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
127020901 12702090 1 I 20160825 20160829 20160831 20160831 EXP IL-ROCHE-1822204 ROCHE 0.00 F Y 0.00000 20160831 CN IL IL

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
127020901 12702090 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 103705 600 MG SOLUTION FOR INFUSION
127020901 12702090 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 103705 600 MG SOLUTION FOR INFUSION
127020901 12702090 3 C ACAMOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127020901 12702090 1 Renal disorder

Outcome of event

Event ID CASEID OUTC COD
127020901 12702090 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127020901 12702090 Asthenia
127020901 12702090 Back pain
127020901 12702090 Dizziness
127020901 12702090 Heart rate decreased
127020901 12702090 Hypotension
127020901 12702090 Loss of consciousness

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
127020901 12702090 1 201603 0
127020901 12702090 2 20160825 0