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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127233901 | 12723390 | 1 | I | 20160819 | 20160906 | 20160908 | 20160908 | EXP | IT-ROCHE-1827213 | ROCHE | 50.78 | YR | F | Y | 0.00000 | 20160908 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127233901 | 12723390 | 1 | PS | CLONAZEPAM. | CLONAZEPAM | 1 | Unknown | U | 17533 | ||||||||||
| 127233901 | 12723390 | 2 | SS | LAMOTRIGINE. | LAMOTRIGINE | 1 | Unknown | U | 0 | ||||||||||
| 127233901 | 12723390 | 3 | SS | RISPERIDONE. | RISPERIDONE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127233901 | 12723390 | 1 | Product used for unknown indication |
| 127233901 | 12723390 | 2 | Product used for unknown indication |
| 127233901 | 12723390 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127233901 | 12723390 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127233901 | 12723390 | Intentional self-injury | |
| 127233901 | 12723390 | Miosis | |
| 127233901 | 12723390 | Sopor | |
| 127233901 | 12723390 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |