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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126160851 | 12616085 | 1 | I | 2007 | 20160721 | 20160802 | 20160802 | EXP | BR-ABBVIE-16K-020-1687031-00 | ABBVIE | 0.00 | F | Y | 60.00000 | KG | 20160802 | CN | BR | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126160851 | 12616085 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | UNKNOWN | 125057 | SOLUTION FOR INJECTION | ||||||||
| 126160851 | 12616085 | 2 | SS | MABTHERA | RITUXIMAB | 1 | Unknown | UNKNOWN | 0 | INFUSION | |||||||||
| 126160851 | 12616085 | 3 | SS | MABTHERA | RITUXIMAB | 1 | Unknown | UNKNOWN | 0 | INFUSION | |||||||||
| 126160851 | 12616085 | 4 | SS | MABTHERA | RITUXIMAB | 1 | Unknown | UNKNOWN | 0 | 1 | DF | INFUSION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126160851 | 12616085 | 1 | Rheumatoid arthritis |
| 126160851 | 12616085 | 2 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126160851 | 12616085 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126160851 | 12616085 | Arthroscopy | |
| 126160851 | 12616085 | Drug ineffective | |
| 126160851 | 12616085 | Gallbladder operation | |
| 126160851 | 12616085 | Joint range of motion decreased | |
| 126160851 | 12616085 | Joint stiffness | |
| 126160851 | 12616085 | Laryngeal oedema | |
| 126160851 | 12616085 | Mobility decreased | |
| 126160851 | 12616085 | Musculoskeletal stiffness | |
| 126160851 | 12616085 | Nodule | |
| 126160851 | 12616085 | Osteoarthritis | |
| 126160851 | 12616085 | Pain in extremity | |
| 126160851 | 12616085 | Peripheral swelling | |
| 126160851 | 12616085 | Post procedural complication | |
| 126160851 | 12616085 | Tendon rupture |
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 |
|---|---|---|---|---|---|---|
| 126160851 | 12616085 | 2 | 2007 | 0 | ||
| 126160851 | 12616085 | 3 | 20100401 | 0 |