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
110716562 11071656 2 F 201502 20160722 20150428 20160729 EXP US-ABBVIE-15K-163-1379748-00 ABBVIE 57.14 YR F Y 51.76000 KG 20160729 CN COUNTRY NOT SPECIFIED US

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
110716562 11071656 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y 1027085 125057 160 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
110716562 11071656 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y 1027085 125057 80 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
110716562 11071656 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y 1027085 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
110716562 11071656 4 C LOMOTIL ATROPINE SULFATEDIPHENOXYLATE HYDROCHLORIDE 1 0
110716562 11071656 5 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110716562 11071656 1 Crohn's disease
110716562 11071656 4 Crohn's disease
110716562 11071656 5 Insomnia

Outcome of event

Event ID CASEID OUTC COD
110716562 11071656 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110716562 11071656 Colon cancer
110716562 11071656 Drug ineffective
110716562 11071656 Proctitis

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
110716562 11071656 1 201409 201409 0
110716562 11071656 2 2014 2014 0
110716562 11071656 3 2014 201507 0