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
126052381 12605238 1 I 20160219 20160725 20160729 20160729 EXP CN-ROCHE-1802071 ROCHE 50.00 YR M Y 77.00000 KG 20160729 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
126052381 12605238 1 PS MABTHERA RITUXIMAB 1 Intravenous drip Y H0182 103705 100 MG SOLUTION FOR INFUSION QD
126052381 12605238 2 C SODIUM CHLORIDE. SODIUM CHLORIDE 1 Intravenous drip G1512043 0 100 ML QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126052381 12605238 1 T-cell lymphoma stage IV

Outcome of event

Event ID CASEID OUTC COD
126052381 12605238 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126052381 12605238 Arrhythmia
126052381 12605238 Chest discomfort
126052381 12605238 Chills
126052381 12605238 Dyspnoea
126052381 12605238 Fear
126052381 12605238 Hyperhidrosis
126052381 12605238 Pyrexia

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
126052381 12605238 1 20160219 20160219 0
126052381 12605238 2 20160219 20160219 0