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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 97805133 | 9780513 | 3 | F | 2013 | 20160926 | 20131224 | 20160930 | EXP | US-ABBVIE-13P-163-1135586-00 | ABBVIE | 67.56 | YR | F | Y | 0.00000 | 20160930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 97805133 | 9780513 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | 271902E | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | QOW | |||||
| 97805133 | 9780513 | 2 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 | ||||||||||||
| 97805133 | 9780513 | 3 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 0 | ||||||||||||
| 97805133 | 9780513 | 4 | C | ZETIA | EZETIMIBE | 1 | 0 | ||||||||||||
| 97805133 | 9780513 | 5 | C | CELEBREX | CELECOXIB | 1 | 0 | ||||||||||||
| 97805133 | 9780513 | 6 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 97805133 | 9780513 | 7 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
| 97805133 | 9780513 | 8 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 97805133 | 9780513 | 1 | Rheumatoid arthritis |
| 97805133 | 9780513 | 2 | Product used for unknown indication |
| 97805133 | 9780513 | 3 | Product used for unknown indication |
| 97805133 | 9780513 | 4 | Product used for unknown indication |
| 97805133 | 9780513 | 5 | Product used for unknown indication |
| 97805133 | 9780513 | 6 | Product used for unknown indication |
| 97805133 | 9780513 | 7 | Product used for unknown indication |
| 97805133 | 9780513 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 97805133 | 9780513 | OT |
| 97805133 | 9780513 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 97805133 | 9780513 | Aphasia | |
| 97805133 | 9780513 | Drug dose omission | |
| 97805133 | 9780513 | Gait disturbance | |
| 97805133 | 9780513 | Rheumatoid arthritis | |
| 97805133 | 9780513 | Ruptured cerebral aneurysm |
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 |
|---|---|---|---|---|---|---|
| 97805133 | 9780513 | 1 | 2011 | 20130711 | 0 |