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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120367532 | 12036753 | 2 | F | 20160815 | 20160208 | 20160822 | EXP | GB-ABBVIE-16K-167-1552445-00 | ABBVIE | 0.00 | M | Y | 96.00000 | KG | 20160822 | OT | COUNTRY NOT SPECIFIED | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120367532 | 12036753 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | UNKNOWN | 125057 | 40 | MG | INJECTION | QOW | |||||
| 120367532 | 12036753 | 2 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120367532 | 12036753 | 1 | Psoriasis |
| 120367532 | 12036753 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120367532 | 12036753 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120367532 | 12036753 | Chest pain | |
| 120367532 | 12036753 | Dizziness | |
| 120367532 | 12036753 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 120367532 | 12036753 | 1 | 20120425 | 20151104 | 0 | |
| 120367532 | 12036753 | 2 | 20110323 | 0 |