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
125645021 12564502 1 I 20160712 20160718 20160718 EXP CA-AMGEN-CANSP2016091087 AMGEN 0.00 F Y 0.00000 20160717 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
125645021 12564502 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
125645021 12564502 2 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
125645021 12564502 3 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
125645021 12564502 4 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125645021 12564502 1 Rheumatoid arthritis
125645021 12564502 2 Rheumatoid arthritis
125645021 12564502 3 Rheumatoid arthritis
125645021 12564502 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125645021 12564502 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125645021 12564502 Arthropathy
125645021 12564502 Diarrhoea
125645021 12564502 Drug ineffective
125645021 12564502 Lung disorder
125645021 12564502 Nausea
125645021 12564502 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found