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
109646964 10964696 4 F 201502 20160722 20150329 20160726 EXP DE-ROCHE-1557041 ROCHE 0.00 F Y 0.00000 20160726 CN DE DE

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
109646964 10964696 1 PS RoActemra TOCILIZUMAB 1 Subcutaneous 125472 162 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
109646964 10964696 2 SS RoActemra TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 SOLUTION FOR INFUSION
109646964 10964696 3 SS METHOTREXATE. METHOTREXATE 1 Unknown U 0
109646964 10964696 4 C INSULIN INSULIN NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109646964 10964696 1 Rheumatoid arthritis
109646964 10964696 2 Rheumatoid arthritis
109646964 10964696 3 Rheumatoid arthritis
109646964 10964696 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
109646964 10964696 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109646964 10964696 Arthralgia
109646964 10964696 Drug effect decreased
109646964 10964696 White blood cell count decreased

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
109646964 10964696 1 20140728 20150228 0
109646964 10964696 2 20150315 0