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
123742302 12374230 2 F 2016 20160729 20160517 20160804 EXP BR-ABBVIE-16K-020-1627982-00 ABBVIE 0.00 F Y 72.00000 KG 20160804 CN COUNTRY NOT SPECIFIED BR

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
123742302 12374230 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous LOADING DOSE, WEEK 0 UNKNOWN 125057 160 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
123742302 12374230 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous LOADING DOSE, WEEK 2 UNKNOWN 125057 80 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
123742302 12374230 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
123742302 12374230 4 C CENTRUM VITAMINS 1 Oral 0 TABLET
123742302 12374230 5 C CENTRUM VITAMINS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123742302 12374230 1 Crohn's disease
123742302 12374230 4 Vitamin supplementation
123742302 12374230 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123742302 12374230 OT
123742302 12374230 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123742302 12374230 Abdominal distension
123742302 12374230 Alopecia
123742302 12374230 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
123742302 12374230 1 20160204 20160204 0
123742302 12374230 2 20160218 20160218 0
123742302 12374230 3 2016 0
123742302 12374230 4 2008 0