Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125918881 | 12591888 | 1 | I | 20160414 | 0 | 20160725 | 20160725 | DIR | 41.00 | YR | M | N | 180.00000 | LBS | 20160722 | Y | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125918881 | 12591888 | 1 | PS | RESTASIS | CYCLOSPORINE | 1 | Ophthalmic | Y | Y | 90602 | 20171101 | 0 | 1 | GTT | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125918881 | 12591888 | 1 | Dry eye |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125918881 | 12591888 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125918881 | 12591888 | Erythema | |
| 125918881 | 12591888 | Eye irritation | |
| 125918881 | 12591888 | Eye pain | |
| 125918881 | 12591888 | Eyelid irritation | |
| 125918881 | 12591888 | Eyelid pain | |
| 125918881 | 12591888 | Ocular hyperaemia | |
| 125918881 | 12591888 | Skin irritation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125918881 | 12591888 | 1 | 20160617 | 0 |