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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126268381 | 12626838 | 1 | I | 20160802 | 20160805 | 20160805 | EXP | TR-JNJFOC-20160801731 | JANSSEN | ZEYDAN B, UYGUNOGLU U, SAIP S, DEMIRCI ON, SEYAHI E, UGURLU S, ET AL. INFLIXIMAB IS A PLAUSIBLE ALTERNATIVE FOR NEUROLOGIC COMPLICATIONS OF BEH?ET DISEASE. NEUROLOGY NEUROIMMUNOLOGY + NEUROINFLAMMATION 2016;3 (5):1-9. | 0.00 | Y | 0.00000 | 20160805 | MD | TR | TR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126268381 | 12626838 | 1 | PS | INFLIXIMAB, RECOMBINANT | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | AT WEEKS 0, 2, AND 6, THEN ONCE EVERY 8 WEEKS. | U | 103772 | 5 | MG/KG | LYOPHILIZED POWDER |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126268381 | 12626838 | 1 | Behcet's syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126268381 | 12626838 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126268381 | 12626838 | Off label use | |
| 126268381 | 12626838 | Product use issue | |
| 126268381 | 12626838 | Pulmonary tuberculosis | |
| 126268381 | 12626838 | Tuberculosis of central nervous system |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |