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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126262192 | 12626219 | 2 | F | 20160805 | 20160805 | 20160819 | EXP | 00369797 | CA-HQ SPECIALTY-CA-2016INT000676 | INTERCHEM | 74.00 | YR | F | Y | 0.00000 | 20160819 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126262192 | 12626219 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | U | 201749 | |||||||||
126262192 | 12626219 | 2 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 0 | |||||||||
126262192 | 12626219 | 3 | SS | ANAKINRA | ANAKINRA | 1 | Unknown | UNK | U | 0 | |||||||||
126262192 | 12626219 | 4 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | UNK | U | 0 | |||||||||
126262192 | 12626219 | 5 | SS | IMURAN | AZATHIOPRINE | 1 | Unknown | UNK | U | 0 | |||||||||
126262192 | 12626219 | 6 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | UNK | U | 0 | ||||||||||
126262192 | 12626219 | 7 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
126262192 | 12626219 | 8 | SS | RITUXAN | RITUXIMAB | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126262192 | 12626219 | 1 | Product used for unknown indication |
126262192 | 12626219 | 2 | Rheumatoid arthritis |
126262192 | 12626219 | 3 | Product used for unknown indication |
126262192 | 12626219 | 4 | Product used for unknown indication |
126262192 | 12626219 | 5 | Product used for unknown indication |
126262192 | 12626219 | 6 | Product used for unknown indication |
126262192 | 12626219 | 7 | Product used for unknown indication |
126262192 | 12626219 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126262192 | 12626219 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126262192 | 12626219 | Rheumatoid arthritis | |
126262192 | 12626219 | Treatment failure |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |