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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124331612 | 12433161 | 2 | F | 20160622 | 20160603 | 20160707 | EXP | TR-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-117844 | RANBAXY | 28.00 | YR | F | Y | 0.00000 | 20160707 | OT | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124331612 | 12433161 | 1 | PS | RISPERIDONE. | RISPERIDONE | 1 | Unknown | 1 MG, DAILY | Y | U | 77542 | 1 | MG | ||||||
| 124331612 | 12433161 | 2 | I | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Unknown | 75 MG, DAILY | 0 | 75 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124331612 | 12433161 | 1 | Major depression |
| 124331612 | 12433161 | 2 | Major depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124331612 | 12433161 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124331612 | 12433161 | Drug interaction | |
| 124331612 | 12433161 | Xanthopsia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |