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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7047487 | 7959000 | F | 7047487-6 | 20100501 | 20101004 | 20101015 | EXP | DE-ALLERGAN-1012007US | ALLERGANFDA | 64 | YR | F | Y | 63 | KG | 20101015 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7047487 | 1014911240 | PS | BIMATOPROST | 1 | OPHTHALMIC | 1 GTT, QD |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7047487 | 1014911240 | OCULAR HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7047487 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7047487 | CHRONIC OBSTRUCTIVE PULMONARY DISEASE |
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 |
|---|---|---|---|---|---|
| 7047487 | 1014911240 | 20100427 | 20100503 | 7 | DAY |