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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5797495 | 6522946 | F | 5 | 5797495-8 | 20070101 | 20080616 | 20080630 | EXP | 8028572 | UCB, INC. | F | N | 20080624 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5797495 | 1010120673 | PS | KEPPRA | 1 | TRANSPLACENTAL | 3000 MG/ D TRP | 21035 | ||||
| 5797495 | 1010152256 | SS | KEPPRA | 1 | TRANSPLACENTAL | 3500 MG /D TRP | |||||
| 5797495 | 1010152258 | C | LAMICTAL | 1 | |||||||
| 5797495 | 1010152259 | C | PROCARDIA | 1 | |||||||
| 5797495 | 1010152260 | C | FOLIC ACID | 1 | |||||||
| 5797495 | 1010152261 | C | VITAMIN TAB | 1 | |||||||
| 5797495 | 1010152262 | C | BETAMETHASONE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5797495 | 1010120673 | CONVULSION |
| 5797495 | 1010152256 | CONVULSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5797495 | CA |
Reactions reported
| Event ID | PT |
|---|---|
| 5797495 | FOETAL GROWTH RETARDATION |
| 5797495 | FOOT DEFORMITY |
| 5797495 | HAEMANGIOMA |
| 5797495 | MATERNAL DRUGS AFFECTING FOETUS |
| 5797495 | PREMATURE BABY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5797495 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5797495 | 1010120673 | 20070101 | 20070816 | ||
| 5797495 | 1010152256 | 20070816 | 20070903 |