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Index of reports
> Cases resulting in a serious event (78)
> Cases with Hypotension (18)
Below is the selection of adverse event reports related to Ethyol (Amifostine) that includes cases resulting in a serious event where reactions include hypotension.
Adverse event in 65 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-02
Patient: 65 year old female, weighing 83.9 kg (184.6 pounds)
Adverse reactions / side effects: Oral Intake Reduced, Radiation Skin Injury, Blood Sodium Decreased, Stevens-Johnson Syndrome, Blood Urea Increased, Cardiac Enzymes Increased, Drug Hypersensitivity, Hypotension, International Normalised Ratio Increased, Urinary Tract Infection, Atrial Fibrillation, Therapeutic Response Decreased, Brain Natriuretic Peptide Increased, Burns Second Degree, Blood Potassium Decreased, Dehydration, Pharmaceutical Product Complaint
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Neoplasm Malignant
Start date: 2007-05-15
End date: 2007-05-31
Ethyol
Ethyol
Ethyol
Other drugs received by patient: Radiation Therapy; Prinivil; Hydrochlorothiazide; Zocor; Coumadin; Norvasc; Kytril; Hydromorphone HCL; Metoprolol Tartrate; Cilostazol; Fish OIL Supplement (Fish Oil); Folic Acid
Adverse event in 82 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-26
Patient: 82 year old female
Adverse reactions / side effects: Sepsis Syndrome, Breath Sounds Abnormal, Diarrhoea, Pain in Extremity, Hypotension, Pulmonary Embolism, Pharmaceutical Product Complaint
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Ethyol
Ethyol
Ethyol
Other drugs received by patient: Radiation Therapy; Fluorouracil
Adverse event in 52 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-26
Patient: 52 year old male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Back Pain, Hypotension, Toxic Epidermal Necrolysis, Diarrhoea, Anaphylactoid Reaction, Platelet Count Decreased, Dermatitis Exfoliative, Pharmaceutical Product Complaint
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
Ethyol
Ethyol
Ethyol
Other drugs received by patient: Fluorouracil; Radiation Therapy; Zofran
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 53 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-31
Patient: 53 year old female, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Body Temperature Increased, Nausea, Chills, Hypotension, Rash Papular, Flushing, Malaise, Injection Site Erythema, Fatigue, Rash Erythematous, Asthenia, Skin Warm
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: see image
Indication: Radiotherapy
Start date: 2007-01-31
End date: 2007-01-31
Ethyol
Dosage: see image
Indication: Radiotherapy
Start date: 2007-02-08
End date: 2007-02-14
Other drugs received by patient: Benadryl; Radiation Therapy; Activella; Allegra; Ativan; Calcium with Vitamin D (Colecalciferol, Calcium Carbonate); Carafate; Corgard; Imitrex; Lunesta; Mary's Magic Mouthwash; Naproxen; Oxycontin; Protonix; Synthroid; Tenormin; :vitamin B Complex(pyridoxine Hydrochloride, Thiamine Hydrochloride, R; Wellbutrin; Zocor
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 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 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 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 73 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-02
Patient: 73 year old male
Adverse reactions / side effects: Vascular Insufficiency, Gastrointestinal Haemorrhage, Hyperkinesia, Loss of Consciousness, Blood Culture Positive, Arteriosclerosis, Cardiac Failure Congestive, Hypovolaemia, Back Pain, Cardiac Murmur, Pain in Extremity, Hypotension, Anaemia, Peptostreptococcus Infection, Respiratory Distress, Iliac Artery Stenosis, Aspartate Aminotransferase Increased, Pulse Absent, Injection Site Haemorrhage, Fall, Aspiration, Arterial Insufficiency, Tachypnoea, Thrombocytopenia, Acute Myocardial Infarction, Rash Generalised, Rash Papular, Alanine Aminotransferase Increased, Cerebral Atrophy, Hepatic Enzyme Increased, Renal Failure, Hypoproteinaemia, Respiratory Failure, Sepsis
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Cisplatin; Radiation Therapy; Zofran; Decadron; Prochlorperazine Maleate
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 57 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-12
Patient: 57 year old male, weighing 59.1 kg (130.1 pounds)
Adverse reactions / side effects: Pain, Bundle Branch Block Right, Blood Magnesium Decreased, Blood Calcium Decreased, Activated Partial Thromboplastin Time Prolonged, Myoglobin Blood Increased, Electrolyte Imbalance, Myocardial Infarction, Refusal of Treatment by Patient, Hypotension, International Normalised Ratio Increased, Haemoglobin Decreased, Renal Failure, Blood Phosphorus Decreased, Blood Potassium Decreased, Diarrhoea, Dehydration, Prothrombin Time Shortened, Platelet Count Decreased, Septic Shock
Adverse event resulted in: hospitalization
Suspect drug(s):
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2007-01-11
End date: 2007-01-22
Ethyol
Dosage: 500 mg, 5 in 5 d, subcutaneous
Indication: Radiotherapy
Start date: 2007-02-05
End date: 2007-02-05
Other drugs received by patient: Radiation Therapy; Ativan; Compazine; Cisplatin; Emend; Decadron
Adverse event in 48 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-08
Patient: 48 year old male, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Treatment Noncompliance, Neutrophil Percentage Decreased, Electrolyte Imbalance, Lethargy, Lymphocyte Count Decreased, White Blood Cell Count Decreased, Band Neutrophil Count Increased, Cellulitis, Rash Generalised, Vomiting, Nausea, Abdominal Wall Abscess, Hypotension, Dehydration, Sepsis, Feeding Tube Complication, Asthenia
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; Unknown Chemotherapy Drug; Compazine; Morphine ER (Morphine); Reglan; Prevacid; Vicodin; Oxycodone HCL; Carafate; Levaquin; Metronidazole
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 73 year old male receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-20
Patient: 73 year old male
Adverse reactions / side effects: Thrombosis, Vascular Insufficiency, Chronic Obstructive Pulmonary Disease, Loss of Consciousness, Renal Artery Stenosis, Injection Site Erythema, Arteriosclerosis, Hypovolaemia, Cardiac Failure Congestive, Back Pain, Neutrophil Count Increased, Pain in Extremity, Blood Pressure Systolic Increased, Hypotension, Catheter Site Haemorrhage, Respiratory Distress, Iliac Artery Stenosis, Aspartate Aminotransferase Increased, Platelet Count Decreased, Fall, Haematocrit Decreased, Aspiration, Arterial Insufficiency, Acute Myocardial Infarction, Thrombocytopenia, White Blood Cell Count Decreased, Refusal of Treatment by Patient, Rash Generalised, Alanine Aminotransferase Increased, Rash Papular, Condition Aggravated, Livedo Reticularis, Haemoglobin Decreased, Renal Failure, Respiratory Failure, Heart Rate Increased
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Ethyol (Amifostine)
Other drugs received by patient: Cisplatin; Radiation Therapy; Zofran; Decadron; Prochlorperazine Maleate
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 70 year old female receiving Ethyol (Amifostine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-06
Patient: 70 year old female, weighing 71.2 kg (156.7 pounds)
Adverse reactions / side effects: Radiation Oesophagitis, Blood Alkaline Phosphatase Increased, Malnutrition, Hypotension, Drug Hypersensitivity, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Chills, Post Procedural Complication, Tachycardia, Schizophrenia, Paranoid Type, Musculoskeletal Chest Pain, Dehydration, Aspartate Aminotransferase Increased, Chest Pain, Pancreatitis
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
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