The Safety Rates Drug Report

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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
126504301 12650430 1 I 20160706 20160814 20160814 EXP CA-AMGEN-CANSP2016089419 AMGEN 51.00 YR A M Y 0.00000 20160814 CN 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
126504301 12650430 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
126504301 12650430 2 SS GOLD GOLD 1 Unknown UNK 0
126504301 12650430 3 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0
126504301 12650430 4 SS METHOTREXATE. METHOTREXATE 1 Unknown 20 MG, QWK 0 20 MG /wk
126504301 12650430 5 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 200 MG, BID 0 200 MG BID
126504301 12650430 6 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
126504301 12650430 7 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
126504301 12650430 8 SS HUMIRA ADALIMUMAB 1 Unknown UNK 0
126504301 12650430 9 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
126504301 12650430 10 SS RITUXAN RITUXIMAB 1 Unknown UNK 0
126504301 12650430 11 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown 20 MG, QD 0 20 MG QD
126504301 12650430 12 SS SULFASALAZINE. SULFASALAZINE 1 Unknown 1 G, QD 0 1 G QD
126504301 12650430 13 C PREDNISONE. PREDNISONE 1 15 MG, QD 0 15 MG QD
126504301 12650430 14 C LYRICA PREGABALIN 1 Oral UNK 0
126504301 12650430 15 C XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, BID 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126504301 12650430 1 Rheumatoid arthritis
126504301 12650430 2 Product used for unknown indication
126504301 12650430 3 Product used for unknown indication
126504301 12650430 4 Rheumatoid arthritis
126504301 12650430 5 Product used for unknown indication
126504301 12650430 6 Product used for unknown indication
126504301 12650430 7 Product used for unknown indication
126504301 12650430 8 Product used for unknown indication
126504301 12650430 9 Product used for unknown indication
126504301 12650430 10 Product used for unknown indication
126504301 12650430 11 Product used for unknown indication
126504301 12650430 12 Rheumatoid arthritis
126504301 12650430 14 Neuropathy peripheral
126504301 12650430 15 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126504301 12650430 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126504301 12650430 Arthropathy
126504301 12650430 Drug intolerance
126504301 12650430 Laboratory test abnormal
126504301 12650430 Neuropathy peripheral
126504301 12650430 Prerenal failure
126504301 12650430 Renal disorder
126504301 12650430 Treatment failure

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126504301 12650430 4 1990 2008 0
126504301 12650430 5 201001 201101 0
126504301 12650430 10 2015 0
126504301 12650430 11 2007 2008 0
126504301 12650430 12 201001 201101 0
126504301 12650430 15 20160729 0