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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126815761 | 12681576 | 1 | I | 20160810 | 20160824 | 20160824 | EXP | AU-HQ SPECIALTY-AU-2016INT000835 | INTERCHEM | 74.00 | YR | F | Y | 0.00000 | 20160824 | MD | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126815761 | 12681576 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 2.1429 MG (15 MG,1 IN 1 W) | 201749 | 15 | MG | ||||||||
| 126815761 | 12681576 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 2.8571 MG (20 MG,1 IN 1 W) | 201749 | 20 | MG | ||||||||
| 126815761 | 12681576 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 1.4286 MG (10 MG,1 IN 1 W) | 201749 | 10 | MG | ||||||||
| 126815761 | 12681576 | 4 | SS | ABATACEPT | ABATACEPT | 1 | Subcutaneous | UNK | 0 | ||||||||||
| 126815761 | 12681576 | 5 | SS | EZETIMIBE. | EZETIMIBE | 1 | Unknown | UNK | 0 | ||||||||||
| 126815761 | 12681576 | 6 | C | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | 400 MG (200 MG,2 IN 1 D) | 0 | 200 | MG | ||||||||
| 126815761 | 12681576 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | 0.7143 MG (5 MG,1 IN 1 W) | U | 0 | 5 | MG | |||||||
| 126815761 | 12681576 | 8 | C | ETANERCEPT | ETANERCEPT | 1 | Unknown | UNK | 0 | ||||||||||
| 126815761 | 12681576 | 9 | SS | TOCILIZUMAB | TOCILIZUMAB | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126815761 | 12681576 | 1 | Rheumatoid arthritis |
| 126815761 | 12681576 | 4 | Product used for unknown indication |
| 126815761 | 12681576 | 5 | Product used for unknown indication |
| 126815761 | 12681576 | 6 | Product used for unknown indication |
| 126815761 | 12681576 | 7 | Product used for unknown indication |
| 126815761 | 12681576 | 8 | Product used for unknown indication |
| 126815761 | 12681576 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126815761 | 12681576 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126815761 | 12681576 | Abdominal distension | |
| 126815761 | 12681576 | Abdominal pain upper | |
| 126815761 | 12681576 | Hepatic cirrhosis | |
| 126815761 | 12681576 | Rheumatoid arthritis |
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 |
|---|---|---|---|---|---|---|
| 126815761 | 12681576 | 1 | 200712 | 0 | ||
| 126815761 | 12681576 | 2 | 201203 | 0 | ||
| 126815761 | 12681576 | 3 | 201205 | 2015 | 0 | |
| 126815761 | 12681576 | 4 | 201209 | 0 | ||
| 126815761 | 12681576 | 6 | 200712 | 201111 | 0 | |
| 126815761 | 12681576 | 7 | 200712 | 0 | ||
| 126815761 | 12681576 | 8 | 200810 | 200902 | 0 | |
| 126815761 | 12681576 | 9 | 201109 | 0 |