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
118204343 11820434 3 F 2015 20160926 20151210 20160927 EXP US-ABBVIE-15K-163-1513480-00 ABBVIE 0.00 M Y 0.00000 20160927 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
118204343 11820434 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous 1044630,1061172 125057 SOLUTION FOR INJECTION IN PRE-FILLED PEN
118204343 11820434 2 C LOMOTIL ATROPINE SULFATEDIPHENOXYLATE HYDROCHLORIDE 1 0
118204343 11820434 3 C IMODIUM LOPERAMIDE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118204343 11820434 1 Crohn's disease
118204343 11820434 2 Diarrhoea
118204343 11820434 3 Diarrhoea

Outcome of event

Event ID CASEID OUTC COD
118204343 11820434 OT
118204343 11820434 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118204343 11820434 Diarrhoea
118204343 11820434 Drug ineffective
118204343 11820434 General physical health deterioration

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
118204343 11820434 1 201504 0