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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123838672 | 12383867 | 2 | F | 20160825 | 20160519 | 20160902 | EXP | PE-PFIZER INC-2016257804 | PFIZER | 84.00 | YR | M | Y | 0.00000 | 20160902 | CN | PE | PE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123838672 | 12383867 | 1 | PS | XALATAN | LATANOPROST | 1 | Ophthalmic | 1 GTT ON EACH EYE, DAILY | M35119-L55635 | 20597 | 1 | GTT | EYE DROPS, SOLUTION |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123838672 | 12383867 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123838672 | 12383867 | Blindness unilateral | |
| 123838672 | 12383867 | Drug dose omission | |
| 123838672 | 12383867 | Eye pain | |
| 123838672 | 12383867 | Glaucoma | |
| 123838672 | 12383867 | Headache | |
| 123838672 | 12383867 | Intraocular pressure increased |
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 |
|---|---|---|---|---|---|---|
| 123838672 | 12383867 | 1 | 2011 | 0 |