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
125685292 12568529 2 F 20160910 20160719 20160916 EXP BR-ROCHE-1796671 ROCHE 45.00 YR F Y 0.00000 20160916 MD BR BR

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
125685292 12568529 1 PS MABTHERA RITUXIMAB 1 Unknown U 103705

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125685292 12568529 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125685292 12568529 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125685292 12568529 Headache
125685292 12568529 Myalgia
125685292 12568529 Nausea
125685292 12568529 Rash
125685292 12568529 Thrombocytopenia

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

no results found

Therapies reported

no results found