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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117619942 | 11761994 | 2 | F | 20140101 | 20160706 | 20151120 | 20160715 | EXP | CA-PFIZER INC-2015241187 | PFIZER | 70.00 | YR | F | Y | 0.00000 | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117619942 | 11761994 | 1 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | N | 0 | |||||||||
| 117619942 | 11761994 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG, WEEKLY | N | 11719 | 25 | MG | /wk | ||||||
| 117619942 | 11761994 | 3 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | N | 0 | TABLET | |||||||||
| 117619942 | 11761994 | 4 | SS | ACTEMRA | TOCILIZUMAB | 1 | UNK | U | 0 | ||||||||||
| 117619942 | 11761994 | 5 | SS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | UNK | N | 0 | ||||||||||
| 117619942 | 11761994 | 6 | SS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | UNK | N | 0 | ||||||||||
| 117619942 | 11761994 | 7 | SS | PREDNISONE. | PREDNISONE | 1 | 7.5 MG, UNK | 0 | 7.5 | MG | |||||||||
| 117619942 | 11761994 | 8 | SS | DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117619942 | 11761994 | 1 | Rheumatoid arthritis |
| 117619942 | 11761994 | 2 | Rheumatoid arthritis |
| 117619942 | 11761994 | 3 | Rheumatoid arthritis |
| 117619942 | 11761994 | 4 | Rheumatoid arthritis |
| 117619942 | 11761994 | 5 | Rheumatoid arthritis |
| 117619942 | 11761994 | 7 | Rheumatoid arthritis |
| 117619942 | 11761994 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117619942 | 11761994 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117619942 | 11761994 | Arthritis | |
| 117619942 | 11761994 | Condition aggravated | |
| 117619942 | 11761994 | Drug ineffective | |
| 117619942 | 11761994 | Drug intolerance | |
| 117619942 | 11761994 | Eye disorder | |
| 117619942 | 11761994 | Eye pain | |
| 117619942 | 11761994 | Fatigue | |
| 117619942 | 11761994 | Glaucoma | |
| 117619942 | 11761994 | Inflammation | |
| 117619942 | 11761994 | Lacrimation increased | |
| 117619942 | 11761994 | Pain | |
| 117619942 | 11761994 | Photophobia | |
| 117619942 | 11761994 | Post procedural complication | |
| 117619942 | 11761994 | Rheumatoid arthritis | |
| 117619942 | 11761994 | Synovitis |
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 |
|---|---|---|---|---|---|---|
| 117619942 | 11761994 | 7 | 2015 | 0 |