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
100334183 10033418 3 F 2008 20160627 20140325 20160704 EXP US-AMGEN-USASP2014019846 AMGEN 27.00 YR A F Y 0.00000 20160704 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
100334183 10033418 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, TWICE A WEEK 1041948 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE BIW
100334183 10033418 2 SS ENBREL ETANERCEPT 1 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
100334183 10033418 3 SS REMICADE INFLIXIMAB 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100334183 10033418 1 Psoriasis
100334183 10033418 2 Psoriatic arthropathy
100334183 10033418 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
100334183 10033418 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100334183 10033418 Drug ineffective
100334183 10033418 Drug specific antibody present
100334183 10033418 Maternal exposure before pregnancy
100334183 10033418 Obstructed labour
100334183 10033418 Poor peripheral circulation
100334183 10033418 Psoriasis
100334183 10033418 Psoriatic arthropathy
100334183 10033418 Skin discolouration
100334183 10033418 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
100334183 10033418 1 200809 20160608 0