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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5977617 | 6831170 | I | 5977617-6 | 20081001 | 20081001 | 20081203 | EXP | AT-MERCK-0811AUT00009 | MERCK HUMAN HEALTH DIVISION | F | Y | 20081203 | MD | AUSTRIA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5977617 | 1010791141 | PS | DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | 1 | OPHTHALMIC | 20869 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5977617 | 1010791141 | GLAUCOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5977617 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5977617 | AMNESIA |
| 5977617 | CONFUSIONAL STATE |
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 |
|---|---|---|---|---|---|
| 5977617 | 1010791141 | 20080101 | 20081001 |