The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126827601 12682760 1 I 20160818 20160825 20160825 EXP CA-AMGEN-CANSP2016108783 AMGEN 0.00 F Y 0.00000 20160825 OT CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126827601 12682760 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
126827601 12682760 2 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
126827601 12682760 3 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0 TABLET
126827601 12682760 4 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK 0
126827601 12682760 5 SS CORTISONE CORTISONEHYDROCORTISONE 1 Unknown UNK 0 ORAL DROPS
126827601 12682760 6 SS FOLIC ACID. FOLIC ACID 1 Unknown UNK 0
126827601 12682760 7 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK 0 TABLET
126827601 12682760 8 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK 0
126827601 12682760 9 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown UNK 0 TABLET
126827601 12682760 10 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
126827601 12682760 11 SS ORENCIA ABATACEPT 1 Subcutaneous UNK 0
126827601 12682760 12 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
126827601 12682760 13 SS REACTINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNK 0
126827601 12682760 14 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
126827601 12682760 15 SS RITUXAN RITUXIMAB 1 Unknown UNK 0
126827601 12682760 16 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK 0
126827601 12682760 17 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126827601 12682760 1 Rheumatoid arthritis
126827601 12682760 2 Rheumatoid arthritis
126827601 12682760 3 Rheumatoid arthritis
126827601 12682760 4 Rheumatoid arthritis
126827601 12682760 5 Rheumatoid arthritis
126827601 12682760 6 Product used for unknown indication
126827601 12682760 7 Product used for unknown indication
126827601 12682760 8 Rheumatoid arthritis
126827601 12682760 9 Rheumatoid arthritis
126827601 12682760 10 Rheumatoid arthritis
126827601 12682760 11 Rheumatoid arthritis
126827601 12682760 12 Product used for unknown indication
126827601 12682760 13 Product used for unknown indication
126827601 12682760 14 Rheumatoid arthritis
126827601 12682760 15 Rheumatoid arthritis
126827601 12682760 16 Rheumatoid arthritis
126827601 12682760 17 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126827601 12682760 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126827601 12682760 Alopecia
126827601 12682760 Fatigue
126827601 12682760 Glossodynia
126827601 12682760 Pemphigus
126827601 12682760 Systemic lupus erythematosus

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found