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
90621593 9062159 3 F 20120504 20130619 20130127 20130630 EXP DK-TEVA-381372ISR TEVA 65.02 YR F Y 0.00000 20130630 MD DK DK

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
90621593 9062159 1 PS METHOTREXATE 1 SUBCUTANEOUS U 81099 15 MG /wk
90621593 9062159 2 SS METHOTREXATE 1 SUBCUTANEOUS U 81099
90621593 9062159 3 SS HUMIRA 1 4371.30952 MG U 0 40 MG SOLUTION FOR INJECTION QOW
90621593 9062159 4 C HYDROXYCHLOROQUINE 1 D 0
90621593 9062159 5 C SALAZOPYRIN 1 D 0
90621593 9062159 6 C METHOTREXATE 1 ORAL D 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90621593 9062159 1 Rheumatoid arthritis
90621593 9062159 3 Rheumatoid arthritis
90621593 9062159 5 Rheumatoid arthritis
90621593 9062159 6 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
90621593 9062159 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
90621593 9062159 Dermatitis
90621593 9062159 Eczema infected
90621593 9062159 Leukocytoclastic vasculitis
90621593 9062159 Pruritus
90621593 9062159 Skin plaque

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
90621593 9062159 1 20080616 20100217 0
90621593 9062159 2 20100721 20120217 0
90621593 9062159 3 20080225 20120711 0
90621593 9062159 4 20081211 20090602 0
90621593 9062159 5 20081211 20090602 0
90621593 9062159 6 20080225 20080615 0