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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7115782 | 7678060 | I | 7115782-8 | 20101010 | 20101116 | 20101122 | EXP | IT-BAYER-201047113GPV | BAYER HEALTHCARE LLC | 74 | YR | M | Y | 20101122 | MD | ITALY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7115782 | 1015161757 | PS | ASPIRIN | 1 | ORAL | TOTAL DAILY DOSE: 100 MG | 021317 | ||||
| 7115782 | 1015161758 | C | PRIMESIN | 2 | |||||||
| 7115782 | 1015161759 | C | TRIATEC | 2 | |||||||
| 7115782 | 1015161760 | C | PROPAFENONE HCL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7115782 | 1015161757 | THROMBOSIS PROPHYLAXIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7115782 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 7115782 | CEREBRAL HAEMORRHAGE |
| 7115782 | ISCHAEMIC STROKE |
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 |
|---|---|---|---|---|---|
| 7115782 | 1015161757 | 20001001 | 20101010 | 3663 | DAY |