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
113349202 11334920 2 F 201206 20160727 20150804 20160729 EXP CA-ROCHE-1088995 ROCHE 77.37 YR F Y 59.02000 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
113349202 11334920 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 480 MG SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113349202 11334920 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
113349202 11334920 OT
113349202 11334920 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
113349202 11334920 Arthritis
113349202 11334920 Chronic obstructive pulmonary disease
113349202 11334920 Diarrhoea
113349202 11334920 Drug effect decreased
113349202 11334920 Fall
113349202 11334920 Mobility decreased
113349202 11334920 Nausea
113349202 11334920 Pain
113349202 11334920 Pain in extremity
113349202 11334920 Pneumonia

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
113349202 11334920 1 20120410 0