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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125942021 | 12594202 | 1 | I | 2013 | 20160713 | 20160726 | 20160726 | EXP | BR-PFIZER INC-2016346132 | PFIZER | 80.00 | YR | F | Y | 70.00000 | KG | 20160726 | OT | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125942021 | 12594202 | 1 | PS | XALATAN | LATANOPROST | 1 | Ophthalmic | 1 DROP IN THE MORNING AND 1 DROP AT NIGHT, IN EACH EYE | U | 20597 | 2 | GTT | EYE DROPS, SOLUTION | BID | |||||
| 125942021 | 12594202 | 2 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125942021 | 12594202 | 1 | Glaucoma |
| 125942021 | 12594202 | 2 | Abdominal discomfort |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125942021 | 12594202 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125942021 | 12594202 | Cerebrovascular accident | |
| 125942021 | 12594202 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |