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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127902021 | 12790202 | 1 | I | 201608 | 20160926 | 20160928 | 20160928 | EXP | US-ABBVIE-16K-163-1739573-00 | ABBVIE | 57.90 | YR | M | Y | 0.00000 | 20160928 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127902021 | 12790202 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | QOW | |||||
127902021 | 12790202 | 2 | SS | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127902021 | 12790202 | 1 | Crohn's disease |
127902021 | 12790202 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127902021 | 12790202 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127902021 | 12790202 | Coronary artery occlusion | |
127902021 | 12790202 | Drug ineffective | |
127902021 | 12790202 | Electrocardiogram abnormal | |
127902021 | 12790202 | Vascular stent occlusion |
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 |
---|---|---|---|---|---|---|
127902021 | 12790202 | 1 | 2015 | 0 |