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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124473732 | 12447373 | 2 | F | 20160711 | 20160608 | 20160722 | EXP | AU-PFIZER INC-2016281910 | PFIZER | 89.00 | YR | F | Y | 0.00000 | 20160722 | CN | AU | AU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124473732 | 12447373 | 1 | PS | XALATAN | LATANOPROST | 1 | Ophthalmic | 1 GTT, 1X/DAY | U | M70341 | 20597 | 1 | GTT | EYE DROPS, SOLUTION | QD | ||||
124473732 | 12447373 | 2 | C | LUCENTIS | RANIBIZUMAB | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124473732 | 12447373 | 1 | Intraocular pressure increased |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124473732 | 12447373 | HO |
124473732 | 12447373 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124473732 | 12447373 | Eye irritation | |
124473732 | 12447373 | Incorrect dose administered | |
124473732 | 12447373 | Joint range of motion decreased | |
124473732 | 12447373 | Product dropper 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 |
---|---|---|---|---|---|---|
124473732 | 12447373 | 1 | 201007 | 0 | ||
124473732 | 12447373 | 2 | 20150423 | 0 |