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
125411111 12541111 1 I 20160623 20160708 20160708 EXP CA-HQ SPECIALTY-CA-2016INT000481 INTERCHEM 51.00 YR M Y 0.00000 20160708 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
125411111 12541111 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK N 201749
125411111 12541111 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 MG (5 MG, 2 IN 1 D) 0 5 MG
125411111 12541111 3 SS IMURAN AZATHIOPRINE 1 Unknown UNK N 0
125411111 12541111 4 SS METHOTREXATE. METHOTREXATE 1 Subcutaneous 2.8571 MG (20 MG, 1 IN 1 W) 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125411111 12541111 1 Rheumatoid arthritis
125411111 12541111 2 Rheumatoid arthritis
125411111 12541111 3 Rheumatoid arthritis
125411111 12541111 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125411111 12541111 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125411111 12541111 Rheumatoid arthritis

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
125411111 12541111 2 20150528 0
125411111 12541111 3 201507 0