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
118699213 11869921 3 F 20160725 20151228 20160728 EXP CA-AMGEN-CANSP2015138689 AMGEN 56.00 YR A F Y 0.00000 20160727 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
118699213 11869921 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
118699213 11869921 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK 0
118699213 11869921 3 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 UNK 0
118699213 11869921 4 C NAPROXEN. NAPROXEN 1 UNK 0
118699213 11869921 5 C CORTISONE CORTISONEHYDROCORTISONE 1 UNK 0
118699213 11869921 6 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
118699213 11869921 1 Rheumatoid arthritis
118699213 11869921 2 Rheumatoid arthritis
118699213 11869921 6 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
118699213 11869921 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118699213 11869921 Abasia
118699213 11869921 Drug dose omission
118699213 11869921 Drug ineffective
118699213 11869921 Hand deformity
118699213 11869921 Mobility decreased

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
118699213 11869921 2 2004 2005 0
118699213 11869921 6 20160119 0