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
123355672 12335567 2 F 20160415 20160718 20160505 20160726 EXP DE-ABBVIE-16K-062-1618026-00 ABBVIE 53.71 YR F Y 0.00000 20160726 CN COUNTRY NOT SPECIFIED DE

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
123355672 12335567 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y U 1045393 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
123355672 12335567 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y U 1045393 125057 SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
123355672 12335567 3 C L-THYROXINE LEVOTHYROXINE 1 0
123355672 12335567 4 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
123355672 12335567 5 C AZATHIOPRINE. AZATHIOPRINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123355672 12335567 1 Crohn's disease
123355672 12335567 3 Product used for unknown indication
123355672 12335567 4 Product used for unknown indication
123355672 12335567 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123355672 12335567 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123355672 12335567 Gastrointestinal disorder
123355672 12335567 Gastrointestinal necrosis
123355672 12335567 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
123355672 12335567 1 20151025 201604 0
123355672 12335567 2 20160628 0