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
127525063 12752506 3 F 2016 20160920 20160916 20160930 EXP CA-AMGEN-CANSL2016122121 AMGEN 77.00 YR E M Y 0.00000 20160930 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
127525063 12752506 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, UNK U 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
127525063 12752506 2 SS ENBREL ETANERCEPT 1 U 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
127525063 12752506 3 SS NEORAL CYCLOSPORINE 1 Unknown UNK 0
127525063 12752506 4 C ADALAT NIFEDIPINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127525063 12752506 1 Psoriatic arthropathy
127525063 12752506 2 Rheumatoid arthritis
127525063 12752506 3 Blood creatinine increased

Outcome of event

Event ID CASEID OUTC COD
127525063 12752506 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127525063 12752506 Blood creatinine increased
127525063 12752506 Prostatic disorder
127525063 12752506 Psoriasis
127525063 12752506 Therapeutic response decreased

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
127525063 12752506 1 20160216 0
127525063 12752506 3 2016 2016 0