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
124651332 12465133 2 F 201310 20160627 20160614 20160706 EXP CA-ABBVIE-16K-028-1647541-00 ABBVIE 25.49 YR F Y 57.00000 KG 20160706 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
124651332 12465133 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
124651332 12465133 2 SS INFLIXIMAB INFLIXIMAB 1 Unknown U UNKNOWN 0
124651332 12465133 3 SS METHOTREXATE. METHOTREXATE 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124651332 12465133 1 Crohn's disease
124651332 12465133 2 Crohn's disease
124651332 12465133 3 Crohn's disease

Outcome of event

Event ID CASEID OUTC COD
124651332 12465133 OT
124651332 12465133 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124651332 12465133 Drug ineffective
124651332 12465133 Small 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
124651332 12465133 1 20130909 201510 0