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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125808911 | 12580891 | 1 | I | 2010 | 20151109 | 20160721 | 20160721 | EXP | CA-PFIZER INC-2015386106 | PFIZER | 77.00 | YR | F | Y | 0.00000 | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125808911 | 12580891 | 1 | SS | ENBREL | ETANERCEPT | 1 | UNK | N | 0 | ||||||||||
| 125808911 | 12580891 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | UNK | N | 11719 | ||||||||||
| 125808911 | 12580891 | 3 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | 400 MG, UNK | N | 0 | 400 | MG | ||||||||
| 125808911 | 12580891 | 4 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | 10-20MG | N | 0 | ||||||||||
| 125808911 | 12580891 | 5 | SS | HUMIRA | ADALIMUMAB | 1 | UNK | U | 0 | ||||||||||
| 125808911 | 12580891 | 6 | SS | ORENCIA | ABATACEPT | 1 | Subcutaneous | 125 MG, UNK | N | 0 | 125 | MG | |||||||
| 125808911 | 12580891 | 7 | SS | PROLIA | DENOSUMAB | 1 | UNK | U | 0 | ||||||||||
| 125808911 | 12580891 | 8 | C | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125808911 | 12580891 | 1 | Rheumatoid arthritis |
| 125808911 | 12580891 | 2 | Rheumatoid arthritis |
| 125808911 | 12580891 | 3 | Rheumatoid arthritis |
| 125808911 | 12580891 | 4 | Rheumatoid arthritis |
| 125808911 | 12580891 | 5 | Rheumatoid arthritis |
| 125808911 | 12580891 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125808911 | 12580891 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125808911 | 12580891 | Abdominal pain | |
| 125808911 | 12580891 | Aggression | |
| 125808911 | 12580891 | Alopecia | |
| 125808911 | 12580891 | Asthenia | |
| 125808911 | 12580891 | Blood creatinine increased | |
| 125808911 | 12580891 | Cough | |
| 125808911 | 12580891 | Diarrhoea | |
| 125808911 | 12580891 | Drug ineffective | |
| 125808911 | 12580891 | Drug intolerance | |
| 125808911 | 12580891 | Dyspnoea | |
| 125808911 | 12580891 | Increased upper airway secretion | |
| 125808911 | 12580891 | Lung disorder | |
| 125808911 | 12580891 | Peripheral swelling | |
| 125808911 | 12580891 | Retinopathy | |
| 125808911 | 12580891 | Sinus disorder | |
| 125808911 | 12580891 | Sinusitis | |
| 125808911 | 12580891 | Tachyphylaxis | |
| 125808911 | 12580891 | 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 |
|---|---|---|---|---|---|---|
| 125808911 | 12580891 | 1 | 20110707 | 201402 | 0 | |
| 125808911 | 12580891 | 2 | 20101001 | 20101201 | 0 | |
| 125808911 | 12580891 | 4 | 20110201 | 20110401 | 0 | |
| 125808911 | 12580891 | 5 | 2015 | 0 | ||
| 125808911 | 12580891 | 6 | 20140429 | 20141218 | 0 | |
| 125808911 | 12580891 | 7 | 201501 | 0 |