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
90091537 9009153 7 F 201212 20160727 20130111 20160729 EXP CA-ROCHE-1172599 ROCHE 28.91 YR M Y 71.50000 KG 20160729 OT CA CA

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
90091537 9009153 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) N 125276 520 MG SOLUTION FOR INFUSION
90091537 9009153 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) N 125276 624 MG SOLUTION FOR INFUSION
90091537 9009153 3 C METHOTREXATE. METHOTREXATE 1 0
90091537 9009153 4 C PREDNISONE. PREDNISONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90091537 9009153 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
90091537 9009153 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
90091537 9009153 Bronchitis
90091537 9009153 Gingival disorder
90091537 9009153 Pneumonia
90091537 9009153 Pulmonary mass
90091537 9009153 Weight 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
90091537 9009153 1 20120203 0
90091537 9009153 2 20120328 0