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
127693461 12769346 1 I 20160909 20160921 20160921 PER US-AMGEN-USASL2016123821 AMGEN 51.00 YR A F Y 0.00000 20160921 MD 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
127693461 12769346 1 PS ENBREL ETANERCEPT 1 Unknown 25 MG, 2 TIMES/WK D 103795 25 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE BIW
127693461 12769346 2 SS ENBREL ETANERCEPT 1 Unknown 25 MG, 2 TIMES/WK D 103795 25 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE BIW
127693461 12769346 3 SS NEULASTA PEGFILGRASTIM 1 Unknown UNK 0 UNKNOWN FORMULATION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127693461 12769346 1 Rheumatoid arthritis
127693461 12769346 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127693461 12769346 Infectious colitis
127693461 12769346 Upper respiratory tract infection

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
127693461 12769346 1 201512 0
127693461 12769346 2 201608 0
127693461 12769346 3 201512 201608 0