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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6250882 | 7037170 | I | 6250882-6 | 20090327 | 20090417 | 20090630 | PER | US-BAUSCH-2009BL001765 | BAUSCH + LOMB INCORPORATED | 45 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6250882 | 1011813147 | PS | ALAWAY | 1 | OPHTHALMIC | 021996 | |||||
6250882 | 1011813148 | C | LOTEMAX | 1 | OPHTHALMIC | ||||||
6250882 | 1011813149 | C | OPTIVE | 2 | OPHTHALMIC |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6250882 | 1011813147 | SEASONAL ALLERGY |
6250882 | 1011813148 | OCULAR HYPERAEMIA |
6250882 | 1011813149 | DRY EYE |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6250882 | EYE HAEMORRHAGE |
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 |
---|---|---|---|---|---|
6250882 | 1011813147 | 20090301 |