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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6826137 | 7827348 | I | 6826137-5 | 20100521 | 20100708 | DIR | 69 | YR | F | N | 168 | LBS | 20100706 | PH | N | Y | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6826137 | 1014072500 | PS | DORZOLAMIDE HCL AND TIMOLOL MALEATE | 1 | INSTILL 1 DROP IN EACH EYE TWICE A DAY | N | D | 604927 | 20120331 | ||
6826137 | 1014094277 | SS | XALATAN | 1 | |||||||
6826137 | 1014094309 | SS | ALPHAGAN P | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6826137 | 1014072500 | GLAUCOMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6826137 | DS |
6826137 | OT |
Reactions reported
Event ID | PT |
---|---|
6826137 | BLINDNESS |
6826137 | DIARRHOEA |
6826137 | LOSS OF CONSCIOUSNESS |
6826137 | NAUSEA |
6826137 | VOMITING |
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 |
---|---|---|---|---|---|
6826137 | 1014072500 | 20091101 |