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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Humira (Adalimumab). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (2283)
Cases resulting in a serious event (2242)
Cases resulting in death (319)
Cases resulting in life threatening events (133)
Cases resulting in hospitalization (1561)
Cases resulting in disability (88)
Cases resulting in other serious reactions (831)
Below is a sample of reports where side effects / adverse reactions may be related to Humira (Adalimumab). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in male receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-31
Patient: male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Carotid Artery Occlusion, Cerebrovascular Accident
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Sulfasalazine; Methotrexate; CO-Codydramol; Folic Acid; Naproxen
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-31
Patient: male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Swelling Face, Contusion, Nasopharyngitis, Pruritus, Anaphylactic Reaction, Adverse Drug Reaction, Petechiae, Oral Herpes, Platelet Count Decreased, Eye Swelling
Adverse event resulted in: disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Sodium Picosulfate; Fentanyl; Fentanyl; Atorvastatin Calcium; Pregabalin; Folic Acid; Lactulose; Atorvastatin Calcium; Pregabalin
Adverse event in female receiving Humira (Adalimumab)
Reported by a physician from United States on 2007-10-31
Patient: female, weighing 51.3 kg (112.9 pounds)
Adverse reactions / side effects: Road Traffic Accident, Femur Fracture
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira
Indication: Rheumatoid Arthritis
Start date: 2006-04-01
End date: 2007-05-26
Humira
Start date: 2004-01-01
End date: 2005-10-22
Humira
Start date: 2007-10-22
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-10-31
Patient: male
Adverse reactions / side effects: Drug Effect Decreased, Dysphagia, Tongue Neoplasm Malignant Stage Unspecified
Adverse event resulted in: hospitalization
Suspect drug(s):
Enbrel
Indication: Psoriatic Arthropathy
Start date: 1999-09-01
End date: 2007-08-10
Humira
Indication: Psoriatic Arthropathy
Start date: 2005-01-13
End date: 2005-07-01
Mabthera
Indication: Psoriatic Arthropathy
Start date: 2006-10-21
End date: 2007-06-26
Remicade
Dosage: 300 mg per boost
Indication: Psoriatic Arthropathy
Start date: 2005-09-01
End date: 2005-12-01
Other drugs received by patient: Prednisolon; Methotrexate
Adverse event in male receiving Humira (Adalimumab)
Reported by a physician from Norway on 2007-10-30
Patient: male
Adverse reactions / side effects: Squamous Cell Carcinoma
Adverse event resulted in: hospitalization
Suspect drug(s):
Enbrel
Enbrel
Indication: Psoriatic Arthropathy
Humira
Indication: Psoriatic Arthropathy
Remicade
Indication: Psoriatic Arthropathy
Rituxan
Indication: Psoriatic Arthropathy
Other drugs received by patient: Prednisolon; Methotrexate; Rituximab
Adverse event in female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient: female, weighing 46.0 kg (101.2 pounds)
Adverse reactions / side effects: Weight Decreased, Diarrhoea
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Lansoprazole; Calcifediol; Risedronate Sodium; Bromazepam; Auranofin; Prednisone; Methotrexate; Amlodipine; Gabapentin; Pyridoxine Hydrochloride; Pyridoxine Hydrochloride; Nico2-10; Nico2-10
Adverse event in female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-30
Patient: female, weighing 43.0 kg (94.6 pounds)
Adverse reactions / side effects: Rheumatoid Arthritis, Clostridium Difficile Colitis, Parkinson's Disease
Adverse event resulted in: death
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Prednisolone; Diazepam; Dihydrocodeine Bitartrate INJ; Ferrous Sulfate TAB; Lansoprazole; Risperidone
Adverse event in female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Brazil on 2007-10-30
Patient: female
Adverse reactions / side effects: Cardiac Arrest
Adverse event resulted in: death
Suspect drug(s):
Humira (Adalimumab)
Adverse event in male receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-30
Patient: male
Adverse reactions / side effects: Neck Mass
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Folic Acid; Tramadol HCL; Dicloferce; Lekovit CA
Adverse event in female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from United States on 2007-10-29
Patient: female
Adverse reactions / side effects: Dyspnoea, Vomiting, Nausea, Gastric Ulcer Haemorrhage, Atrial Fibrillation, Musculoskeletal Chest Pain, Cerebrovascular Accident, Gastric Ulcer, Cardiac Failure, Pleural Effusion, Myocardial Infarction
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Diclofenac Sodium
Indication: Drug USE FOR Unknown Indication
Humira
Indication: Drug USE FOR Unknown Indication
Start date: 2003-06-01
End date: 2004-03-01
Kineret
Indication: Rheumatoid Arthritis
Start date: 2003-04-01
End date: 2003-05-01
Prednisone
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Methotrexate; Protein A Immunoadsorption Column; Hydroxychloroquine Sulfate; Metoprolol Succinate; Furosemide; Levothyroxine Sodium; Esomeprazole Magnesium
Adverse event in male receiving Humira (Adalimumab)
Reported by a consumer/non-health professional from Norway on 2007-10-29
Patient: male
Adverse reactions / side effects: Dysphagia, Squamous Cell Carcinoma
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Prednisolone; Etanercept
Adverse event in female receiving Humira (Adalimumab)
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: female, weighing 63.6 kg (139.8 pounds)
Adverse reactions / side effects: Skin Ulcer, Kidney Infection, Joint Destruction
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Adverse event in male receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Netherlands on 2007-10-29
Patient: male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Pulmonary Embolism
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Prednison; Theophylline
Adverse event in male receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Ecuador on 2007-10-29
Patient: male, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Arthritis Bacterial, Acute Respiratory Distress Syndrome
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Prednisone; Lumiracoxib; Methotrexate
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-29
Patient: male
Adverse reactions / side effects: Weight Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Prednisolone; Amitriptyline HCL; Lekovit CA; Celecoxib; Diazepam; Folic Acid; Alendronate Sodium; Nitrazepam; Valproate Sodium; Alendronate Sodium; Ascorbic Acid
Adverse event in male receiving Humira (Adalimumab)
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: male, weighing 95.3 kg (209.7 pounds)
Adverse reactions / side effects: Intervertebral Disc Disorder, Drug Ineffective, Accidental Exposure
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira
Indication: Psoriatic Arthropathy
Start date: 2005-01-01
End date: 2007-01-01
Humira
Start date: 2005-01-01
End date: 2005-01-01
Humira
Indication: Psoriatic Arthropathy
Start date: 2007-01-01
Other drugs received by patient: Methotrexate; Folic Acid
Adverse event in 30 year old female receiving Humira (Adalimumab)
Reported by a physician from Spain on 2007-10-26
Patient: 30 year old female, weighing 50.0 kg (110.0 pounds)
Adverse reactions / side effects: Aphthous Stomatitis, Dysphagia, Oral Pain, Neutropenia, Oedema Mouth, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Azathioprine
Administration route: Oral
Indication: Crohn's Disease
Start date: 2007-09-19
End date: 2007-10-02
Humira
Indication: Crohn's Disease
Start date: 2007-09-24
End date: 2007-09-24
Adverse event in male receiving Humira (Adalimumab)
Reported by a consumer/non-health professional from Germany on 2007-10-26
Patient: male
Adverse reactions / side effects: Aphasia, Oedema Peripheral, Transient Ischaemic Attack
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Adverse event in male receiving Humira (Adalimumab)
Reported by a consumer/non-health professional from United States on 2007-10-26
Patient: male, weighing 77.2 kg (169.8 pounds)
Adverse reactions / side effects: Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Adverse event in female receiving Humira (Adalimumab)
Reported by a consumer/non-health professional from Finland on 2007-10-26
Patient: female
Adverse reactions / side effects: Dyspnoea, Fistula, Haemorrhage
Suspect drug(s):
Humira (Adalimumab)
Adverse event in female receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-26
Patient: female, weighing 130.0 kg (286.0 pounds)
Adverse reactions / side effects: Cellulitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Cetirizine HCL; Temazepam; Diclofenac; Tramadol HCL; Bioprolol
Adverse event in 50 year old female receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-26
Patient: 50 year old female
Adverse reactions / side effects: Sepsis, Urinary Tract Infection, Vaginal Discharge, Kidney Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Adverse event in male receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Germany on 2007-10-26
Patient: male, weighing 90.0 kg (198.0 pounds)
Adverse reactions / side effects: Malaise, Hepatic Enzyme Increased, Joint Stiffness
Adverse event resulted in: hospitalization
Suspect drug(s):
Humira (Adalimumab)
Adverse event in 50 year old female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Brazil on 2007-10-26
Patient: 50 year old female, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Back Pain, Chest Discomfort, Pain, Rhinitis, Lobar Pneumonia, Cardiac Failure, Diarrhoea, Respiratory Failure, Pleural Effusion
Adverse event resulted in: death
Suspect drug(s):
Humira
Indication: Rheumatoid Arthritis
Start date: 2007-04-01
End date: 2007-10-08
Methotrexate
Indication: Rheumatoid Arthritis
Start date: 2006-01-01
End date: 2007-10-04
Methotrexate
End date: 2001-01-01
Other drugs received by patient: Leflunomide; Prednisone; Unknown Diuretic; Captopril; Metformin
Adverse event in 73 year old female receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-26
Patient: 73 year old female, weighing 59.0 kg (129.8 pounds)
Adverse reactions / side effects: Respiratory Disorder, Troponin Increased, non-Hodgkin's Lymphoma Unspecified Histology Aggressive, Cardiac Failure Congestive, Fluid Retention, Tracheal Deviation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Humira
Indication: Rheumatoid Arthritis
Start date: 2004-10-13
End date: 2007-10-09
Methotrexate
Administration route: Oral
Indication: Rheumatoid Arthritis
Other drugs received by patient: Folic Acid; Alendronate Sodium; Levothyroxine Sodium
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