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Cordarone (Amiodarone) - Adverse Event Reports - Life Threatening Events - Interstitial Lung Disease

 



Index of reports > Cases resulting in life threatening events (28) > Cases with Interstitial Lung Disease (5)

Below is the selection of adverse event reports related to Cordarone (Amiodarone) that includes cases resulting in life threatening events where reactions include interstitial lung disease.

Adverse event in 83 year old male receiving Cordarone (Amiodarone)

Reported by a individual with unspecified qualification from France on 2007-06-12

Patient: 83 year old male

Adverse reactions / side effects: Alveolitis, Overdose, Interstitial Lung Disease, Haemoptysis, Pleurisy, General Physical Health Deterioration

Adverse event resulted in: life threatening event

Suspect drug(s):
Bisoprolol Fumarate
    Dosage: 10 mg (10 mg, 1 d)
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-08-03
    End date: 2007-03-27

Cosopt
    Indication: Glaucoma
    End date: 2007-03-27

Crestor
    Dosage: 5 mg (5 mg, 1 d)
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-10-01
    End date: 2007-03-27

Cordarone
    Dosage: 100 mg (100 mg, 1 d)
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2004-07-01
    End date: 2007-03-27

Triamtec(5 MG, Capsule) (Ramipril)
    Dosage: 10 mg (10 mg, 1 d)
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-10-01
    End date: 2007-03-27

Other drugs received by patient: Mopral(capsule) (Omeprazole); Previscan(tablet) (Fluindione)



Adverse event in 83 year old male receiving Cordarone (Amiodarone)

Reported by a health professional (non-physician/pharmacist) from France on 2007-06-06

Patient: 83 year old male

Adverse reactions / side effects: Alveolitis, Interstitial Lung Disease

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Crestor
    Administration route: Oral
    Start date: 2006-08-01
    End date: 2007-03-27

Triatec
    Administration route: Oral
    Start date: 2006-10-01
    End date: 2007-03-27

Cosopt
    Indication: Glaucoma
    End date: 2007-03-27

Detensiel
    Administration route: Oral
    Start date: 2004-07-01
    End date: 2007-03-27

Cordarone
    Administration route: Oral
    Start date: 2004-07-01
    End date: 2007-03-27

Other drugs received by patient: Omeprazole; Previscan



Adverse event in 77 year old female receiving Cordarone (Amiodarone)

Reported by a health professional (non-physician/pharmacist) from France on 2007-04-24

Patient: 77 year old female

Adverse reactions / side effects: Renal Failure, Metabolic Alkalosis, Interstitial Lung Disease

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cordarone (Amiodarone)

Other drugs received by patient: Previscan



Adverse event in 62 year old male receiving Cordarone (Amiodarone)

Reported by a health professional (non-physician/pharmacist) from France on 2007-03-05

Patient: 62 year old male

Adverse reactions / side effects: Interstitial Lung Disease, Pseudomonas Infection, Blood Culture Positive, Pneumonia Cytomegaloviral

Adverse event resulted in: life threatening event

Suspect drug(s):
Cordarone
    Dosage: 200 mg/frequency not provided
    Administration route: Oral
    Indication: Atrial Fibrillation
    End date: 2006-10-31

Cordarone
    Indication: Arrhythmia

Cellcept
    Dosage: not provided
    End date: 2006-10-31

Cymevan
    Dosage: 140 mg/frequency not provided
    Administration route: Oral
    Start date: 2006-10-27
    End date: 2006-11-08

Sectral
    Dosage: 200mg/frequency not provided
    Administration route: Oral
    End date: 2006-10-31

Other drugs received by patient: Zeffix; Prograf; Adefovir Dipivoxil; Nexium; Pravastatin; Aspegic 1000; Fortum; Calciparine; Novomix; Cortancyl



Adverse event in 51 year old male receiving Cordarone (Amiodarone)

Reported by a individual with unspecified qualification from Sweden on 2007-01-16

Patient: 51 year old male

Adverse reactions / side effects: Neuropathy, Catheter Related Infection, Cardiac Failure, Interstitial Lung Disease, Staphylococcal Sepsis, Myocardial Infarction

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cordarone
    Dosage: 6 mg/ml (total amount administered was not provided) intravenous
    Indication: Atrial Fibrillation
    Start date: 2006-05-12
    End date: 2006-05-12

Cordarone
    Dosage: 200 mg 2x per 1 day oral
    Administration route: Oral
    Indication: Atrial Fibrillation
    Start date: 2006-05-13
    End date: 2006-05-22

Plavix
    Dosage: 75 mg 1x per 1 day oral
    Administration route: Oral
    Indication: Myocardial Infarction
    Start date: 2006-05-10
    End date: 2006-06-07

Other drugs received by patient: Plendil; Aspirin; Hytacand (Candesartan Cilexetil / Hydrochlorothiazide); Metformin HCL; Simvastatin; Furosemide; Selokeen ZOC (Metoprolol Succinate); Actrapid Human (Insulin Human); Omeprazole; Fluoxetine; Klexan (Heparin-Fraction, Sodium Salt)

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