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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125297991 | 12529799 | 1 | I | 20160624 | 20160706 | 20160706 | EXP | BR-BAUSCH-BL-2016-015422 | BAUSCH AND LOMB | 39.00 | YR | F | Y | 60.00000 | KG | 20160706 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125297991 | 12529799 | 1 | PS | WELLBUTRIN XL | BUPROPION HYDROCHLORIDE | 1 | Oral | Y | 15K012 | 21515 | 1 | DF | TABLET | QD | |||||
| 125297991 | 12529799 | 2 | SS | WELLBUTRIN SR | BUPROPION HYDROCHLORIDE | 1 | Oral | Y | 0 | 1 | DF | PROLONGED-RELEASE TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125297991 | 12529799 | 1 | Depression |
| 125297991 | 12529799 | 2 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125297991 | 12529799 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125297991 | 12529799 | Agitation | |
| 125297991 | 12529799 | Arrhythmia | |
| 125297991 | 12529799 | Incorrect dose administered | |
| 125297991 | 12529799 | Nervousness | |
| 125297991 | 12529799 | Product availability issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |