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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6250881 | 7037169 | I | 6250881-4 | 20090408 | 20090421 | 20090630 | PER | US-BAUSCH-2009BL001756 | BAUSCH + LOMB INCORPORATED | 87 | YR | M | Y | 88 | KG | 20090630 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6250881 | 1011813141 | PS | ALAWAY | 1 | OPHTHALMIC | A41902 | 021996 | ||||
| 6250881 | 1011813142 | C | ENALAPRIL MALEATE | 1 | ORAL | ||||||
| 6250881 | 1011813143 | C | OMEPRAZOLE | 1 | ORAL | ||||||
| 6250881 | 1011813144 | C | AMLODIPINE BESYLATE | 1 | ORAL | ||||||
| 6250881 | 1011813145 | C | FLOMAX | 1 | ORAL | ||||||
| 6250881 | 1011813146 | C | SIMVASTATIN | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6250881 | 1011813141 | EYE PRURITUS |
| 6250881 | 1011813142 | HYPERTENSION |
| 6250881 | 1011813143 | GASTROOESOPHAGEAL REFLUX DISEASE |
| 6250881 | 1011813144 | HYPERTENSION |
| 6250881 | 1011813145 | PROSTATOMEGALY |
| 6250881 | 1011813146 | BLOOD CHOLESTEROL INCREASED |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6250881 | INSTILLATION SITE IRRITATION |
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 |
|---|---|---|---|---|---|
| 6250881 | 1011813141 | 20090408 | |||
| 6250881 | 1011813144 | 20070101 | |||
| 6250881 | 1011813145 | 20050101 | |||
| 6250881 | 1011813146 | 20070101 |