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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127676251 | 12767625 | 1 | I | 20160703 | 20160915 | 20160921 | 20160921 | EXP | US-ALLERGAN-1668971US | ALLERGAN | 81.00 | YR | F | Y | 0.00000 | 20160921 | CN | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127676251 | 12767625 | 1 | PS | RESTASIS | CYCLOSPORINE | 1 | Ophthalmic | 2 GTT, BID | 89063 | 50790 | 2 | GTT | EYE DROPS | BID | |||||
| 127676251 | 12767625 | 2 | C | SYSTANE (HYPROMELLOSE 2910 (4000 MPA.S)) | HYPROMELLOSE 2910 (4000 MPA.S) | 1 | Ophthalmic | 6 TIMES DAILY | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127676251 | 12767625 | 1 | Dry eye |
| 127676251 | 12767625 | 2 | Dry eye |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127676251 | 12767625 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127676251 | 12767625 | Dry eye | |
| 127676251 | 12767625 | Intervertebral disc degeneration | |
| 127676251 | 12767625 | Retinal detachment | |
| 127676251 | 12767625 | Visual acuity reduced |
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 |
|---|---|---|---|---|---|---|
| 127676251 | 12767625 | 1 | 2011 | 0 |