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
111513106 11151310 6 F 2015 20160725 20150601 20160802 EXP CA-ABBVIE-15K-028-1399682-00 ABBVIE 34.74 YR M Y 0.00000 20160802 MD COUNTRY NOT SPECIFIED 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
111513106 11151310 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
111513106 11151310 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
111513106 11151310 3 C IMURAN AZATHIOPRINE 1 Oral 0 50 MG
111513106 11151310 4 C IMURAN AZATHIOPRINE 1 Oral 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111513106 11151310 1 Crohn's disease
111513106 11151310 3 Crohn's disease

Outcome of event

Event ID CASEID OUTC COD
111513106 11151310 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
111513106 11151310 Drug ineffective
111513106 11151310 Gastrointestinal inflammation
111513106 11151310 Haematochezia
111513106 11151310 Intestinal mucosal hypertrophy
111513106 11151310 Intestinal obstruction

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
111513106 11151310 1 20140722 2015 0
111513106 11151310 2 2015 2016 0