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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126577031 | 12657703 | 1 | I | 20160808 | 20160816 | 20160816 | PER | US-TAKEDA-2016TUS014148 | TAKEDA | 0.00 | A | Y | 0.00000 | 20160816 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126577031 | 12657703 | 1 | PS | BRINTELLIX | VORTIOXETINE HYDROBROMIDE | 1 | Unknown | UNK | U | UNKNOWN | 204447 | TABLET | |||||||
| 126577031 | 12657703 | 2 | SS | FLEXERIL | CYCLOBENZAPRINE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126577031 | 12657703 | 1 | Product used for unknown indication |
| 126577031 | 12657703 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126577031 | 12657703 | Burning sensation | |
| 126577031 | 12657703 | Chronic fatigue syndrome | |
| 126577031 | 12657703 | Feeling abnormal | |
| 126577031 | 12657703 | Hypoaesthesia | |
| 126577031 | 12657703 | Mitral valve prolapse | |
| 126577031 | 12657703 | Somnolence | |
| 126577031 | 12657703 | Tinnitus | |
| 126577031 | 12657703 | Unhealthy diet |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |