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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480337 | 8644638 | I | 8480337-X | 20120602 | 20120625 | 20120630 | EXP | GB-TEVA-344899ISR | TEVA | 60 | YR | M | Y | 20120630 | MD | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480337 | 1020135267 | PS | PHENYTOIN | 1 | 080259 | ||||||
| 8480337 | 1020135268 | SS | DALTEPARIN SODIUM | 1 | SUBCUTANEOUS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8480337 | 1020135267 | CONVULSION |
| 8480337 | 1020135268 | DEEP VEIN THROMBOSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8480337 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 8480337 | BLISTER |
| 8480337 | SKIN EXFOLIATION |
| 8480337 | RASH MACULO-PAPULAR |
| 8480337 | PAIN |
| 8480337 | DEHYDRATION |
| 8480337 | ORAL DISORDER |
| 8480337 | RESPIRATORY FAILURE |
| 8480337 | APHAGIA |
| 8480337 | EYE DISORDER |
| 8480337 | TOXIC EPIDERMAL NECROLYSIS |
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 |
|---|---|---|---|---|---|
| 8480337 | 1020135267 | 20120401 | |||
| 8480337 | 1020135268 | 20120525 | 20120606 |