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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8359258 | 8563494 | I | 8359258-9 | 20110801 | 20110822 | 20111004 | PER | 2011IP000152 | ISTA PHARMACEUTICALS, INC. | YR | M | N | 20110919 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8359258 | 1019691600 | PS | BEPREVE | 1 | ORAL | ; OPH | 022288 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8359258 | 1019691600 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 8359258 | DECREASED APPETITE |
| 8359258 | ABDOMINAL DISCOMFORT |
| 8359258 | HYPERHIDROSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 8359258 | CSM |
Therapies reported
| no results found |