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
124909442 12490944 2 F 1999 20160913 20160623 20160922 PER US-AMGEN-USASP2016078539 AMGEN 49.00 YR A F Y 0.00000 20160922 CN US US

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
124909442 12490944 1 PS ENBREL ETANERCEPT 1 Unknown 20 MG, QWK 103795 20 MG UNKNOWN FORMULATION /wk
124909442 12490944 2 SS ENBREL ETANERCEPT 1 Unknown UNK 103795 UNKNOWN FORMULATION
124909442 12490944 3 SS SIMPONI GOLIMUMAB 1 Unknown UNK 0
124909442 12490944 4 SS ORENCIA ABATACEPT 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124909442 12490944 1 Rheumatoid arthritis
124909442 12490944 3 Product used for unknown indication
124909442 12490944 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124909442 12490944 Abdominal discomfort
124909442 12490944 Drug ineffective
124909442 12490944 Off label use

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
124909442 12490944 1 1999 2012 0
124909442 12490944 2 201411 201507 0
124909442 12490944 4 201512 201602 0