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
117531316 11753131 6 F 201509 20160920 20151119 20160922 EXP CA-ROCHE-1633393 ROCHE 49.77 YR F Y 60.00000 KG 20160922 MD 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
117531316 11753131 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 560 MG SOLUTION FOR INFUSION
117531316 11753131 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) ON HOLD U 125276 300 MG SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117531316 11753131 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
117531316 11753131 LT
117531316 11753131 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117531316 11753131 Cerebrovascular accident
117531316 11753131 Hepatic enzyme increased
117531316 11753131 Joint swelling
117531316 11753131 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
117531316 11753131 1 20150617 0
117531316 11753131 2 20150910 0