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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125705641 | 12570564 | 1 | I | 20160711 | 20160719 | 20160719 | EXP | CA-ABBVIE-16K-028-1675426-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160719 | OT | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125705641 | 12570564 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | UNKNOWN | 125057 | SOLUTION FOR INJECTION | ||||||||
| 125705641 | 12570564 | 2 | SS | ACETYLSALICYLIC ACID | ASPIRIN | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 125705641 | 12570564 | 3 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | U | UNKNOWN | 0 | TABLET | ||||||||
| 125705641 | 12570564 | 4 | SS | DICLOFENAC | DICLOFENAC | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 125705641 | 12570564 | 5 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | U | UNKNOWN | 0 | SOLUTION FOR INJECTION | ||||||||
| 125705641 | 12570564 | 6 | SS | GOLD | GOLD | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 125705641 | 12570564 | 7 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 125705641 | 12570564 | 8 | SS | MOTRIN | IBUPROFEN | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 125705641 | 12570564 | 9 | SS | NAPROSYN | NAPROXEN | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 125705641 | 12570564 | 10 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | U | UNKNOWN | 0 | TABLET | ||||||||
| 125705641 | 12570564 | 11 | C | TRAMADOL. | TRAMADOL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125705641 | 12570564 | 1 | Rheumatoid arthritis |
| 125705641 | 12570564 | 2 | Rheumatoid arthritis |
| 125705641 | 12570564 | 3 | Rheumatoid arthritis |
| 125705641 | 12570564 | 4 | Rheumatoid arthritis |
| 125705641 | 12570564 | 5 | Rheumatoid arthritis |
| 125705641 | 12570564 | 6 | Rheumatoid arthritis |
| 125705641 | 12570564 | 7 | Rheumatoid arthritis |
| 125705641 | 12570564 | 8 | Rheumatoid arthritis |
| 125705641 | 12570564 | 9 | Rheumatoid arthritis |
| 125705641 | 12570564 | 10 | Rheumatoid arthritis |
| 125705641 | 12570564 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125705641 | 12570564 | OT |
| 125705641 | 12570564 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125705641 | 12570564 | Deafness transitory | |
| 125705641 | 12570564 | Decreased appetite | |
| 125705641 | 12570564 | Dizziness | |
| 125705641 | 12570564 | Ear infection | |
| 125705641 | 12570564 | Foot operation | |
| 125705641 | 12570564 | Gastrointestinal pain | |
| 125705641 | 12570564 | Headache | |
| 125705641 | 12570564 | Hypophagia | |
| 125705641 | 12570564 | Nausea | |
| 125705641 | 12570564 | Pharyngitis | |
| 125705641 | 12570564 | Shoulder arthroplasty | |
| 125705641 | 12570564 | Vomiting | |
| 125705641 | 12570564 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |