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
125954921 12595492 1 I 20160302 20160725 20160727 20160727 EXP CN-ROCHE-1802056 ROCHE 40.26 YR M Y 68.60000 KG 20160727 OT CN CN

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
125954921 12595492 1 PS MABTHERA RITUXIMAB 1 Intravenous drip Y H0182 103705 500 MG SOLUTION FOR INFUSION QD
125954921 12595492 2 C PARACETAMOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125954921 12595492 1 B-cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
125954921 12595492 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125954921 12595492 Chills
125954921 12595492 Dyspnoea
125954921 12595492 Palpitations

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
125954921 12595492 1 20160302 20160302 0