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
125906541 12590654 1 I 20160301 20160304 20160726 20160726 EXP CA-ROCHE-1722416 ROCHE 60.86 YR F Y 0.00000 20160726 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
125906541 12590654 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) N 125276 561.6 MG SOLUTION FOR INFUSION
125906541 12590654 2 C NUCYNTA TAPENTADOL HYDROCHLORIDE 1 0
125906541 12590654 3 C GABAPENTIN. GABAPENTIN 1 0
125906541 12590654 4 C METHOTREXATE. METHOTREXATE 1 0
125906541 12590654 5 C COVERSYL PERINDOPRIL 1 0
125906541 12590654 6 C BACLOFEN. BACLOFEN 1 0
125906541 12590654 7 C FOLIC ACID. FOLIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125906541 12590654 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125906541 12590654 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125906541 12590654 Diarrhoea
125906541 12590654 Gastrointestinal pain

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
125906541 12590654 1 20160301 2016 0