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
122242142 12224214 2 F 20160712 20160330 20160725 EXP E2B_00215835 CA-HQ SPECIALTY-CA-2016INT000130 INTERCHEM 56.00 YR F Y 0.00000 20160725 MD 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
122242142 12224214 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK 201749
122242142 12224214 2 SS ENBREL ETANERCEPT 1 UNK N 0
122242142 12224214 3 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 UNK N 0 TABLET
122242142 12224214 4 SS REMICADE INFLIXIMAB 1 UNK N 0
122242142 12224214 5 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 MG (5 MG,2 IN 1 D) 0 5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122242142 12224214 1 Rheumatoid arthritis
122242142 12224214 2 Rheumatoid arthritis
122242142 12224214 3 Rheumatoid arthritis
122242142 12224214 4 Rheumatoid arthritis
122242142 12224214 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122242142 12224214 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122242142 12224214 Drug ineffective
122242142 12224214 Pain in extremity
122242142 12224214 Peripheral swelling

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
122242142 12224214 2 2010 0
122242142 12224214 5 20141216 0