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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5741479 | 6642655 | I | 5741479-2 | 20060101 | 20070130 | 20080519 | PER | US-BAYER-US-2007-003045 | BAYER HEALTHCARE PHARMACEUTICALS INC. | 30 | YR | M | Y | 20070130 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5741479 | 1009921891 | PS | ULTRAVIST 300 | 1 | INTRAVENOUS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5741479 | 1009921891 | COMPUTERISED TOMOGRAM ABDOMEN |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5741479 | URTICARIA |
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 |
|---|---|---|---|---|---|
| 5741479 | 1009921891 | 20060101 | 20060101 |