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
127533542 12753354 2 F 201502 20160907 20160916 20160920 EXP FR-AMGEN-FRANI2016116828 AMGEN 34.00 YR A F Y 110.00000 KG 20160919 OT FR FR

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
127533542 12753354 1 PS etanercept ETANERCEPT 1 Subcutaneous 50 MG, BID Y 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE BID
127533542 12753354 2 SS etanercept ETANERCEPT 1 Unknown UNK Y 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127533542 12753354 1 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
127533542 12753354 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127533542 12753354 Confusional state
127533542 12753354 Fatigue
127533542 12753354 Nausea
127533542 12753354 Vomiting

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
127533542 12753354 1 201502 201503 0
127533542 12753354 2 20150511 0