Chemotherapy Drug; Norvasc; Simvastatin; Isosorbide (Isosorbide); Niacib (Nicotinic Acid); Oxycodone HCL
Adverse event in 56 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-14
Patient: 56 year old male
Adverse reactions / side effects: Injection Site Erythema, Malaise, Chills, Injection Site Rash, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-09-12
End date: 2006-09-24
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-09-25
End date: 2006-09-29
Other drugs received by patient: Radiation Therapy; Unknown Chemotherapy Drug
Adverse event in 70 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-09
Patient: 70 year old female, weighing 71.2 kg (156.7 pounds)
Adverse reactions / side effects: Abdominal Pain, Hypersensitivity, Tachycardia, Schizophrenia, Pyrexia, Oral Candidiasis, C-Reactive Protein Increased, Oxygen Saturation Decreased, Blood Alkaline Phosphatase Increased, Radiation Oesophagitis, Vomiting, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Hypotension, Malnutrition, Musculoskeletal Chest Pain, Dehydration, Aspartate Aminotransferase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: non-Small Cell Lung Cancer Stage III
Start date: 2006-10-16
End date: 2006-10-31
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Prophylaxis
Start date: 2006-10-16
End date: 2006-10-31
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: non-Small Cell Lung Cancer Stage III
Start date: 2006-11-09
End date: 2006-11-09
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Prophylaxis
Start date: 2006-11-09
End date: 2006-11-09
Other drugs received by patient: Carboplatin; Radiation Therapy; Taxol; Celexa; Zofran; Morphine Sulfate; Compazine; Xanax; Ativan; Protonix; Nystatin; Tylenol; Kytril; Diflucan
Adverse event in 48 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-09
Patient: 48 year old male, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Vomiting, Nausea, Pyrexia, Rash, Lethargy
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2007-01-17
End date: 2007-01-17
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2007-01-19
End date: 2007-01-19
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2007-01-23
End date: 2007-01-23
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2007-01-29
End date: 2007-01-29
Other drugs received by patient: Radiation Therapy; Compazine; Morphine ER (Morphine); Reglan; Prevacid; Vicodin
Adverse event in 52 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-09
Patient: 52 year old male, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Pain in Extremity, Skin Discolouration, Skin Ulcer, Oedema Peripheral, Pyrexia, Erythema, Wound Secretion
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-12-27
End date: 2007-01-26
Erbitux
Dosage: intravenous (not otherwise specified)
Indication: Neoplasm Malignant
End date: 2007-01-12
Other drugs received by patient: Radiation Therapy; Cisplatin; Taxotere; Protonix; Decadron
Adverse event in 56 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-26
Patient: 56 year old male
Adverse reactions / side effects: Malaise, Chills, Injection Site Rash, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-09-12
End date: 2006-09-24
Ethyol
Dosage: 500 mg, 1 in 1 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-09-25
End date: 2006-09-29
Other drugs received by patient: Radiation Therapy; Unknown Chemotherapy Drug
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 59 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-19
Patient: 59 year old male, weighing 63.6 kg (140.0 pounds)
Adverse reactions / side effects: Oral Intake Reduced, Skin Chapped, Weight Decreased, Pruritus, Skin Exfoliation, Chills, Pain, Radiation Skin Injury, Skin Burning Sensation, Pyrexia, Malaise, Impaired Self-Care, Pharyngolaryngeal Pain, Stomatitis, Nausea, Pain of Skin, Rash Papular, Skin Disorder, DRY Skin, Mucosal Erosion, Mucosal Inflammation, Dehydration, Fluid Intake Reduced
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2006-10-26
End date: 2006-11-24
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Tongue Neoplasm Malignant Stage Unspecified
Start date: 2006-10-26
End date: 2006-11-24
Other drugs received by patient: Radiation Therapy; Unknown Chemotherapy Drug; Norvasc; Simvastatin; Isosorbide (Isosorbide); Lisinopril; Niacin; Oxycodone HCL
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)
Adverse event in 38 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-12
Patient: 38 year old male, weighing 91.2 kg (200.6 pounds)
Adverse reactions / side effects: Vomiting, Skin Exfoliation, Nausea, Pain of Skin, Petechiae, Skin Burning Sensation, Rash, Pyrexia, Erythema, Odynophagia, Haemoglobin Decreased, Haematocrit Decreased, Malaise, Dehydration, Skin Lesion, Pharyngolaryngeal Pain
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Radiation Therapy; Cisplatin; Mannitol; Radiosensitizer; Ativan; Decadron; Zofran
Adverse event in 71 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-12
Patient: 71 year old male, weighing 89.4 kg (196.6 pounds)
Adverse reactions / side effects: Weight Decreased, Back Pain, Chills, Rash, Pyrexia, Tremor, Dysuria, Dizziness, Neutropenia, Heart Rate Irregular, Blood Pressure Decreased, Decreased Appetite
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Radiation Therapy
Adverse event in 59 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-12
Patient: 59 year old male, weighing 63.6 kg (140.0 pounds)
Adverse reactions / side effects: Skin Chapped, Pruritus, Skin Exfoliation, Chills, Skin Burning Sensation, Pyrexia, Feeling Cold, Malaise, Skin Lesion, Pharyngolaryngeal Pain, Stomatitis, Pain of Skin, DRY Skin, Rash, Mucosal Erosion, Mucosal Inflammation, Dehydration
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Norvasc; Simvastatin; Isosorbide (Isosorbide); Lisinopril; Niacin; Oxycodone HCL; Radiation Therapy
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