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Soliris (Eculizumab) - Death - Suspected Cause - Side Effect Reports

 
 



Index of reports > Death (181)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Soliris (Eculizumab) death. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 181   Next >>

Possible Soliris side effects in male

Reported by a consumer/non-health professional from United States on 2012-08-27

Patient: male, weighing 65.0 kg (143.0 pounds)

Reactions: Death, Muscular Weakness, Mental Status Changes, Fall

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Soliris
    Dosage: 600 mg, qw
    Start date: 2012-05-02
    End date: 2012-05-23

Soliris
    Dosage: 900 mg, single
    Indication: Paroxysmal Nocturnal Haemoglobinuria
    Start date: 2012-05-30
    End date: 2012-05-30

Other drugs received by patient: Compazine; Coumadin; Zofran; Neurontin; Prednisone TAB; Prednisone TAB; Revlimid; Revlimid



Possible Soliris side effects in female

Reported by a physician from Brazil on 2012-08-27

Patient: female

Reactions: Myalgia, Arthralgia, Meningococcal Sepsis

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris
    Dosage: 900 mg, q2w
    Indication: Paroxysmal Nocturnal Haemoglobinuria
    Start date: 2011-04-19
    End date: 2012-04-04

Soliris
    Dosage: 900 mg, q2w
    Start date: 2011-09-08
    End date: 2012-04-13

Other drugs received by patient: Warfarin Sodium



Possible Soliris side effects in female

Reported by a physician from United States on 2012-08-27

Patient: female, weighing 74.0 kg (162.8 pounds)

Reactions: Intra-Abdominal Haemorrhage, Syncope, Splenic Rupture

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris

Other drugs received by patient: Calcium Carbonate; Coreg; Aranesp; Valcyte; Ascorbic Acid; Iron; Amlodipine; Vitamin D; Cyclosporine; Lasix; Magnesium Oxide; Myfortic; Pentamidine; Folic Acid; Prednisone TAB; Valcyte



Possible Soliris side effects in 40 year old female

Reported by a physician from United States on 2012-08-23

Patient: 40 year old female

Reactions: Renal Failure, Breast Cancer Metastatic, Hepatic Failure

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a individual with unspecified qualification from United States on 2012-08-22

Patient: female

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a physician from United Kingdom on 2012-08-22

Patient: female

Reactions: Cerebral Infarction, Condition Aggravated, Pupil Fixed, Bradycardia, Haemolytic Uraemic Syndrome, Intracranial Pressure Increased, Escherichia Infection

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris

Other drugs received by patient: Antibiotics



Possible Soliris side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-22

Patient: female

Reactions: Disease Progression

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris
    Dosage: 600 mg, qw
    Indication: Paroxysmal Nocturnal Haemoglobinuria
    Start date: 2008-03-11
    End date: 2008-04-01

Soliris
    Dosage: 900 mg, q2w
    Start date: 2008-04-08
    End date: 2009-10-13



Possible Soliris side effects in male

Reported by a physician from United States on 2012-08-21

Patient: male

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a physician from United States on 2012-08-21

Patient: female

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a individual with unspecified qualification from United States on 2012-08-15

Patient: female

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in male

Reported by a pharmacist from United Kingdom on 2012-08-14

Patient: male

Reactions: Confusional State, Cyanosis, Cold Type Haemolytic Anaemia, Condition Aggravated, Asthenia, Eating Disorder

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris

Other drugs received by patient: Blood and Related Products



Possible Soliris side effects in female

Reported by a physician from United States on 2012-08-14

Patient: female

Reactions: Condition Aggravated, Cardiac Failure Congestive

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-14

Patient: female

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in male

Reported by a consumer/non-health professional from Lithuania on 2012-08-03

Patient: male

Reactions: Cerebrovascular Accident

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris

Other drugs received by patient: Alphacalcidol; Erythropoetin; Beta Blockers; Human Growth Hormone, Recombinant; Acfi; Imidasoline Receptor Agonists; Aspirin



Possible Soliris side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-01

Patient: female

Reactions: Sepsis

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in male

Reported by a physician from United States on 2012-07-25

Patient: male, weighing 65.0 kg (143.0 pounds)

Reactions: Death, Muscular Weakness, Mental Status Changes, Fall

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Soliris
    Dosage: 600 mg, qw
    Start date: 2012-05-02
    End date: 2012-05-23

Soliris
    Dosage: 900 mg, single
    Indication: Paroxysmal Nocturnal Haemoglobinuria
    Start date: 2012-05-30
    End date: 2012-05-30

Other drugs received by patient: Prednisone; Revlimid; Zofran; Compazine; Revlimid; Coumadin; Prednisone; Neurontin



Possible Soliris side effects in female

Reported by a consumer/non-health professional from United States on 2012-07-23

Patient: female

Reactions: Dyspnoea, Cyanosis, Unresponsive To Stimuli, Embolic Stroke

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in

Reported by a individual with unspecified qualification from United States on 2012-07-23

Patient:

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a pharmacist from Belgium on 2012-07-23

Patient: female

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris
    Dosage: 600 mg, unk
    Indication: Paroxysmal Nocturnal Haemoglobinuria
    Start date: 2008-10-16

Soliris
    Dosage: 900 mg, unk
    Start date: 2008-11-14
    End date: 2012-07-04

Other drugs received by patient: Prednisone



Possible Soliris side effects in

Reported by a physician from France on 2012-07-20

Patient:

Reactions: Aspergillosis, Cardiac Arrest

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in

Reported by a pharmacist from Germany on 2012-07-19

Patient:

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in 27 year old female

Reported by a physician from United States on 2012-07-13

Patient: 27 year old female

Reactions: Sepsis, Pancreatitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Soliris
    Dosage: 900 mg, unk
    Start date: 2012-07-01

Soliris
    Dosage: 600 mg, unk
    Indication: Haemolytic Uraemic Syndrome
    Start date: 2012-06-30

Other drugs received by patient: Ciprofloxacin HCL



Possible Soliris side effects in male

Reported by a consumer/non-health professional from Austria on 2012-07-12

Patient: male

Reactions: Colon Cancer

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Soliris
    Dosage: unk
    Indication: Paroxysmal Nocturnal Haemoglobinuria
    Start date: 2009-01-01
    End date: 2009-01-01

Soliris
    Dosage: 900 mg, q2w
    Start date: 2009-01-01



Possible Soliris side effects in male

Reported by a physician from United States on 2012-07-11

Patient: male

Reactions: Hypotension, Condition Aggravated, Hepatic Failure, Multi-Organ Failure, Renal Failure, Intestinal Perforation, Enterococcus Test Positive, Pancreatitis, Septic Shock, Thrombocytopenia

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a physician from Brazil on 2012-07-06

Patient: female

Reactions: Myalgia, Meningitis Meningococcal, Arthralgia

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris
    Dosage: 900 mg, q2w
    Start date: 2011-09-08
    End date: 2012-04-13

Soliris
    Dosage: unk
    Indication: Paroxysmal Nocturnal Haemoglobinuria
    Start date: 2011-05-01

Other drugs received by patient: Warfarin Sodium



Possible Soliris side effects in male

Reported by a physician from United States on 2012-07-06

Patient: male

Reactions: Multi-Organ Failure, Septic Shock

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in female

Reported by a individual with unspecified qualification from United States on 2012-06-27

Patient: female

Reactions: Dyspnoea, Cyanosis, Unresponsive To Stimuli, Embolic Stroke

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in male

Reported by a consumer/non-health professional from United States on 2012-06-27

Patient: male, weighing 99.8 kg (219.6 pounds)

Reactions: Enterococcal Infection, Aspiration, Respiratory Failure, Colitis, Upper Gastrointestinal Haemorrhage, Septic Shock, Clostridial Infection, Enteritis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Soliris
    Dosage: 1200 mg, single
    Indication: Malignant Atrophic Papulosis
    Start date: 2012-03-15
    End date: 2012-03-15

Soliris
    Dosage: 900 mg, qw
    Start date: 2011-02-01

Other drugs received by patient: Fluticasone; Magnesium Sulfate; Sucralfate; Percocet; Morphine Sulfate; Hydrocortisone Sodium Succinate; Norepinephrine Bitartrate; Vancomycin; Nexium; Vancomycin; Prednisone TAB; Sarna; Oxycodone HCL; Hydrocortisone Sodium Succinate; Fragmin; Immune Globulin NOS; Vancomycin; Flagyl; Linezolid; Enoxaparin; Folic Acid; Ondansetron (Zofran); Micafungin; Potassium Chloride; Dextrose Water; Linezolid; Ethacrynic Acid; Fexofenadine; Imipenem / Cilastatin; Sodium Phosphate; Albuterol; Miconazole; Multi-Vitamin; Ondansetron (Zofran); Pantoprazole; Levofloxacin; Lisinopril; Cholestyramine; Omeprazole; Morphine Sulfate



Possible Soliris side effects in 23 month old

Reported by a pharmacist from France on 2012-06-26

Patient: 23 month old , weighing 13.0 kg (28.6 pounds)

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



Possible Soliris side effects in male

Reported by a individual with unspecified qualification from United States on 2012-06-25

Patient: male

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Soliris



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