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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4785959 | 5893940 | I | 4785959-5 | 20050818 | 20050915 | 20050930 | EXP | 2005RR-00756 | 48 | YR | M | N | 20050929 | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4785959 | 1006476350 | PS | ASPIRIN (ASPIRIN, ASPIRIN) UNKNOWN | 2 | ORAL | 75 MG, QD,ORAL | U | U | 6809 | ||
| 4785959 | 1006495609 | SS | IBUPROFEN | 1 | ORAL | 400 MG, Q4H, ORAL | U | U | |||
| 4785959 | 1006495614 | C | DOXAZOSIN | 2 | |||||||
| 4785959 | 1006495615 | C | BENZAFIBRATE | 2 | |||||||
| 4785959 | 1006495619 | C | ALLOPURINOL | 1 | |||||||
| 4785959 | 1006495623 | C | IRBESARTAN AND HYDROCHLOROTHIAZIDE | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4785959 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4785959 | GASTRITIS |
| 4785959 | GASTROINTESTINAL HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4785959 | FGN |
| 4785959 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4785959 | 1006476350 | 20050828 |