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
125915842 12591584 2 F 2016 20160829 20160726 20160923 PER US-AMGEN-USASP2016093315 AMGEN 55.00 YR A M 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
125915842 12591584 1 PS ENBREL ETANERCEPT 1 Unknown UNK D 103795 UNKNOWN FORMULATION
125915842 12591584 2 SS IMURAN AZATHIOPRINE 1 Unknown UNK 0
125915842 12591584 3 C METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125915842 12591584 4 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 0
125915842 12591584 5 C XELJANZ TOFACITINIB CITRATE 1 Oral 11 MG, QD 0 11 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125915842 12591584 1 Rheumatoid arthritis
125915842 12591584 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125915842 12591584 Drug ineffective
125915842 12591584 Rash erythematous
125915842 12591584 Rash pruritic
125915842 12591584 Therapeutic response delayed

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
125915842 12591584 1 201506 2016 0
125915842 12591584 2 201202 0