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
119918143 11991814 3 F 20160127 20160714 20160203 20160721 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-006917 BRISTOL MYERS SQUIBB 66.89 YR F Y 0.00000 20160721 OT 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
119918143 11991814 1 PS ORENCIA ABATACEPT 1 Subcutaneous 1 UNIT, QWK Y 125118 1 DF SOLUTION FOR INJECTION /wk
119918143 11991814 2 SS ORENCIA ABATACEPT 1 Subcutaneous 125 MG, QWK Y 125118 125 MG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119918143 11991814 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119918143 11991814 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119918143 11991814 Asthma
119918143 11991814 Colonoscopy
119918143 11991814 Peripheral swelling
119918143 11991814 Pyrexia
119918143 11991814 Thrombosis
119918143 11991814 Upper respiratory tract infection
119918143 11991814 Viral infection
119918143 11991814 Wheezing

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found