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
125431521 12543152 1 I 20140903 20140909 20160711 20160711 EXP BR-ROCHE-1461508 ROCHE 60.99 YR F Y 56.00000 KG 20160711 CN 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
125431521 12543152 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) LAST INFUSION ON : 01-NOV-2015. U 103705 SOLUTION FOR INFUSION
125431521 12543152 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
125431521 12543152 3 C CELEBRA CELECOXIB 1 0
125431521 12543152 4 C DEFLAZACORT DEFLAZACORT 1 0
125431521 12543152 5 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 0
125431521 12543152 6 C ATORVASTATIN ATORVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125431521 12543152 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125431521 12543152 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125431521 12543152 Arthropathy
125431521 12543152 Confusional state
125431521 12543152 Dizziness
125431521 12543152 Gastroenteritis
125431521 12543152 Headache
125431521 12543152 Hypersensitivity
125431521 12543152 Immunodeficiency
125431521 12543152 Pain
125431521 12543152 Sensory disturbance
125431521 12543152 Sinusitis

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
125431521 12543152 1 20140224 0
125431521 12543152 2 20140922 0