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
126665911 12666591 1 I 20160626 20160817 20160819 20160819 EXP CO-ROCHE-1815729 ROCHE 62.89 YR F Y 74.00000 KG 20160819 CN CO CO

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
126665911 12666591 1 PS Tocilizumab TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 8 MG/KG SOLUTION FOR INFUSION
126665911 12666591 2 SS Tocilizumab TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 8 MG/KG SOLUTION FOR INFUSION
126665911 12666591 3 SS Tocilizumab TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 SOLUTION FOR INFUSION
126665911 12666591 4 SS Tocilizumab TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 SOLUTION FOR INFUSION
126665911 12666591 5 SS Tocilizumab TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 SOLUTION FOR INFUSION
126665911 12666591 6 C CALCITRIOL. CALCITRIOL 1 Oral 0 .25 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126665911 12666591 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126665911 12666591 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126665911 12666591 Gastric ulcer
126665911 12666591 Vomiting

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
126665911 12666591 1 20150622 0
126665911 12666591 2 20151022 0
126665911 12666591 3 20160315 0
126665911 12666591 4 20160412 0
126665911 12666591 5 20160501 0