|
Index of reports
> Cases resulting in disability (88)
Below is the selection of adverse event reports related to Humira (Adalimumab) that includes cases resulting in disability.
Reports 1 - 25 of 88 Next >>
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 male receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-25
Patient: male, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Embolism, LEG Amputation, Peripheral Ischaemia
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Sulfasalazine; Hydroxychloroquine Sulfate; Folic Acid; Thiamine; Strong B Compound; Ibuprofen
Adverse event in male receiving Humira (Adalimumab)
Reported by a physician from France on 2007-10-24
Patient: male, weighing 91.0 kg (200.2 pounds)
Adverse reactions / side effects: Monoplegia, Paraesthesia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Ketoprofen
Adverse event in female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-22
Patient: female, weighing 84.0 kg (184.8 pounds)
Adverse reactions / side effects: Rotator Cuff Syndrome
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Sulfasalazine; Methotrexate; Prednisolone; Betamethasone; Folic Acid; Indapamide; Irbesartan
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-18
Patient: male
Adverse reactions / side effects: Nasal Neoplasm, Nasal Sinus Cancer, Sensation of Pressure
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Folic Acid; Diazepam; Acetaminophen W / Codeine
Adverse event in female receiving Humira (Adalimumab)
Reported by a physician from United States on 2007-10-18
Patient: female, weighing 62.7 kg (137.8 pounds)
Adverse reactions / side effects: Weight Decreased, Drug Ineffective, Post Procedural Haematoma, Headache, Multiple Myeloma, Herpes Zoster, Synovial Cyst, Rheumatoid Arthritis, Paraplegia, Fatigue, Chest Pain, Peripheral Nerve Lesion, Spinal Cord Compression, Temperature Regulation Disorder, Nausea, Squamous Cell Carcinoma, Synovitis, Osteoma, Anorexia, Spinal Osteoarthritis
Adverse event resulted in: disablity
Suspect drug(s):
Humira
Indication: Rheumatoid Arthritis
Start date: 2004-08-01
End date: 2005-01-01
Humira
Start date: 2005-01-01
End date: 2006-12-01
Humira
End date: 2007-02-01
Other drugs received by patient: Prednisone; Prednisone; Prednisone; Valium; Alendronate Sodium; Naproxen; Fluocinonide; Ketoconazole; Lekovit CA; Lekovit CA; Omeprazole; Joint Food; Centrum Silver; Abatacept; Prednisone
Adverse event in receiving Humira (Adalimumab)
Reported by a physician from United Kingdom on 2007-10-16
Patient: , weighing 2.2 kg (4.7 pounds)
Adverse reactions / side effects: Trisomy 21
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-09
Patient: male
Adverse reactions / side effects: LEG Amputation, Peripheral Ischaemia
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Sulfasalazine; Hydroxychloroquine Sulfate; Folic Acid; Thiamine
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-30
Patient: male, weighing 60.9 kg (134.0 pounds)
Adverse reactions / side effects: Haemarthrosis, Swelling, Pain
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Paracetamol; Ibuprofen; Methotrexate Sodium; Brufen Retard
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-30
Patient: male, weighing 60.9 kg (134.0 pounds)
Adverse reactions / side effects: Meniscus Lesion, Haemarthrosis, Swelling, Pain
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Ibuprofen; Paracetamol; Methotrexate Sodium
Adverse event in male receiving Humira (Adalimumab)
Reported by a physician from Germany on 2007-07-27
Patient: male
Adverse reactions / side effects: Weight Decreased, Diabetes Mellitus, Diarrhoea, Refractory Anaemia With Ringed Sideroblasts, General Physical Health Deterioration, Pyrexia, Pneumonia Pneumococcal
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Metoprolol Succinate; Valoron Retard; Pantozpol 20; Ramipril; Aspirin; Clarithromycin; Prednisolone
Adverse event in 70 year old female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Germany on 2007-07-27
Patient: 70 year old female
Adverse reactions / side effects: Intervertebral Disc Protrusion
Adverse event resulted in: disablity
Suspect drug(s):
Humira
Indication: Drug USE FOR Unknown Indication
Start date: 2005-02-01
Methotrexate
Indication: Drug USE FOR Unknown Indication
Adverse event in male receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Germany on 2007-07-27
Patient: male
Adverse reactions / side effects: Dental Prosthesis User
Adverse event resulted in: disablity
Suspect drug(s):
Etanercept
Indication: Drug USE FOR Unknown Indication
Start date: 2005-03-01
End date: 2006-08-01
Humira
Indication: Drug USE FOR Unknown Indication
Start date: 2006-08-01
Leflunomide
Indication: Drug USE FOR Unknown Indication
Methotrexate
Indication: Drug USE FOR Unknown Indication
Start date: 2005-01-01
Adverse event in 51 year old female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Germany on 2007-07-26
Patient: 51 year old female
Adverse reactions / side effects: Tendonitis
Adverse event resulted in: disablity
Suspect drug(s):
Etanercept
Indication: Drug USE FOR Unknown Indication
Start date: 2002-03-01
End date: 2007-01-01
Etanercept
End date: 2007-01-01
Humira
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-01
Adverse event in female receiving Humira (Adalimumab)
Reported by a pharmacist from United Kingdom on 2007-07-25
Patient: female
Adverse reactions / side effects: Swelling Face, Gingival Pain, Wheezing, Oedema Peripheral, Lacrimation Increased, Toothache, Eye Pruritus
Adverse event resulted in: disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Alendronate Sodium; Atorvastatin Calcium; Aspirin; Bendroflumethiazide; Acetaminophen W / Codeine; Dihydrocodeine Bitartrate INJ; Omeprazole; Paroxetine; Prednisolone; Diltiazem HCL; Orlistat; Loratadine
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-25
Patient: male, weighing 76.0 kg (167.2 pounds)
Adverse reactions / side effects: Postoperative Wound Infection, Rheumatoid Nodule
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Sulfasalazine; Lansoprazole; Lactulose; Furosemide; Diclofenac Sodium; Leflunomide
Adverse event in female receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-23
Patient: female, weighing 69.0 kg (151.8 pounds)
Adverse reactions / side effects: Pruritus, Vision Blurred, Photopsia
Adverse event resulted in: disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Prednisolone; Amlodipine; Atenolol; Ranitidine Hydrochloride
Adverse event in female receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-20
Patient: female, weighing 52.0 kg (114.4 pounds)
Adverse reactions / side effects: Wrist Fracture
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Methotrexate; Acetylsalicylic Acid SRT; Celecoxib; Acetaminophen W / Codeine; Folic Acid; Alendronate Sodium; Omeprazole; Dipyridamole
Adverse event in female receiving Humira (Adalimumab)
Reported by a physician from United States on 2007-07-18
Patient: female, weighing 66.7 kg (146.8 pounds)
Adverse reactions / side effects: Neoplasm Malignant, Eye Swelling
Adverse event resulted in: disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Unknown Medication; Steroids
Adverse event in female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from Germany on 2007-07-16
Patient: female, weighing 88.0 kg (193.6 pounds)
Adverse reactions / side effects: Jaundice, Biliary Cirrhosis Primary, C-Reactive Protein Increased, General Physical Health Deterioration, Cholestasis, Hepatic Enzyme Increased
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Mesalazin; Meloxicam
Adverse event in female receiving Humira (Adalimumab)
Reported by a individual with unspecified qualification from United Kingdom on 2007-07-16
Patient: female, weighing 160.0 kg (352.0 pounds)
Adverse reactions / side effects: Type 2 Diabetes Mellitus, Dyspnoea, Left Ventricular Dysfunction, Pneumonia, Myocardial Infarction, Left Ventricular Failure, Mobility Decreased
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Arcoxia; Bumetanide; Etoricoxib; Prednisolone; Lansoprazole; Methotrexate; Ramipril; Atorvastatin
Adverse event in female receiving Humira (Adalimumab)
Reported by a physician from Finland on 2007-07-11
Patient: female
Adverse reactions / side effects: Hypoaesthesia, Polyneuropathy, Paraesthesia
Adverse event resulted in: disablity
Suspect drug(s):
Humira (Adalimumab)
Other drugs received by patient: Prednisolone; Tramadol HCL
Adverse event in female receiving Humira (Adalimumab)
Reported by a physician from Spain on 2007-07-11
Patient: female
Adverse reactions / side effects: Psoriasis
Adverse event resulted in: disablity
Suspect drug(s):
Humira (Adalimumab)
Adverse event in female receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-09
Patient: female, weighing 71.0 kg (156.2 pounds)
Adverse reactions / side effects: Abdominal Pain, Urinary Tract Infection, Pleural Effusion, Drug Withdrawal Syndrome, Splenic Infarction
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Humira
Indication: Rheumatoid Arthritis
Start date: 2004-03-01
End date: 2004-07-01
Humira
End date: 2004-07-15
Other drugs received by patient: Prednisolone; Amitriptyline HCL; Atenolol; Atorvastatin; Omeprazole; Methotrexate Sodium; Didronel; Clopidogrel; Codeine SUL TAB; Phosphate-Sandoz
Adverse event in male receiving Humira (Adalimumab)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-05
Patient: male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Swelling Face, Contusion, Nasopharyngitis, Pruritus, Anaphylactic Shock, 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; Atorvastatin Calcium; Pregabalin; Folic Acid
Page 1 Next >>
|
