Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630400 | 6555894 | F | 5630400-3 | 20080214 | 20080219 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-14077655 | BRISTOL-MYERS SQUIBB COMPANY | 2 | DY | F | Y | 20080219 | CN | 20071215 | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630400 | 1009532792 | PS | ABILIFY | 1 | TRANSPLACENTAL |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5630400 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5630400 | CEREBRAL HAEMORRHAGE |
| 5630400 | PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5630400 | 1009532792 | 20070423 |