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
99637842 9963784 2 F 20130201 20140825 20140305 20141001 EXP US-ABBVIE-13P-163-1117482-00 ABBVIE 44.03 YR M Y 0.00000 20141001 N 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
99637842 9963784 1 PS HUMIRA ADALIMUMAB 1 D UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
99637842 9963784 2 C DILANTIN PHENYTOIN 1 5 TABS IN MORNING AND 5 TABS AT NIGHT D 0 5 DF TABLET BID
99637842 9963784 3 C MVI VITAMINS 1 ONE DAILY D 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99637842 9963784 1 Crohn's disease
99637842 9963784 2 Seizure
99637842 9963784 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
99637842 9963784 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
99637842 9963784 Abdominal pain
99637842 9963784 Faecal volume decreased
99637842 9963784 Fistula discharge
99637842 9963784 Flatulence
99637842 9963784 Gastrointestinal stoma complication
99637842 9963784 Haemorrhage
99637842 9963784 Infected fistula
99637842 9963784 Pain

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
99637842 9963784 1 20130201 0