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
117982572 11798257 2 F 201509 20160725 20151203 20160802 EXP BR-ABBVIE-15K-020-1490836-00 ABBVIE 41.28 YR F Y 87.00000 KG 20160802 MD 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
117982572 11798257 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous 50061XH01 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
117982572 11798257 2 C AZATHIOPRINE. AZATHIOPRINE 1 Oral 0 TABLET
117982572 11798257 3 C NEOVLAR 2 Oral 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117982572 11798257 1 Crohn's disease
117982572 11798257 2 Crohn's disease
117982572 11798257 3 Contraception

Outcome of event

Event ID CASEID OUTC COD
117982572 11798257 HO
117982572 11798257 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117982572 11798257 Crohn's disease
117982572 11798257 Drug ineffective
117982572 11798257 Feeding disorder
117982572 11798257 Gastritis
117982572 11798257 Haematuria
117982572 11798257 Pain
117982572 11798257 Small intestine ulcer
117982572 11798257 Urinary tract infection
117982572 11798257 Vomiting
117982572 11798257 Weight decreased

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
117982572 11798257 1 20120101 201605 0
117982572 11798257 2 2015 0
117982572 11798257 3 2002 0