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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125424053 | 12542405 | 3 | F | 20160523 | 20160824 | 20160708 | 20160826 | EXP | ALCN2016US004562 | ALCON | 89.00 | YR | M | Y | 111.11000 | KG | 20160826 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125424053 | 12542405 | 1 | PS | LATANOPROST. | LATANOPROST | 1 | Ophthalmic | UNK GTT, QHS | Y | N | 261101F | 91449 | |||||||
125424053 | 12542405 | 2 | C | ADVIL | IBUPROFEN | 1 | Unknown | U | 0 | ||||||||||
125424053 | 12542405 | 3 | C | CLARITIN-D 12 HOUR | LORATADINEPSEUDOEPHEDRINE SULFATE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125424053 | 12542405 | 1 | Intraocular pressure increased |
125424053 | 12542405 | 2 | Product used for unknown indication |
125424053 | 12542405 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125424053 | 12542405 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125424053 | 12542405 | Blindness transient | |
125424053 | 12542405 | Vision blurred |
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 |
---|---|---|---|---|---|---|
125424053 | 12542405 | 1 | 20160523 | 20160624 | 0 |