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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472371 | 6431123 | I | 5472371-9 | 20070906 | 20070918 | 20070930 | EXP | GB-BAUSCH-2007BL003426 | BAUSCH + LOMB INCORPORATED | 82 | YR | M | Y | 85 | KG | 20070930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472371 | 1008989707 | PS | PREDNISOLONE SODIUM PHOSPHATE | 1 | ORAL | 040070 | |||||
| 5472371 | 1008989708 | SS | AMITRIPTYLINE HCL | 1 | ORAL | ||||||
| 5472371 | 1008989709 | SS | ASPIRIN | 1 | ORAL | ||||||
| 5472371 | 1008989710 | C | BECONASE | 1 | |||||||
| 5472371 | 1008989711 | C | CITALOPRAM HYDROBROMIDE | 1 | ORAL | ||||||
| 5472371 | 1008989712 | C | LANSOPRAZOLE | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5472371 | 1008989707 | DRUG USE FOR UNKNOWN INDICATION |
| 5472371 | 1008989708 | DRUG USE FOR UNKNOWN INDICATION |
| 5472371 | 1008989709 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5472371 | HO |
| 5472371 | LT |
| 5472371 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5472371 | GASTROINTESTINAL HAEMORRHAGE |
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 |
|---|---|---|---|---|---|
| 5472371 | 1008989707 | 20070809 | |||
| 5472371 | 1008989708 | 20070626 | |||
| 5472371 | 1008989709 | 20070626 | 20070907 | ||
| 5472371 | 1008989711 | 20070711 | |||
| 5472371 | 1008989712 | 20070829 |