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
125726692 12572669 2 F 20160715 20160725 20160720 20160726 EXP BR-ROCHE-1796652 ROCHE 44.63 YR F Y 0.00000 20160726 PH 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
125726692 12572669 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) Y 103705 1000 G SOLUTION FOR INFUSION
125726692 12572669 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) RESTARTED Y 103705 SOLUTION FOR INFUSION
125726692 12572669 3 C ENALAPRIL ENALAPRIL 1 Oral ANTI-HYPERTENSIVE 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125726692 12572669 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125726692 12572669 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125726692 12572669 Abdominal discomfort
125726692 12572669 Abdominal pain
125726692 12572669 Dyspnoea
125726692 12572669 Tachycardia

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
125726692 12572669 1 20160715 20160715 0
125726692 12572669 3 2012 0