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Index of reports
> Disability (15)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Orencia (Abatacept) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Orencia side effects in female
Reported by a physician from France on 2012-08-14
Patient: female
Reactions: Arthralgia, 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 40 MG / 0.8 ML PRE-Filled Syringe
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 Orencia 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 Orencia 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 Orencia 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 Orencia 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 Orencia 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
Possible Orencia side effects in 28 year old female
Reported by a consumer/non-health professional from Belgium on 2012-07-11
Patient: 28 year old female, weighing 62.0 kg (136.4 pounds)
Reactions: Disturbance in Attention, Headache, Hypersomnia
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Orencia
Other drugs received by patient: Folic Acid; Acetaminophen; Acetaminophen; Arcoxia; Pantoprazole; Methotrexate; Tramadol HCL
Possible Orencia side effects in 50 year old female
Reported by a consumer/non-health professional from Norway on 2012-07-06
Patient: 50 year old female, weighing 59.0 kg (129.8 pounds)
Reactions: Neuropathy Peripheral
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Methotrexate
Indication: Rheumatoid Arthritis
Start date: 2009-01-21
Orencia
Dosage: 10feb2009,24feb2009
Indication: Rheumatoid Arthritis
Start date: 2009-01-27
End date: 2010-08-01
Orencia
Dosage: 10feb2009,24feb2009
Indication: Gout
Start date: 2009-01-27
End date: 2010-08-01
Other drugs received by patient: Prednisolone; Folic Acid
Possible Orencia side effects in 28 year old female
Reported by a consumer/non-health professional from Belgium on 2012-07-06
Patient: 28 year old female, weighing 62.0 kg (136.4 pounds)
Reactions: Disturbance in Attention, Headache, Hypersomnia
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Orencia
Other drugs received by patient: Acetaminophen; Acetaminophen; Folic Acid; Arcoxia; Pantoprazole; Methotrexate; Tramadol HCL
Possible Orencia side effects in 54 year old female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-09
Patient: 54 year old female
Reactions: Rheumatoid Arthritis, Asthma, Sinusitis
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Methotrexate
Dosage: weekly on mondy
Administration route: Oral
Orencia
Dosage: no of infusion:3, last inf on: 3mar2012
Indication: Rheumatoid Arthritis
Start date: 2011-12-07
Other drugs received by patient: Astelin; Zyrtec; Mometasone Furoate; Albuterol; Celebrex; Neurontin; Potassium Chloride; Valium; Dyazide; Oxycodone HCL; Folic Acid; Singulair; Omnaris; Prilosec; Ultram; Nucynta
Possible Orencia side effects in 28 year old female
Reported by a health professional (non-physician/pharmacist) from Belgium on 2012-05-08
Patient: 28 year old female, weighing 62.0 kg (136.4 pounds)
Reactions: Disturbance in Attention, Headache, Hypersomnia
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Orencia
Other drugs received by patient: Methotrexate; Acetaminophen; Folic Acid; Arcoxia; Pantoprazole
Possible Orencia side effects in 51 year old male
Reported by a consumer/non-health professional from United States on 2012-02-21
Patient: 51 year old male
Reactions: Swelling
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Orencia
Possible Orencia side effects in 66 year old female
Reported by a consumer/non-health professional from United States on 2012-02-10
Patient: 66 year old female
Reactions: Arthritis
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Orencia
Other drugs received by patient: Oxycodone HCL; Prednisone TAB; Methotrexate; Plavix
Possible Orencia side effects in 55 year old
Reported by a consumer/non-health professional from Argentina on 2011-11-09
Patient: 55 year old
Reactions: Weight Decreased, Rheumatoid Arthritis, Dysphagia, Respiratory Failure, Bronchitis, Pyrexia, Respiratory Tract Infection
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Folic Acid
Methotrexate
Administration route: Oral
Naproxen
Orencia
Possible Orencia side effects in 49 year old female
Reported by a physician from Japan on 2011-10-17
Patient: 49 year old female
Reactions: Diabetes Mellitus
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Medrol
Administration route: Oral
Orencia
Dosage: admistd 3 times. therapy dates:8oct10,22oct10 57.0kg
Start date: 2010-09-24
Other drugs received by patient: Salagen; Mobic; Solu-Medrol; Lipitor
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