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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120001832 | 12000183 | 2 | F | 20160127 | 20160204 | 20160912 | PER | US-APOTEX-2015AP014761 | APOTEX | 52.00 | YR | M | Y | 0.00000 | 20160912 | CN | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120001832 | 12000183 | 1 | PS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 40 MG, QD | U | U | 75356 | 40 | MG | TABLET | |||||
| 120001832 | 12000183 | 2 | I | LOXAPINE. | LOXAPINE | 1 | Unknown | 5 MG DAILY FOR 2.4 YEARS | U | U | 0 | 5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120001832 | 12000183 | 1 | Prader-Willi syndrome |
| 120001832 | 12000183 | 2 | Prader-Willi syndrome |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120001832 | 12000183 | Drug interaction | |
| 120001832 | 12000183 | Tardive dyskinesia | |
| 120001832 | 12000183 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |