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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127181041 | 12718104 | 1 | I | 2015 | 20151223 | 20160906 | 20160906 | EXP | CA-PFIZER INC-2015472901 | PFIZER | 59.00 | YR | F | Y | 0.00000 | 20160906 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127181041 | 12718104 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | 25 MG, WEEKLY | 11719 | 25 | MG | /wk | ||||||||
| 127181041 | 12718104 | 2 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | 1 G, 2X/DAY | N | 7073 | 1 | G | BID | |||||||
| 127181041 | 12718104 | 3 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 400 MG, 1X/DAY | 0 | 400 | MG | QD | ||||||||
| 127181041 | 12718104 | 4 | SS | SIMPONI | GOLIMUMAB | 1 | 50 MG, MONTHLY | N | 0 | 50 | MG | /month | |||||||
| 127181041 | 12718104 | 5 | SS | PREDNISONE. | PREDNISONE | 1 | 10 MG, 1X/DAY | 0 | 10 | MG | QD | ||||||||
| 127181041 | 12718104 | 6 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | 20 MG, 1X/DAY | N | 0 | 20 | MG | QD | |||||||
| 127181041 | 12718104 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | UNK | 0 | |||||||||||
| 127181041 | 12718104 | 8 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127181041 | 12718104 | 1 | Rheumatoid arthritis |
| 127181041 | 12718104 | 2 | Rheumatoid arthritis |
| 127181041 | 12718104 | 3 | Rheumatoid arthritis |
| 127181041 | 12718104 | 4 | Rheumatoid arthritis |
| 127181041 | 12718104 | 5 | Rheumatoid arthritis |
| 127181041 | 12718104 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127181041 | 12718104 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127181041 | 12718104 | Condition aggravated | |
| 127181041 | 12718104 | Diarrhoea | |
| 127181041 | 12718104 | Drug effect incomplete | |
| 127181041 | 12718104 | Drug intolerance | |
| 127181041 | 12718104 | Fatigue | |
| 127181041 | 12718104 | Feeling abnormal | |
| 127181041 | 12718104 | Headache | |
| 127181041 | 12718104 | Insomnia | |
| 127181041 | 12718104 | Rheumatoid arthritis | |
| 127181041 | 12718104 | Sinusitis | |
| 127181041 | 12718104 | Stress | |
| 127181041 | 12718104 | Tinnitus |
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 |
|---|---|---|---|---|---|---|
| 127181041 | 12718104 | 1 | 20130801 | 0 | ||
| 127181041 | 12718104 | 2 | 20130930 | 20131113 | 0 | |
| 127181041 | 12718104 | 3 | 20131113 | 0 | ||
| 127181041 | 12718104 | 4 | 20150414 | 20151214 | 0 | |
| 127181041 | 12718104 | 5 | 20130801 | 0 | ||
| 127181041 | 12718104 | 6 | 20150227 | 20150316 | 0 |