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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 104211822 | 10421182 | 2 | F | 20140526 | 20160722 | 20140830 | 20160729 | EXP | BR-AMGEN-BRASP2014065670 | AMGEN | 55.00 | YR | A | M | Y | 68.00000 | KG | 20160729 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 104211822 | 10421182 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, ONCE WEEKLY | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | ||||||
| 104211822 | 10421182 | 2 | SS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, WEEKLY | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | ||||||
| 104211822 | 10421182 | 3 | C | ALIVIUM | 2 | 600 MG, AS NECESSARY | 0 | 600 | MG | ||||||||||
| 104211822 | 10421182 | 4 | C | TRAMAL | TRAMADOL | 1 | UNK UNK, AS NECESSARY | 0 | |||||||||||
| 104211822 | 10421182 | 5 | C | TRAMAL | TRAMADOL | 1 | UNK, AS NEEDED | 0 | |||||||||||
| 104211822 | 10421182 | 6 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 104211822 | 10421182 | 7 | C | METHOTREXATE. | METHOTREXATE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 104211822 | 10421182 | 1 | Ankylosing spondylitis |
| 104211822 | 10421182 | 3 | Pain |
| 104211822 | 10421182 | 4 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 104211822 | 10421182 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 104211822 | 10421182 | Abasia | |
| 104211822 | 10421182 | Arthralgia | |
| 104211822 | 10421182 | Arthropathy | |
| 104211822 | 10421182 | Diarrhoea | |
| 104211822 | 10421182 | Ear infection | |
| 104211822 | 10421182 | Fungal infection | |
| 104211822 | 10421182 | Malaise | |
| 104211822 | 10421182 | Mobility decreased | |
| 104211822 | 10421182 | Muscular weakness | |
| 104211822 | 10421182 | Nausea | |
| 104211822 | 10421182 | Pallor | |
| 104211822 | 10421182 | Pollakiuria | |
| 104211822 | 10421182 | Pyrexia | |
| 104211822 | 10421182 | Rotator cuff syndrome | |
| 104211822 | 10421182 | Urinary tract infection |
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 |
|---|---|---|---|---|---|---|
| 104211822 | 10421182 | 1 | 201309 | 201404 | 0 | |
| 104211822 | 10421182 | 2 | 2014 | 0 | ||
| 104211822 | 10421182 | 3 | 201406 | 0 | ||
| 104211822 | 10421182 | 7 | 2005 | 0 |