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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125799521 | 12579952 | 1 | I | 20151209 | 20160721 | 20160721 | EXP | CA-PFIZER INC-3107481 | PFIZER | 60.00 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125799521 | 12579952 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | U | UNK | 11719 | SOLUTION FOR INJECTION | |||||||
| 125799521 | 12579952 | 2 | SS | LEVOFLOXACIN. | LEVOFLOXACIN | 1 | Unknown | UNK | U | UNK | 78577 | SOLUTION FOR INJECTION | |||||||
| 125799521 | 12579952 | 3 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | UNK | U | UNK | 0 | TABLET | |||||||
| 125799521 | 12579952 | 4 | SS | ARTHROTEC | DICLOFENAC SODIUMMISOPROSTOL | 1 | Unknown | UNK | U | UNK | 0 | TABLET | |||||||
| 125799521 | 12579952 | 5 | SS | CECLOR | CEFACLOR | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125799521 | 12579952 | 6 | SS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, FREQ: 1 DAY; INTERVAL: 1. | U | UNK | 0 | 200 | MG | CAPSULE | |||||
| 125799521 | 12579952 | 7 | SS | DEMEROL | MEPERIDINE HYDROCHLORIDE | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125799521 | 12579952 | 8 | SS | FLAGYL | METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125799521 | 12579952 | 9 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | 400 MG, 3 MONTHS | U | UNK | 0 | 400 | MG | SOLUTION FOR INJECTION | |||||
| 125799521 | 12579952 | 10 | SS | LYRICA | PREGABALIN | 1 | Unknown | UNK | U | UNK | 0 | CAPSULE | |||||||
| 125799521 | 12579952 | 11 | SS | PLAQUENIL /00072602/ | HYDROXYCHLOROQUINE DIPHOSPHATE | 1 | Oral | 400 MG, FREQ: 1 DAY; INTERVAL: 1. | U | UNK | 0 | 400 | MG | TABLET | |||||
| 125799521 | 12579952 | 12 | SS | BISOPROLOL FUMARATE. | BISOPROLOL FUMARATE | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125799521 | 12579952 | 13 | SS | ERYTHROMYCIN. | ERYTHROMYCIN | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125799521 | 12579952 | 14 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | UNK | U | UNK | 0 | TABLET | |||||||
| 125799521 | 12579952 | 15 | SS | NORFLOXACIN | NORFLOXACIN | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125799521 | 12579952 | 16 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | U | UNK | 0 | ||||||||
| 125799521 | 12579952 | 17 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | UNK | U | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125799521 | 12579952 | 1 | Rheumatoid arthritis |
| 125799521 | 12579952 | 2 | Product used for unknown indication |
| 125799521 | 12579952 | 3 | Rheumatoid arthritis |
| 125799521 | 12579952 | 4 | Rheumatoid arthritis |
| 125799521 | 12579952 | 5 | Product used for unknown indication |
| 125799521 | 12579952 | 6 | Product used for unknown indication |
| 125799521 | 12579952 | 7 | Rheumatoid arthritis |
| 125799521 | 12579952 | 8 | Product used for unknown indication |
| 125799521 | 12579952 | 9 | Rheumatoid arthritis |
| 125799521 | 12579952 | 10 | Product used for unknown indication |
| 125799521 | 12579952 | 11 | Rheumatoid arthritis |
| 125799521 | 12579952 | 12 | Product used for unknown indication |
| 125799521 | 12579952 | 13 | Product used for unknown indication |
| 125799521 | 12579952 | 14 | Product used for unknown indication |
| 125799521 | 12579952 | 15 | Product used for unknown indication |
| 125799521 | 12579952 | 16 | Rheumatoid arthritis |
| 125799521 | 12579952 | 17 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125799521 | 12579952 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125799521 | 12579952 | Drug effect incomplete | |
| 125799521 | 12579952 | Drug hypersensitivity | |
| 125799521 | 12579952 | Drug intolerance | |
| 125799521 | 12579952 | Infection | |
| 125799521 | 12579952 | International normalised ratio fluctuation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |