|
Index of reports
> Cases resulting in death (46)
> Cases with Alanine Aminotransferase Increased (6)
Below is the selection of adverse event reports related to Cordarone (Amiodarone) that includes cases resulting in death where reactions include alanine aminotransferase increased.
Adverse event in 81 year old male receiving Cordarone (Amiodarone)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-04
Patient: 81 year old male, weighing 85.0 kg (187.0 pounds)
Adverse reactions / side effects: Alanine Aminotransferase Increased, Pancytopenia, Renal Failure Acute
Adverse event resulted in: death
Suspect drug(s):
Aldactone
Administration route: Oral
Start date: 2007-02-07
End date: 2007-02-19
Colchimax
Dosage: text:1 df-freq:daily
Administration route: Oral
Indication: Chondrocalcinosis
Start date: 2007-02-05
End date: 2007-02-20
Cordarone
Administration route: Oral
Flagyl
Dosage: text:3 df
Indication: Clostridium Difficile Colitis
Start date: 2007-02-14
End date: 2007-02-19
Lasix
Lovenox
Dosage: text:1 df-freq:daily
Other drugs received by patient: Tavanic; Ceftriaxone; Ventolin; Vasten; Kardegic; Imodium; Saccharomyces Boulardii; Montelukast Sodium; Zyloric ^faes^; Spiriva ^pfizer^; Imovane; Acetaminophen
Adverse event in 77 year old female receiving Cordarone (Amiodarone)
Reported by a individual with unspecified qualification from France on 2007-05-23
Patient: 77 year old female
Adverse reactions / side effects: Hyperthermia, Hypertrophic Cardiomyopathy, Hypoglycaemia, Lactic Acidosis, Prothrombin Time Prolonged, Oral Herpes, Fatigue, Cardio-Respiratory Arrest, Overdose, Hepatic Encephalopathy, Electrocardiogram QRS Complex Prolonged, Oxygen Saturation Decreased, Dyspnoea, International Normalised Ratio Increased, Alanine Aminotransferase Increased, Conduction Disorder, Blood Creatine Increased, Cardiogenic Shock, Haemodialysis, Lung Disorder, Dehydration, Aspartate Aminotransferase Increased, Ejection Fraction Decreased, Hyperthyroidism, Neuralgia
Adverse event resulted in: death
Suspect drug(s):
Cardensiel 1.25 MG (1.25 MG, Tablet) (Bisoprolol Fumarate)
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-08
Cordarone
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-20
End date: 2007-01-08
Other drugs received by patient: Preterax (Tablet) (Indapamide, Peridopril Erbumine); Previscan (Tablet) (Fluindione); Furosemide; Diffu K (Capsule) (Potassium Chloride); Amaryl; Glucophage 850 MG (Metformin)
Adverse event in 81 year old male receiving Cordarone (Amiodarone)
Reported by a individual with unspecified qualification on 2007-05-22
Patient: 81 year old male, weighing 85.0 kg (187.0 pounds)
Adverse reactions / side effects: Dyspnoea, Pneumonia, Hyperthermia, Alanine Aminotransferase Increased, Febrile Neutropenia, Hepatic Failure, Pancytopenia, Mixed Hepatocellular-Cholestatic Injury, Multi-Organ Failure, Agranulocytosis, Cardiac Failure, Diarrhoea, Sepsis, Acute Respiratory Failure, Renal Failure Acute
Adverse event resulted in: death
Suspect drug(s):
Flagyl
Administration route: Oral
Start date: 2007-02-14
End date: 2007-02-19
Lasilix / 00032601 /
Administration route: Oral
End date: 2007-02-18
Lovenox
End date: 2007-02-19
Colchimax (France)
Administration route: Oral
Start date: 2007-02-05
End date: 2007-02-20
Cordarone
Administration route: Oral
End date: 2007-02-18
Aldactone
Administration route: Oral
Start date: 2007-02-07
End date: 2007-02-19
Other drugs received by patient: Vasten / 00880402 /; Imovane; Tavanic; Ventoline / 00139501 /; Kardegic / 00002703 /; Imodium; Ultra-Levure / 00838001 /; Singulair; Spiriva; Allopurinol; Rocephin; Efferalgan / 00020001 /; Calciparine
Adverse event in female receiving Cordarone (Amiodarone)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-01
Patient: female
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Tahor
Administration route: Oral
Start date: 2007-02-01
End date: 2007-02-04
Cordarone
Dosage: daily dose:900mg
Start date: 2007-02-01
End date: 2007-02-04
Other drugs received by patient: Sertraline Hydrochloride; Cetirizine HCL; Amisulpride; Sevelamer; Acepromazine; Sodium Polystyrene Sulfonate; Tramadol Hydrochloride / Acetaminophen; Aspirin; Esomeprazole Magnesium; Quinine; Calcium Carbonate; Dipyridamole; Amoxicillin + Clavulanate Potassium; Heparin; Clopidogrel; Atenolol; Ciprofloxacin; Insulin Human
Adverse event in female receiving Cordarone (Amiodarone)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-09
Patient: female
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Tahor
Administration route: Oral
Start date: 2007-02-01
End date: 2007-02-04
Cordarone
Dosage: daily dose:900mg
Start date: 2007-02-01
End date: 2007-02-04
Other drugs received by patient: Sertraline Hydrochloride; Cetirizine HCL; Amisulpride; Sevelamer; Acepromazine; Sodium Polystyrene Sulfonate; Tramadol Hydrochloride / Acetaminophen; Aspirin; Esomeprazole Magnesium; Quinine; Calcium Carbonate; Dipyridamole; Amoxicillin + Clavulanate Potassium; Heparin; Clopidogrel; Atenolol; Ciprofloxacin; Insulin Human
Adverse event in female receiving Cordarone (Amiodarone)
Reported by a health professional (non-physician/pharmacist) from France on 2007-03-16
Patient: female
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Tahor
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-01
End date: 2007-02-04
Cordarone
Dosage: daily dose:900mg
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-01
End date: 2007-02-04
Other drugs received by patient: Sertraline Hydrochloride; Cetirizine HCL; Amisulpride; Sevelamer; Acepromazine; Sodium Polystyrene Sulfonate; Tramadol Hydrochloride / Acetaminophen; Aspirin; Esomeprazole Magnesium; Quinine; Calcium Carbonate; Dipyridamole; Amoxicillin + Clavulanate Potassium; Heparin; Clopidogrel; Atenolol; Ciprofloxacin; Insulin Human
|
