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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126919201 | 12691920 | 1 | I | 20160822 | 20160827 | 20160827 | EXP | CA-AMGEN-CANSP2016110405 | AMGEN | 61.00 | YR | A | M | Y | 0.00000 | 20160827 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126919201 | 12691920 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, QWK | U | 103795 | 50 | MG | UNKNOWN FORMULATION | /wk | |||||
| 126919201 | 12691920 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 10 MG, QWK | 0 | 10 | MG | /wk | |||||||
| 126919201 | 12691920 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG, QWK | 0 | 25 | MG | /wk | |||||||
| 126919201 | 12691920 | 4 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | 200 MG, UNK | 0 | 200 | MG | ||||||||
| 126919201 | 12691920 | 5 | SS | VIOXX | ROFECOXIB | 1 | Unknown | 12.5 MG, QD | 0 | 12.5 | MG | TABLET | QD | ||||||
| 126919201 | 12691920 | 6 | C | MOBICOX | MELOXICAM | 1 | Oral | UNK UNK, QD | 0 | TABLET | QD | ||||||||
| 126919201 | 12691920 | 7 | C | MOTRIN | IBUPROFEN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126919201 | 12691920 | 1 | Ankylosing spondylitis |
| 126919201 | 12691920 | 2 | Product used for unknown indication |
| 126919201 | 12691920 | 4 | Product used for unknown indication |
| 126919201 | 12691920 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126919201 | 12691920 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126919201 | 12691920 | Drug ineffective | |
| 126919201 | 12691920 | Hypertension | |
| 126919201 | 12691920 | Iritis | |
| 126919201 | 12691920 | Nervous system disorder | |
| 126919201 | 12691920 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |