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Humira (Adalimumab) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (376)

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

 Reports 1 - 30 of 376   Next >>

Possible Humira side effects in female

Reported by a consumer/non-health professional from Canada on 2012-08-24

Patient: female, weighing 158.0 kg (347.6 pounds)

Reactions: Abdominal Discomfort, Impaired Healing, Diarrhoea, Abdominal Distension, Hernia, Intestinal Resection, Constipation

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira

Other drugs received by patient: Levothyroxine Sodium



Possible Humira side effects in male

Reported by a consumer/non-health professional from United States on 2012-08-24

Patient: male

Reactions: Nerve Injury, Quality of Life Decreased, Pain, Condition Aggravated, Fall, Paraesthesia, Fatigue, Neuropathy Peripheral, Oedema Peripheral, Toxic Neuropathy, Gait Disturbance, Muscle Spasms, Neuralgia, Influenza Like Illness

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira



Possible Humira side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-21

Patient: female

Reactions: Arthralgia, Expired Drug Administered, Hepatitis B

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Dosage: loading dose
    Indication: Psoriasis
    Start date: 2012-03-10

Phentermine
    Administration route: Oral
    Indication: Weight Decreased
    Start date: 2012-07-01

Prednisone
    Dosage: 7 days
    Administration route: Oral

Prednisone
    Dosage: 7 days
    Administration route: Oral
    Indication: Arthralgia

Prednisone
    Dosage: 7 days
    Administration route: Oral
    Indication: Swelling

Prednisone
    Dosage: 7 days
    Administration route: Oral

Prednisone
    Dosage: 7 days
    Administration route: Oral

Prednisone
    Dosage: 7 days
    Administration route: Oral

Stelara
    Indication: Psoriasis
    Start date: 2012-04-11
    End date: 2012-01-01

Other drugs received by patient: Tramadol HCL; Ambien; Hydroxyzine



Possible Humira side effects in male

Reported by a consumer/non-health professional from Mexico on 2012-08-17

Patient: male, weighing 49.0 kg (107.8 pounds)

Reactions: Chondropathy, Weight Decreased, Pain, Gait Disturbance

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Indication: Ankylosing Spondylitis
    Start date: 2010-04-27
    End date: 2010-06-22

Humira
    Start date: 2012-05-29

Other drugs received by patient: Allopurinol; Tramadol HCL; Asulfidine; Acetaminophen



Possible Humira side effects in 70 year old female

Reported by a physician from Argentina on 2012-08-17

Patient: 70 year old female

Reactions: Dysphagia, Myasthenia Gravis, Viith Nerve Paralysis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira



Possible Humira side effects in male

Reported by a pharmacist from France on 2012-08-15

Patient: male, weighing 87.0 kg (191.4 pounds)

Reactions: Myalgia, Migraine, Pain, Headache, Pyrexia

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira

Other drugs received by patient: Prednisone TAB



Possible Humira side effects in male

Reported by a consumer/non-health professional from Germany on 2012-08-14

Patient: male

Reactions: Weight Increased, Hypercholesterolaemia, Diabetes Mellitus

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira

Other drugs received by patient: Diclofenac



Possible Humira side effects in 48 year old female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-08-13

Patient: 48 year old female

Reactions: Rash Pustular, Rash Maculovesicular, Drug Hypersensitivity, Urticaria, Rash Erythematous, Sinusitis, Rash Pruritic

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Enbrel
    Dosage: unk
    Indication: Product Used FOR Unknown Indication

Humira
    Dosage: unk

Other drugs received by patient: Ramipril; Methotrexate; Meloxicam; Folic Acid; Losec / 00661201 /



Possible Humira side effects in female

Reported by a physician from Germany on 2012-08-10

Patient: female

Reactions: Cellulitis, C-Reactive Protein Increased, Necrosis, Lymphangitis, Aplastic Anaemia, Skin Necrosis, Empyema, Thermal Burn, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Humira
    Indication: Rheumatoid Arthritis
    Start date: 2005-12-01
    End date: 2006-12-01

Hydrocortisone
    Indication: Rheumatoid Arthritis

Methotrexate
    Administration route: Oral
    Start date: 2007-06-19

Methotrexate
    Indication: Rheumatoid Arthritis
    Start date: 2005-12-01
    End date: 2006-12-01

Other drugs received by patient: Prednisolone; Etanercept



Possible Humira side effects in female

Reported by a physician from Japan on 2012-08-07

Patient: female, weighing 58.0 kg (127.6 pounds)

Reactions: Sudden Hearing Loss, Deafness Unilateral

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira

Humira
    Indication: Psoriatic Arthropathy
    Start date: 2010-10-19
    End date: 2010-10-19

Other drugs received by patient: Rabeprazole Sodium; Beraprost Sodium; Alfacalcidol; Magnesium Oxide; Alprazolam; Pregabalin; Fluvoxamine Maleate; Methylprednisolone; Mecobalamin; Bisoprolol Fumarate; Rizatriptan Benzoate; Triazolam



Possible Humira side effects in male

Reported by a consumer/non-health professional from Mexico on 2012-08-07

Patient: male, weighing 49.0 kg (107.8 pounds)

Reactions: Chondropathy, Weight Decreased, Pain, Gait Disturbance

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Indication: Ankylosing Spondylitis
    Start date: 2010-04-27
    End date: 2010-06-22

Humira
    Start date: 2012-05-29

Other drugs received by patient: Acetaminophen; Tramadol HCL; Asulfidine; Allopurinol



Possible Humira side effects in female

Reported by a physician from Spain on 2012-08-06

Patient: female, weighing 53.0 kg (116.6 pounds)

Reactions: Neck Pain, Psoriatic Arthropathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Dosage: 1 in 15 days, week 1
    Start date: 2011-03-07

Humira
    Dosage: week zero
    Indication: Psoriasis
    Start date: 2011-03-01
    End date: 2011-03-01

Other drugs received by patient: Clorazepate Dipotassium; Xalatan; Venlafaxine HCL



Possible Humira side effects in male

Reported by a physician from United States on 2012-08-02

Patient: male

Reactions: Humerus Fracture, Postoperative Adhesion, Osteonecrosis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Humira
    Indication: Psoriasis
    Start date: 2011-04-10

Humira
    Start date: 2012-04-01

Other drugs received by patient: Ativan; Lisinopril; Lorcet-HD; Buspar; Lorcet-HD



Possible Humira side effects in 49 year old female

Reported by a pharmacist from Canada on 2012-07-27

Patient: 49 year old female

Reactions: Condition Aggravated, Headache, Fatigue, Malaise, Asthenia, Leukopenia, Cough, Influenza Like Illness

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Humira



Possible Humira side effects in 26 year old female

Reported by a lawyer from France on 2012-07-26

Patient: 26 year old female, weighing 74.0 kg (162.8 pounds)

Reactions: Paraplegia, Spinal Cord Infarction, Paresis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Humira
    Dosage: 40 mg, unk

Humira
    Dosage: 40 mg, every two weeks
    End date: 2009-11-24

Humira
    Dosage: 80 mg, unk
    Indication: Psoriasis
    Start date: 2009-08-01

Triphasil-21
    Dosage: 80 mg, single
    Administration route: Oral
    Indication: Oral Contraception
    Start date: 2008-06-01
    End date: 2009-12-01

Other drugs received by patient: Acetaminophen; Ketoprofen



Possible Humira side effects in female

Reported by a health professional (non-physician/pharmacist) from Netherlands on 2012-07-26

Patient: female

Reactions: Deafness

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira



Possible Humira side effects in female

Reported by a physician from France on 2012-07-25

Patient: female

Reactions: Back Pain, Spinal Cord Infarction, Paresis, Pain in Extremity, Diplegia, Peripheral Sensorimotor Neuropathy, Iatrogenic Injury, Spastic Paraplegia, Paraplegia, Quadriparesis, Urinary Retention, Unevaluable Event, Peripheral Motor Neuropathy, Spinal Cord Ischaemia

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Humira
    Indication: Psoriasis
    Start date: 2009-08-11
    End date: 2009-12-02

Triphasil-21
    Administration route: Oral
    Indication: Oral Contraception

Other drugs received by patient: Clobetasol Propionate; Triphasil-21; Eductyl; Daphalgan; Paroxetine HCL



Possible Humira side effects in 58 year old female

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-07-24

Patient: 58 year old female

Reactions: Sudden Hearing Loss, Deafness Unilateral, Deafness Neurosensory

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Dosage: 40 mg milligram(s), 2 week, subcutaneous
    Indication: Rheumatoid Arthritis

Hydroxychloroquine Sulfate
    Dosage: 200 mg milligram(s), 1 day, oral
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Methotrexate
    Dosage: 22.5 mg milligram(s), 1 week,
    Indication: Rheumatoid Arthritis

Other drugs received by patient: Fluticasone Propionate; Alendronate Sodium



Possible Humira side effects in female

Reported by a physician from Spain on 2012-07-24

Patient: female, weighing 60.0 kg (132.0 pounds)

Reactions: Hypoacusis, Deafness Neurosensory

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Dosage: induction
    Indication: Psoriasis
    Start date: 2010-07-08
    End date: 2010-07-08

Humira
    Start date: 2010-07-15

Other drugs received by patient: Unknown Medication; Unknown Medication



Possible Humira side effects in female

Reported by a physician from United Kingdom on 2012-07-24

Patient: female, weighing 57.8 kg (127.2 pounds)

Reactions: Pruritus, Drug Ineffective, Skin Exfoliation, Pain, General Physical Health Deterioration, Psoriasis, Stress, Rash Macular, Anxiety, Focal Segmental Glomerulosclerosis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira

Other drugs received by patient: Diprobase; Hydromol; Ispaghula Husk; Calceos; Unknown Medication; Diprosalic; Tacalcitol; Diprosalic; Aveeno; Alendronate Sodium; Simvastatin; Hydromol; Mometasone Furoate; Simvastatin; Fluoxetine HCL; Ramipril; Olive OIL; Alphosyl; Aveeno; Dovonex



Possible Humira side effects in 48 year old female

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

Patient: 48 year old female, weighing 61.0 kg (134.2 pounds)

Reactions: Crohn's Disease

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Humira
    Start date: 2012-02-27
    End date: 2012-02-27

Humira
    Indication: Crohn's Disease
    Start date: 2012-02-13
    End date: 2012-02-13

Humira
    Start date: 2012-03-12
    End date: 2012-05-14

Prednisone
    Administration route: Oral
    Start date: 2012-01-23
    End date: 2012-01-29

Prednisone
    Administration route: Oral
    Start date: 2012-02-06
    End date: 2012-02-12

Prednisone
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2011-12-19
    End date: 2012-01-01

Prednisone
    Administration route: Oral
    Start date: 2012-01-09
    End date: 2012-01-15

Prednisone
    Administration route: Oral
    Start date: 2012-01-16
    End date: 2012-01-22

Prednisone
    Administration route: Oral
    Start date: 2012-01-02
    End date: 2012-01-08

Prednisone
    Administration route: Oral
    Start date: 2012-01-30
    End date: 2012-02-05

Other drugs received by patient: Cholestagel



Possible Humira side effects in 63 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-19

Patient: 63 year old female

Reactions: Bone Fissure

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Actonel
    Dosage: 35 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-06-04
    End date: 2010-06-14

Cytotec
    Dosage: unk
    Administration route: Oral
    Start date: 1998-12-01

Enbrel
    Dosage: unk
    Indication: Rheumatoid Arthritis
    Start date: 2008-05-01
    End date: 2008-10-01

Humira
    Dosage: unk
    Indication: Rheumatoid Arthritis
    Start date: 2008-10-01
    End date: 2009-03-01

Methotrexate
    Dosage: 7.5 mg, weekly
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-02-05

Orencia
    Dosage: unk
    Indication: Rheumatoid Arthritis
    Start date: 2011-02-01

Pentasa
    Dosage: unk
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-01-01

Plaquenil
    Dosage: 400 mg, 1x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1994-12-01

Prednisone TAB
    Dosage: 8 mg, 1x/day
    Administration route: Oral
    Start date: 1995-02-20

Prednisone TAB
    Dosage: 5 mg, 1x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1995-02-20

Protelos
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2011-02-18
    End date: 2011-09-13



Possible Humira side effects in female

Reported by a physician from France on 2012-07-18

Patient: female

Reactions: Bone Fissure, Tibia Fracture

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Actonel
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-06-04
    End date: 2010-06-14

Cytotec
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 1998-12-01

Enbrel
    Indication: Rheumatoid Arthritis
    Start date: 2008-05-01
    End date: 2008-10-01

Humira
    Indication: Rheumatoid Arthritis
    Start date: 2008-10-01
    End date: 2009-03-01

Methotrexate
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-02-05

Orencia
    Indication: Rheumatoid Arthritis
    Start date: 2011-02-01

Pentasa
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-01-01

Plaquenil
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1994-12-01

Prednisone TAB
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1995-02-20

Prednisone TAB
    Administration route: Oral
    Start date: 1995-02-20

Protelos
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2011-02-18
    End date: 2011-09-13



Possible Humira side effects in 63 year old female

Reported by a consumer/non-health professional from France on 2012-07-18

Patient: 63 year old female

Reactions: Bone Fissure

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Actonel
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-06-04
    End date: 2010-06-14

Cytotec
    Administration route: Oral
    Start date: 1998-12-01

Enbrel
    Start date: 2008-05-01
    End date: 2008-10-01

Humira
    Start date: 2008-10-01
    End date: 2009-03-01

Methotrexate
    Administration route: Oral
    Start date: 1996-02-05

Orencia
    Indication: Rheumatoid Arthritis
    Start date: 2011-02-01

Pentasa
    Administration route: Oral
    Start date: 1996-01-01

Plaquenil
    Administration route: Oral
    Start date: 1994-12-01

Prednisone TAB
    Dosage: also taken 8mg
    Administration route: Oral
    Start date: 1995-02-20

Protelos
    Indication: Osteoporosis
    Start date: 2011-02-18
    End date: 2011-09-13



Possible Humira side effects in female

Reported by a lawyer from Denmark on 2012-07-18

Patient: female, weighing 60.0 kg (132.0 pounds)

Reactions: Polyneuropathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira

Other drugs received by patient: Roacterma; Enbrel



Possible Humira side effects in 58 year old female

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-07-18

Patient: 58 year old female

Reactions: Sudden Hearing Loss, Deafness Unilateral, Deafness Neurosensory

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Indication: Rheumatoid Arthritis
    Start date: 2006-01-01

Hydroxychloroquine Sulfate
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Methotrexate
    Indication: Rheumatoid Arthritis

Other drugs received by patient: Alendronate Sodium; Fluticasone Propionate



Possible Humira side effects in 58 year old female

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-07-18

Patient: 58 year old female

Reactions: Deafness Unilateral, Deafness Neurosensory

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Dosage: 40 mg, qw2
    Indication: Rheumatoid Arthritis
    Start date: 2006-01-01

Hydroxychloroquine Sulfate
    Dosage: 200 mg, qd
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Methotrexate
    Dosage: 22.5 mg, qw
    Indication: Rheumatoid Arthritis

Other drugs received by patient: Fluticasone Propionate; Alendronate Sodium



Possible Humira side effects in female

Reported by a physician from Spain on 2012-07-17

Patient: female, weighing 53.0 kg (116.6 pounds)

Reactions: Neck Pain, Psoriatic Arthropathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Humira
    Dosage: week zero
    Indication: Psoriasis
    Start date: 2011-03-01
    End date: 2011-03-01

Humira
    Dosage: 1 in 15 days, week 1
    Start date: 2011-03-07

Other drugs received by patient: Venlafaxine HCL; Clorazepate Dipotassium; Xalatan; Acetaminophen



Possible Humira side effects in 63 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-17

Patient: 63 year old female

Reactions: Bone Fissure

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Actonel
    Dosage: 35 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-06-04
    End date: 2010-06-14

Cytotec
    Dosage: unk
    Administration route: Oral
    Start date: 1998-12-01

Enbrel
    Dosage: unk
    Indication: Rheumatoid Arthritis
    Start date: 2008-05-01
    End date: 2008-10-01

Humira
    Dosage: unk
    Indication: Rheumatoid Arthritis
    Start date: 2008-10-01
    End date: 2009-03-01

Methotrexate
    Dosage: 7.5 mg, weekly
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-02-05

Orencia
    Dosage: unk
    Indication: Rheumatoid Arthritis
    Start date: 2011-02-01

Pentasa
    Dosage: unk
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-01-01

Plaquenil
    Dosage: 400 mg, 1x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1994-12-01

Prednisone TAB
    Dosage: 8 mg, 1x/day
    Administration route: Oral
    Start date: 1995-02-20

Prednisone TAB
    Dosage: 5 mg, 1x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1995-02-20

Protelos
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2011-02-18
    End date: 2011-09-13



Possible Humira side effects in 63 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-17

Patient: 63 year old female

Reactions: Bone Fissure

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Actonel
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-06-04
    End date: 2010-06-14

Cytotec
    Administration route: Oral
    Start date: 1998-12-01

Etanercept
    Indication: Rheumatoid Arthritis
    Start date: 1998-05-01
    End date: 1998-10-01

Humira
    Indication: Rheumatoid Arthritis
    Start date: 2008-10-01
    End date: 2009-03-01

Methotrexate
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-02-05

Orencia
    Indication: Rheumatoid Arthritis
    Start date: 2011-02-01

Pentasa
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1996-01-01

Plaquenil
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1994-12-01

Prednisone TAB
    Administration route: Oral
    Start date: 1995-02-20

Prednisone TAB
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1995-02-20

Strontium Ranelate
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2011-02-18
    End date: 2011-09-13



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