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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6250879 | 7037167 | I | 6250879-6 | 20090329 | 20090331 | 20090630 | PER | US-BAUSCH-2009BL001447 | BAUSCH + LOMB INCORPORATED | 60 | YR | F | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6250879 | 1011813132 | PS | ALAWAY | 1 | OPHTHALMIC | A27073 | 021996 | ||||
| 6250879 | 1011813133 | C | CLARITIN /USA/ | 2 | |||||||
| 6250879 | 1011813134 | C | IMITREX ^CERENEX^ | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6250879 | 1011813132 | EYE PRURITUS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6250879 | 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 |
|---|---|---|---|---|---|
| 6250879 | 1011813132 | 20090329 | 20090329 |