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Index of reports
> Cases with Condition Aggravated (19)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Ilaris (Canakinumab) where reactions include condition aggravated. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Ilaris side effects in female
Reported by a physician from United States on 2012-07-19
Patient: female
Reactions: Migraine, Drug Effect Decreased, Urticaria, Muckle-Wells Syndrome, Condition Aggravated, Headache, Rash, Stress, Weight Increased, Arthralgia, Feeling Abnormal, Inflammation
Drug(s) suspected as cause:
Ilaris
Dosage: 180 mg, unk
Start date: 2012-01-01
Ilaris
Dosage: 300 mg every 6 weeks
Ilaris
Dosage: 150 mg every 8 weeks
Indication: Muckle-Wells Syndrome
Start date: 2012-02-16
Ilaris
Dosage: 150 mg every 8 weeks
Start date: 2012-04-02
Other drugs received by patient: Prednisone; Prograf; Lexapro; Ferrous Sulfate TAB; Fish OIL; Mycophenolic Acid; Cellcept; Nexium; Metoprolol Succinate; Multi-Vitamins
Possible Ilaris side effects in female
Reported by a consumer/non-health professional from United States on 2012-07-19
Patient: female
Reactions: Drug Effect Decreased, Arthralgia, Urticaria, Muckle-Wells Syndrome, Condition Aggravated, Rash, Headache, Inflammation
Drug(s) suspected as cause:
Ilaris
Dosage: 150 mg, every 6 weeks
Start date: 2012-02-16
Ilaris
Dosage: 180 mg, unk
Indication: Muckle-Wells Syndrome
Start date: 2012-01-01
End date: 2012-04-02
Other drugs received by patient: Lexapro; Nexium; Multivitamin; Fish OIL; Metoprolol Succinate; Mycophenolic Acid; Ferrous Sulfate TAB; Prograf; Prednisone
Possible Ilaris side effects in female
Reported by a physician from France on 2012-07-03
Patient: female, weighing 30.0 kg (66.0 pounds)
Reactions: Nodal Arrhythmia, Hyper IGD Syndrome, Arthralgia, Incorrect Dose Administered, Condition Aggravated, Pyrexia, Rash
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Indication: Mevalonate Kinase Deficiency
Ilaris
Dosage: 150 mg every 4 weeks
Indication: Hyper IGD Syndrome
Start date: 2007-01-01
Possible Ilaris side effects in female
Reported by a physician from France on 2012-06-21
Patient: female
Reactions: Nodal Arrhythmia, Hyper IGD Syndrome, Arthralgia, Condition Aggravated, Rash, Pyrexia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Indication: Mevalonate Kinase Deficiency
Ilaris
Dosage: 150 mg, unk
Indication: Hyper IGD Syndrome
Possible Ilaris side effects in 2 year old female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-05
Patient: 2 year old female
Reactions: Clubbing, Lymphadenopathy, Histiocytosis Haematophagic, Condition Aggravated, Therapeutic Product Ineffective, Eosinophilia, Bronchiectasis, Juvenile Arthritis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Neoral
Other drugs received by patient: Folic Acid; Kineret; Prednisone; Naproxen; Methotrexate
Possible Ilaris side effects in 55 year old female
Reported by a physician from Israel on 2012-05-23
Patient: 55 year old female
Reactions: Drug Ineffective, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Condition Aggravated, Uveitis, Hepatic Enzyme Increased
Drug(s) suspected as cause:
Ilaris
Possible Ilaris side effects in female
Reported by a physician from Germany on 2012-05-21
Patient: female, weighing 62.2 kg (136.8 pounds)
Reactions: Pain, Condition Aggravated, Rash, Drug Rash With Eosinophilia and Systemic Symptoms, Juvenile Arthritis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ibuprofen
Dosage: 800 mg, (2 x1 tabl, as needed)
Administration route: Oral
Start date: 2010-06-15
End date: 2012-04-12
Ilaris
Dosage: 249 mg, unk
Indication: Juvenile Arthritis
Start date: 2010-08-02
Methotrexate
Dosage: 15 mg, qw
Administration route: Oral
Indication: Juvenile Arthritis
Start date: 2010-06-15
Etanercept
Dosage: unk
Start date: 2005-01-04
End date: 2006-05-09
Other drugs received by patient: Prednisolone; Pantoprazole; Omeprazole
Possible Ilaris side effects in 55 year old female
Reported by a physician from Israel on 2012-05-15
Patient: 55 year old female
Reactions: Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Condition Aggravated, Uveitis, Hepatic Enzyme Increased
Drug(s) suspected as cause:
Ilaris
Possible Ilaris side effects in female
Reported by a physician from Germany on 2012-05-07
Patient: female, weighing 62.2 kg (136.8 pounds)
Reactions: Pain, Condition Aggravated, Rash, Drug Rash With Eosinophilia and Systemic Symptoms, Juvenile Arthritis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ibuprofen Tablets
Dosage: unk
Start date: 2012-01-31
End date: 2012-02-01
Ilaris
Dosage: 249 mg, unk
Indication: Juvenile Arthritis
Start date: 2010-08-03
Other drugs received by patient: Omeprazole; Methotrexate; Pantoprazole
Possible Ilaris side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-07
Patient: female
Reactions: Drug Effect Decreased, Arthralgia, Urticaria, Muckle-Wells Syndrome, Condition Aggravated, Rash, Headache, Inflammation
Drug(s) suspected as cause:
Ilaris
Dosage: 150 mg, every 6 weeks
Start date: 2012-02-16
Ilaris
Dosage: 180 mg, unk
Indication: Muckle-Wells Syndrome
Start date: 2012-01-01
End date: 2012-04-02
Other drugs received by patient: Mycophenolic Acid; Metoprolol Tartrate; Nexium; Multivitamin; Prograf; Ferrous Sulfate TAB; Fish OIL; Prednisone; Lexapro
Possible Ilaris side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-01
Patient: female
Reactions: Drug Effect Decreased, Arthralgia, Urticaria, Condition Aggravated, Muckle-Wells Syndrome, Rash, Headache, Inflammation
Drug(s) suspected as cause:
Ilaris
Dosage: 180 mg, unk
Indication: Muckle-Wells Syndrome
Start date: 2012-01-01
End date: 2012-04-02
Ilaris
Dosage: 150 mg, every 6 weeks
Start date: 2012-02-16
Other drugs received by patient: Mycophenolic Acid; Prednisone; Nexium; Multivitamin; Prograf; Metoprolol Tartrate; Lexapro; Fish OIL; Ferrous Sulfate TAB
Possible Ilaris side effects in female
Reported by a physician from Germany on 2012-04-27
Patient: female, weighing 62.2 kg (136.8 pounds)
Reactions: Pain, Condition Aggravated, Rash, Drug Rash With Eosinophilia and Systemic Symptoms, Juvenile Arthritis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ibuprofen
Dosage: unk
Start date: 2012-01-31
End date: 2012-02-01
Ilaris
Dosage: 249 mg, unk
Indication: Juvenile Arthritis
Start date: 2010-08-03
Other drugs received by patient: Omeprazole; Methotrexate; Pantoprazole
Possible Ilaris side effects in female
Reported by a consumer/non-health professional from United States on 2012-04-23
Patient: female, weighing 64.0 kg (140.8 pounds)
Reactions: Drug Effect Decreased, Arthralgia, Urticaria, Condition Aggravated, Muckle-Wells Syndrome, Headache, Rash, Inflammation
Drug(s) suspected as cause:
Ilaris
Dosage: 180 mg, unk
Start date: 2012-01-01
End date: 2012-04-02
Ilaris
Dosage: 150 mg, every 6 weeks
Indication: Muckle-Wells Syndrome
Start date: 2012-02-16
Other drugs received by patient: Multivitamin; Prograf; Ferrous Sulfate TAB; Fish OIL; Mycophenolic Acid; Metoprolol Tartrate; Prednisone TAB; Lexapro; Nexium
Possible Ilaris side effects in female
Reported by a physician from Israel on 2012-03-20
Patient: female, weighing 24.3 kg (53.5 pounds)
Reactions: Viral Infection, Condition Aggravated, Platelet Count Decreased, Pyrexia, Leukopenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Possible Ilaris side effects in female
Reported by a physician from Israel on 2012-02-21
Patient: female, weighing 24.3 kg (53.5 pounds)
Reactions: Viral Infection, Condition Aggravated, Pyrexia, Leukopenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Possible Ilaris side effects in male
Reported by a physician from Italy on 2012-02-17
Patient: male, weighing 77.7 kg (170.9 pounds)
Reactions: Pneumonia, Anaemia, Condition Aggravated, Concomitant Disease Progression
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Dosage: double blinded
Indication: Cardiovascular Event Prophylaxis
Start date: 2012-01-17
Blinded NO Treatment Received
Dosage: double blinded
Indication: Cardiovascular Event Prophylaxis
Start date: 2012-01-17
Placebo
Dosage: double blinded
Indication: Cardiovascular Event Prophylaxis
Start date: 2012-01-17
Warfarin
Dosage: unk
Start date: 2011-04-29
Other drugs received by patient: Aspirin; Furosemide; Nitroglycerin; Ramipril
Possible Ilaris side effects in female
Reported by a individual with unspecified qualification from United States on 2012-01-30
Patient: female
Reactions: Haemorrhage, Condition Aggravated, Drug Administration Error, Muckle-Wells Syndrome
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Other drugs received by patient: Kineret; Steroids NOS
Possible Ilaris side effects in female
Reported by a physician from Israel on 2011-12-20
Patient: female, weighing 24.3 kg (53.5 pounds)
Reactions: Viral Infection, Condition Aggravated, Pyrexia, Leukopenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
Possible Ilaris side effects in female
Reported by a physician from Israel on 2011-12-07
Patient: female, weighing 24.3 kg (53.5 pounds)
Reactions: Viral Infection, Condition Aggravated, Pyrexia, Leukopenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ilaris
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