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
123983382 12398338 2 F 2015 20160830 20160524 20160908 PER US-AMGEN-USASL2016065289 AMGEN 65.00 YR E M Y 0.00000 20160908 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
123983382 12398338 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
123983382 12398338 2 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
123983382 12398338 3 C RITUXAN RITUXIMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123983382 12398338 1 Rheumatoid arthritis
123983382 12398338 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123983382 12398338 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123983382 12398338 Arthritis
123983382 12398338 Drug effect decreased
123983382 12398338 Drug ineffective
123983382 12398338 Inflammation
123983382 12398338 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
123983382 12398338 1 200612 201506 0
123983382 12398338 2 2016 2016 0