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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127614261 | 12761426 | 1 | I | 20160819 | 20160916 | 20160920 | 20160920 | PER | ALCN2016US006430 | ALCON | 63.00 | YR | F | Y | 0.00000 | 20160920 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127614261 | 12761426 | 1 | PS | LATANOPROST. | LATANOPROST | 1 | Ophthalmic | 1 GTT, QD, FOR 18 DAYS | U | UNKNOWN | 91449 | 1 | GTT | QD | |||||
| 127614261 | 12761426 | 2 | C | REFRESH /00880201/ | POLYVINYL ALCOHOLPOVIDONE | 1 | Ophthalmic | UNK UNK, PRN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127614261 | 12761426 | 1 | Glaucoma |
| 127614261 | 12761426 | 2 | Dry eye |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127614261 | 12761426 | Eye irritation | |
| 127614261 | 12761426 | Ocular hyperaemia |
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 |
|---|---|---|---|---|---|---|
| 127614261 | 12761426 | 1 | 20160819 | 0 |