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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5208342 | 6359480 | I | 5208342-7 | 20070104 | 20070110 | DIR | M | N | 9.5 | KG | 20070109 | OT | 20070104 | N | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5208342 | 1008041817 | PS | CEFOTAXIME SODIUM | 1 | INTRAVENOUS | 500 MG Q8 HOUR IV | D | D | |||
| 5208342 | 1008064762 | SS | VINCRISTINE | 1 | INTRAVENOUS | 0.5 MG X1 IV | D | D | |||
| 5208342 | 1008064763 | C | FILGRASTIM | 2 | |||||||
| 5208342 | 1008064764 | C | NYSTATIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5208342 | 1008041817 | ESCHERICHIA INFECTION |
| 5208342 | 1008064762 | MEDULLOBLASTOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5208342 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5208342 | CARDIO-RESPIRATORY ARREST |
| 5208342 | CRYING |
| 5208342 | CYANOSIS |
| 5208342 | LOSS OF CONSCIOUSNESS |
| 5208342 | NYSTAGMUS |
| 5208342 | RESPIRATORY RATE INCREASED |
| 5208342 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |