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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124888473 | 12488847 | 3 | F | 201605 | 20160728 | 20160622 | 20160805 | EXP | RU-PFIZER INC-2016296090 | PFIZER | 77.00 | YR | F | Y | 0.00000 | 20160805 | OT | RU | RU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124888473 | 12488847 | 1 | PS | XALATAN | LATANOPROST | 1 | Ophthalmic | 1 DROP, 1X/DAY | Y | 20597 | 1 | DF | EYE DROPS, SOLUTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124888473 | 12488847 | 1 | Glaucoma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124888473 | 12488847 | HO |
| 124888473 | 12488847 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124888473 | 12488847 | Eye oedema | |
| 124888473 | 12488847 | Eye pain | |
| 124888473 | 12488847 | Intraocular pressure increased | |
| 124888473 | 12488847 | Ocular hyperaemia | |
| 124888473 | 12488847 | Product quality issue |
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 |
|---|---|---|---|---|---|---|
| 124888473 | 12488847 | 1 | 201605 | 20160504 | 0 |