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
119143342 11914334 2 F 2013 20160725 20160113 20160802 EXP CA-PFIZER INC-2015475521 PFIZER 81.00 YR M Y 0.00000 20160802 CN 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
119143342 11914334 1 SS ENBREL ETANERCEPT 1 50 MG, UNK N 1034008 0 50 MG
119143342 11914334 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK N 11719
119143342 11914334 3 SS SULFASALAZINE. SULFASALAZINE 1 UNK 7073
119143342 11914334 4 C REMICADE INFLIXIMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119143342 11914334 1 Rheumatoid arthritis
119143342 11914334 2 Rheumatoid arthritis
119143342 11914334 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
119143342 11914334 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119143342 11914334 Abasia
119143342 11914334 Computerised tomogram abnormal
119143342 11914334 Condition aggravated
119143342 11914334 Drug ineffective
119143342 11914334 Headache
119143342 11914334 Pain in extremity
119143342 11914334 Peripheral swelling
119143342 11914334 Rheumatoid arthritis

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
119143342 11914334 1 20121220 0