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
125624661 12562466 1 I 20160712 20160715 20160715 EXP CA-AMGEN-CANSP2016090710 AMGEN 40.00 YR A M Y 0.00000 20160715 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
125624661 12562466 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 UNKNOWN FORMULATION
125624661 12562466 2 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
125624661 12562466 3 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
125624661 12562466 4 SS ANAKINRA ANAKINRA 1 Unknown UNK 0
125624661 12562466 5 SS ANAKINRA ANAKINRA 1 Unknown UNK 0
125624661 12562466 6 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0 TABLET
125624661 12562466 7 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0 TABLET
125624661 12562466 8 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK 0
125624661 12562466 9 SS HUMIRA ADALIMUMAB 1 Unknown UNK 0
125624661 12562466 10 SS HYDROXYCHLOROQUINE SULFATE. HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0
125624661 12562466 11 SS HYDROXYCHLOROQUINE SULFATE. HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0
125624661 12562466 12 SS HYDROXYCHLOROQUINE SULFATE. HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0
125624661 12562466 13 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125624661 12562466 14 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125624661 12562466 15 SS ORENCIA ABATACEPT 1 Unknown UNK 0
125624661 12562466 16 SS ORENCIA ABATACEPT 1 Unknown UNK 0
125624661 12562466 17 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
125624661 12562466 18 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
125624661 12562466 19 SS SIMPONI GOLIMUMAB 1 Unknown UNK 0
125624661 12562466 20 SS SIMPONI GOLIMUMAB 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125624661 12562466 1 Product used for unknown indication
125624661 12562466 2 Product used for unknown indication
125624661 12562466 4 Product used for unknown indication
125624661 12562466 6 Product used for unknown indication
125624661 12562466 8 Product used for unknown indication
125624661 12562466 10 Product used for unknown indication
125624661 12562466 13 Product used for unknown indication
125624661 12562466 15 Product used for unknown indication
125624661 12562466 17 Product used for unknown indication
125624661 12562466 19 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125624661 12562466 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125624661 12562466 Abasia
125624661 12562466 Drug dependence
125624661 12562466 Drug effect decreased
125624661 12562466 Drug specific antibody present
125624661 12562466 Muscular weakness
125624661 12562466 Nausea
125624661 12562466 Rheumatoid arthritis
125624661 12562466 Treatment failure

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

no results found

Therapies reported

no results found