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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6822818 | 7827346 | I | 6822818-8 | 20100413 | 20100706 | DIR | 63 | YR | M | N | 250 | LBS | 20100702 | MD | N | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6822818 | 1014059081 | PS | DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | 1 | OPHTHALMIC | 1 DROP BID OPHTHALMIC | Y | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6822818 | 1014059081 | GLAUCOMA |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6822818 | EYE IRRITATION |
| 6822818 | OCULAR HYPERAEMIA |
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 |
|---|---|---|---|---|---|
| 6822818 | 1014059081 | 20091019 | 20100402 | 6 | MON |