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
125663022 12566302 2 F 20160707 20160718 20160719 EXP NZ-ABBVIE-16K-118-1658723-00 ABBVIE 0.00 F Y 55.10000 KG 20160719 MD COUNTRY NOT SPECIFIED NZ

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
125663022 12566302 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 SOLUTION FOR INJECTION
125663022 12566302 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION /wk
125663022 12566302 3 SS INFLIXIMAB INFLIXIMAB 1 Unknown U UNKNOWN 0
125663022 12566302 4 C METHOTREXATE. METHOTREXATE 1 0 TABLET
125663022 12566302 5 C AZATHIOPRINE. AZATHIOPRINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125663022 12566302 1 Crohn's disease
125663022 12566302 3 Product used for unknown indication
125663022 12566302 4 Product used for unknown indication
125663022 12566302 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125663022 12566302 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125663022 12566302 Anaphylactic reaction
125663022 12566302 Drug ineffective
125663022 12566302 Drug level 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
125663022 12566302 1 2011 0