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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5741477 | 6642653 | F | 5741477-9 | 20070130 | 20080519 | PER | US-BAYER-US-2007-002356 | BAYER HEALTHCARE PHARMACEUTICALS INC. | F | Y | 20070130 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5741477 | 1009921889 | PS | ULTRAVIST 300 | 1 | INTRAVENOUS |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5741477 | 1009921889 | COMPUTERISED TOMOGRAM |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5741477 | ACCIDENTAL EXPOSURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |