Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103817171 | 10381717 | 1 | I | 20140718 | 20140807 | 20140813 | 20140813 | EXP | KR-BAYER-2014-118713 | BAYER | 17.00 | YR | T | M | Y | 0.00000 | 20140813 | N | OT | KR | KR |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103817171 | 10381717 | 1 | PS | ULTRAKON 300 | IOPROMIDE | 1 | INTRAVENOUS | UNK, ONE TIME ONLY | D | CE1401 | 20220 | SOLUTION FOR INJECTION | 1X |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 103817171 | 10381717 | 1 | Computerised tomogram |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 103817171 | 10381717 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 103817171 | 10381717 | Blood pressure decreased | |
| 103817171 | 10381717 | Chest discomfort | |
| 103817171 | 10381717 | Nausea | |
| 103817171 | 10381717 | Sneezing | |
| 103817171 | 10381717 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 103817171 | 10381717 | 1 | 20140716 | 20140716 | 0 |