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Index of reports
> Life Threatening Events (38)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Lucentis (Ranibizumab) life threatening events. The selected reports were submitted to the FDA during the sample period of about a year.
Reports 1 - 30 of 38 Next >>
Possible Lucentis side effects in female
Reported by a physician from Canada on 2012-08-27
Patient: female, weighing 86.0 kg (189.2 pounds)
Reactions: Angina Unstable, Proteinuria
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Avastin
Indication: Product Used FOR Unknown Indication
Lucentis
Indication: Product Used FOR Unknown Indication
Other drugs received by patient: Metoprolol Tartrate; Risedronate Sodium; Diovan; Lansoprazole; Novolin 70 / 30; Plavix; Lipitor; Amlodipine; Gabapentin; Calcium Carbonate
Possible Lucentis side effects in 81 year old female
Reported by a physician from Switzerland on 2012-08-20
Patient: 81 year old female
Reactions: Cerebral Infarction
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Other drugs received by patient: Atorvastatin Calcium
Possible Lucentis side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-07
Patient: female
Reactions: Myocardial Infarction
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Lucentis
Indication: AGE-Related Macular Degeneration
Lucentis
Indication: Choroidal Neovascularisation
Start date: 2012-05-11
End date: 2012-05-15
Other drugs received by patient: Potassium; Levothroid; Vitamin; Plavix
Possible Lucentis side effects in male
Reported by a consumer/non-health professional from United States on 2012-08-06
Patient: male, weighing 83.5 kg (183.6 pounds)
Reactions: Electrocardiogram QT Prolonged, Dyspnoea, Chest Discomfort, Atrial Fibrillation, Cardiomyopathy, Cardiac Failure Congestive
Adverse event resulted in: life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in 88 year old female
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-07-30
Patient: 88 year old female
Reactions: Myocardial Infarction
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Lucentis
Other drugs received by patient: Adcal; Atorvastatin; Pantoprazole; Nitroglycerin; Metformin Hydrochloride; Ticagrelor; Verapamil; Aspirin; Ismn; Candesartan; Levothyroxine Sodium
Possible Lucentis side effects in 74 year old female
Reported by a physician from Switzerland on 2012-07-20
Patient: 74 year old female
Reactions: Cerebral Infarction
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Indication: Diabetic Retinal Oedema
Start date: 2012-04-30
Pravastatin
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Other drugs received by patient: Plavix; Metoprolol Tartrate; Torsemide; Insulin; Amiodarone HCL
Possible Lucentis side effects in 81 year old female
Reported by a physician from Switzerland on 2012-07-20
Patient: 81 year old female
Reactions: Cerebral Infarction
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in 81 year old female
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2012-07-10
Patient: 81 year old female
Reactions: Cerebral Infarction
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Lucentis
Dosage: third dose
Start date: 2011-05-25
Lucentis
Dosage: first dose
Indication: AGE-Related Macular Degeneration
Start date: 2011-03-30
Lucentis
Dosage: second dose
Possible Lucentis side effects in 79 year old female
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-07-04
Patient: 79 year old female
Reactions: Cerebrovascular Accident
Adverse event resulted in: life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Lucentis
Indication: AGE-Related Macular Degeneration
Start date: 2009-09-24
Lucentis
Start date: 2010-05-24
End date: 2010-05-24
Other drugs received by patient: Carbamazepine; Montelukast; Levothyroxine Sodium; Warfarin Sodium; Omeprazole; Citalopram Hydrobromide
Possible Lucentis side effects in
Reported by a physician from Germany on 2012-06-07
Patient:
Reactions: Cerebrovascular Accident
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Other drugs received by patient: Aquaphor 40; Marcumar; Lasix; Candesartan Cilexetil; Dipyrone TAB; Benoxinate Hydrochloride; Carvedilol; Allopurinol
Possible Lucentis side effects in 77 year old male
Reported by a physician from Switzerland on 2012-05-17
Patient: 77 year old male
Reactions: Gouty Arthritis, Aortic Stenosis, Coronary Artery Disease, Benign Prostatic Hyperplasia, Cognitive Disorder, Anaemia Macrocytic, Cardiac Disorder, Renal Failure, Mitral Valve Incompetence, Peripheral Arterial Occlusive Disease, Hypertension
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in 69 year old male
Reported by a physician from Switzerland on 2012-05-16
Patient: 69 year old male
Reactions: Arterial Stenosis
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in 80 year old female
Reported by a physician from Switzerland on 2012-05-14
Patient: 80 year old female
Reactions: Pulmonary Embolism
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Hydrocortisone
Administration route: Oral
Indication: Temporal Arteritis
Lucentis
End date: 2011-10-20
Lucentis
Lucentis
Indication: AGE-Related Macular Degeneration
Start date: 2008-12-08
Lucentis
Lucentis
Lucentis
Possible Lucentis side effects in 82 year old female
Reported by a physician from Switzerland on 2012-05-14
Patient: 82 year old female
Reactions: Cerebral Infarction, Transient Ischaemic Attack
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Cortisone Acetate
Administration route: Oral
Indication: Arthritis
Lucentis
Indication: AGE-Related Macular Degeneration
Start date: 2010-12-07
Lucentis
Start date: 2011-06-09
Other drugs received by patient: Hydrocortisone
Possible Lucentis side effects in female
Reported by a physician from Canada on 2012-05-02
Patient: female
Reactions: Gastrointestinal Haemorrhage, Myocardial Infarction
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Avastin
Indication: Product Used FOR Unknown Indication
Lucentis
Indication: AGE-Related Macular Degeneration
Possible Lucentis side effects in male
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-03-29
Patient: male
Reactions: Pneumonia Aspiration, Cerebrovascular Accident
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in 80 year old female
Reported by a consumer/non-health professional from Switzerland on 2012-03-21
Patient: 80 year old female
Reactions: Cardiac Arrest
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in 80 year old female
Reported by a physician from Brazil on 2012-03-16
Patient: 80 year old female
Reactions: Pulmonary Embolism
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Indication: Product Used FOR Unknown Indication
Lucentis
Start date: 2012-01-04
Other drugs received by patient: Omeprazole Magnesium; Botox; Clonazepam; Levothyroxine Sodium; Dramin; Lipitor
Possible Lucentis side effects in female
Reported by a physician from Spain on 2012-02-29
Patient: female
Reactions: Inappropriate Schedule of Drug Administration, Acute Myocardial Infarction
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Lucentis
Start date: 2012-01-01
End date: 2012-01-17
Lucentis
Dosage: in left eye
Indication: AGE-Related Macular Degeneration
Start date: 2011-03-01
Lucentis
Start date: 2011-06-01
Lucentis
Start date: 2011-11-01
Lucentis
Start date: 2011-05-01
Lucentis
Start date: 2011-07-01
End date: 2011-07-01
Lucentis
Start date: 2011-10-01
Lucentis
Start date: 2011-12-01
Lucentis
Start date: 2011-04-01
Possible Lucentis side effects in 70 year old female
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-01-24
Patient: 70 year old female
Reactions: Thalamus Haemorrhage, Cerebral Haemorrhage
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Other drugs received by patient: Citalopram Hydrobromide; Prednisolone; Simvastatin; Solifenacin Succinate; Amitriptyline HCL; Omeprazole; Acetylcysteine
Possible Lucentis side effects in male
Reported by a physician from United Kingdom on 2012-01-17
Patient: male
Reactions: Hepatic Neoplasm Malignant
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in female
Reported by a physician from United Kingdom on 2012-01-02
Patient: female
Reactions: Pneumonia, Sepsis, Myocardial Infarction
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Other drugs received by patient: Adcal-D3; Aspirin
Possible Lucentis side effects in 75 year old male
Reported by a physician from Germany on 2011-11-28
Patient: 75 year old male, weighing 97.1 kg (213.6 pounds)
Reactions: Tubulointerstitial Nephritis, Dyspnoea, Fibrin D Dimer Increased, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Allopurinol
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2007-01-01
End date: 2011-08-15
Avodart
Administration route: Oral
Indication: Benign Prostatic Hyperplasia
Start date: 2009-01-01
Furosemide
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2010-02-01
End date: 2011-08-15
Lucentis
Indication: Macular Degeneration
Start date: 2011-07-07
Other drugs received by patient: Insulin Basal; Escor; Clopidogrel; Human Insulin; Ramipril
Possible Lucentis side effects in female
Reported by a physician from United Kingdom on 2011-11-25
Patient: female
Reactions: International Normalised Ratio Increased, Fall, Lower Respiratory Tract Infection, Pulseless Electrical Activity, Haematoma
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Other drugs received by patient: Buspirone Hydrochloride; Omeprazole; Acetaminophen; CO-Amilofruse; Codeine Phosphate; Levothyroxine Sodium
Possible Lucentis side effects in female
Reported by a physician from Norway on 2011-11-21
Patient: female
Reactions: Renal Failure, Malaise, Angina Pectoris, Myocardial Ischaemia, Anaemia, Myocardial Infarction
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Alendronate Sodium
Administration route: Oral
Indication: Osteoporosis
Start date: 2011-01-01
Lucentis
Indication: Macular Degeneration
Start date: 2009-06-22
End date: 2011-04-26
Other drugs received by patient: Centyl MED Kaliumklorid; Diural (Denmark)
Possible Lucentis side effects in 75 year old male
Reported by a physician from Germany on 2011-11-21
Patient: 75 year old male, weighing 97.0 kg (213.4 pounds)
Reactions: Tubulointerstitial Nephritis, Dyspnoea, Fibrin D Dimer Increased, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Allopurinol
Dosage: 150 mg, qd
Administration route: Oral
Start date: 2007-01-01
End date: 2011-08-15
Avodart
Dosage: 0.5 mg, qd
Administration route: Oral
Indication: Benign Prostatic Hyperplasia
Start date: 2009-01-01
Furosemide
Dosage: 40 mg, qd
Administration route: Oral
Start date: 2010-02-01
End date: 2011-08-15
Lucentis
Dosage: 1 df, unk
Indication: Macular Degeneration
Start date: 2011-07-07
Other drugs received by patient: Human Insulin; Escor; Clopidogrel; Insulin Basal; Ramipril
Possible Lucentis side effects in 57 year old male
Reported by a physician from United States on 2011-11-17
Patient: 57 year old male
Reactions: Myocardial Infarction
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Lucentis
Dosage: 0.5 mg
Indication: Retinal Vein Occlusion
Start date: 2011-07-21
End date: 2011-11-16
Lucentis
Dosage: 0.5 mg
Indication: Macular Oedema
Start date: 2011-07-21
End date: 2011-11-16
Possible Lucentis side effects in 75 year old male
Reported by a physician from Germany on 2011-11-16
Patient: 75 year old male, weighing 97.1 kg (213.6 pounds)
Reactions: Tubulointerstitial Nephritis, Dyspnoea, Fibrin D Dimer Increased, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Allopurinol
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2007-01-01
End date: 2011-08-15
Avodart
Administration route: Oral
Indication: Benign Prostatic Hyperplasia
Start date: 2009-01-01
End date: 2011-08-15
Furosemide
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2010-02-01
End date: 2011-08-15
Lucentis
Indication: Macular Degeneration
Start date: 2011-07-07
Other drugs received by patient: Clopidogrel; Insulin Basal; Human Insulin; Ramipril; Escor
Possible Lucentis side effects in
Reported by a physician from India on 2011-11-16
Patient:
Reactions: Corneal Erosion
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Lucentis
Possible Lucentis side effects in female
Reported by a health professional (non-physician/pharmacist) from Norway on 2011-11-10
Patient: female
Reactions: Malaise, Renal Failure, Angina Pectoris, Anaemia, Myocardial Ischaemia, Myocardial Infarction
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Alendronate Sodium
Dosage: 70 mg, qw
Administration route: Oral
Indication: Osteoporosis
Start date: 2011-01-01
Lucentis
Dosage: 0.5 mg, qmo
Indication: Macular Degeneration
Start date: 2009-06-22
End date: 2011-04-26
Other drugs received by patient: Centyl MED Kaliumklorid; Diural
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