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
126015011 12601501 1 I 20160725 20160728 20160728 EXP CA-AMGEN-CANSP2016096788 AMGEN 60.00 YR A F Y 0.00000 20160728 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
126015011 12601501 1 PS ENBREL ETANERCEPT 1 Subcutaneous 25 MG, 2 TIMES/WK U 103795 25 MG UNKNOWN FORMULATION BIW
126015011 12601501 2 SS ANAKINRA ANAKINRA 1 Unknown UNK 0
126015011 12601501 3 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown UNK 0 TABLET
126015011 12601501 4 SS IMURAN AZATHIOPRINE 1 Unknown UNK 0
126015011 12601501 5 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown UNK 0 TABLET
126015011 12601501 6 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
126015011 12601501 7 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK 0
126015011 12601501 8 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126015011 12601501 1 Rheumatoid arthritis
126015011 12601501 2 Rheumatoid arthritis
126015011 12601501 3 Rheumatoid arthritis
126015011 12601501 4 Rheumatoid arthritis
126015011 12601501 5 Rheumatoid arthritis
126015011 12601501 6 Rheumatoid arthritis
126015011 12601501 7 Rheumatoid arthritis
126015011 12601501 8 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126015011 12601501 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126015011 12601501 Drug ineffective
126015011 12601501 Rheumatoid arthritis

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

no results found

Therapies reported

no results found