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 |