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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6699221 | 7368031 | I | 6699221-7 | 20100130 | 20100416 | 20100427 | EXP | GB-TEVA-231816ISR | TEVA | 88 | YR | M | Y | 65 | KG | 20100427 | OT | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6699221 | 1013579877 | PS | BRIMONIDINE | 2 | OPHTHALMIC | 76372 | |||||
6699221 | 1013579878 | SS | DORZOLAMIDE | 1 | OPHTHALMIC | ||||||
6699221 | 1013579879 | SS | ACETYLSALICYLIC ACID | 2 | ORAL | ||||||
6699221 | 1013579880 | SS | FOLIC ACID | 1 | ORAL | ||||||
6699221 | 1013579881 | SS | GANFORT (BIMATOPROST, TIMOLOL) | 2 | OPHTHALMIC | ||||||
6699221 | 1013579882 | SS | MOVICOL | 2 | ORAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6699221 | 1013579877 | GLAUCOMA |
6699221 | 1013579878 | GLAUCOMA |
6699221 | 1013579879 | ATRIAL FIBRILLATION |
6699221 | 1013579880 | ANAEMIA |
6699221 | 1013579881 | GLAUCOMA |
6699221 | 1013579882 | CONSTIPATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6699221 | OT |
Reactions reported
Event ID | PT |
---|---|
6699221 | NEPHROPATHY TOXIC |
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 |
---|---|---|---|---|---|
6699221 | 1013579877 | 20051019 | |||
6699221 | 1013579878 | 20041101 | |||
6699221 | 1013579879 | 20011116 | |||
6699221 | 1013579880 | 20040604 | |||
6699221 | 1013579881 | 20080919 | |||
6699221 | 1013579882 | 20051013 |