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Orencia (Abatacept) - Disability - Suspected Cause - Side Effect Reports

 
 



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 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 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 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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