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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127648981 | 12764898 | 1 | I | 20160914 | 20160921 | 20160921 | EXP | CA-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-076287 | BRISTOL MYERS SQUIBB | 0.00 | F | Y | 0.00000 | 20160921 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127648981 | 12764898 | 1 | PS | ORENCIA | ABATACEPT | 1 | Unknown | UNK | U | 125118 | |||||||||
| 127648981 | 12764898 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | U | 0 | |||||||||
| 127648981 | 12764898 | 3 | SS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Unknown | UNK | U | 0 | |||||||||
| 127648981 | 12764898 | 4 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 0 | |||||||||
| 127648981 | 12764898 | 5 | C | METHOTREXATE. | METHOTREXATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127648981 | 12764898 | 6 | C | PLAQUENIL /00072602/ | HYDROXYCHLOROQUINE DIPHOSPHATE | 1 | Unknown | UNK | U | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127648981 | 12764898 | 1 | Product used for unknown indication |
| 127648981 | 12764898 | 2 | Product used for unknown indication |
| 127648981 | 12764898 | 3 | Product used for unknown indication |
| 127648981 | 12764898 | 4 | Product used for unknown indication |
| 127648981 | 12764898 | 5 | Product used for unknown indication |
| 127648981 | 12764898 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127648981 | 12764898 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127648981 | 12764898 | Arthralgia | |
| 127648981 | 12764898 | Drug ineffective | |
| 127648981 | 12764898 | Hypersensitivity | |
| 127648981 | 12764898 | Joint range of motion decreased | |
| 127648981 | 12764898 | Joint swelling | |
| 127648981 | 12764898 | Musculoskeletal pain | |
| 127648981 | 12764898 | Musculoskeletal stiffness | |
| 127648981 | 12764898 | Peripheral swelling | |
| 127648981 | 12764898 | Tendon disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |