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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119847472 | 11984747 | 2 | F | 201506 | 20160704 | 20160201 | 20160712 | EXP | BR-ABBVIE-16K-020-1546238-00 | ABBVIE | 57.98 | YR | F | Y | 86.00000 | KG | 20160712 | CN | COUNTRY NOT SPECIFIED | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119847472 | 11984747 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | 59133XH01 | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||
| 119847472 | 11984747 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | 59133XH01 | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||
| 119847472 | 11984747 | 3 | C | DEPAKENE | VALPROIC ACID | 1 | Oral | 0 | TABLET | ||||||||||
| 119847472 | 11984747 | 4 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | 0 | 8 | DF | TABLET | /wk | |||||||
| 119847472 | 11984747 | 5 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 0 | TABLET | ||||||||||
| 119847472 | 11984747 | 6 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 0 | 3 | GTT | ORAL DROPS | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119847472 | 11984747 | 1 | Rheumatoid arthritis |
| 119847472 | 11984747 | 3 | Seizure |
| 119847472 | 11984747 | 4 | Arthritis |
| 119847472 | 11984747 | 5 | Bone disorder |
| 119847472 | 11984747 | 6 | Vitamin D deficiency |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119847472 | 11984747 | HO |
| 119847472 | 11984747 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119847472 | 11984747 | Dizziness | |
| 119847472 | 11984747 | Head discomfort | |
| 119847472 | 11984747 | Headache | |
| 119847472 | 11984747 | Labyrinthitis | |
| 119847472 | 11984747 | Malaise | |
| 119847472 | 11984747 | Seizure |
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 |
|---|---|---|---|---|---|---|
| 119847472 | 11984747 | 1 | 20130101 | 201509 | 0 | |
| 119847472 | 11984747 | 3 | 2011 | 0 | ||
| 119847472 | 11984747 | 4 | 2010 | 0 | ||
| 119847472 | 11984747 | 6 | 2010 | 0 |