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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127844871 | 12784487 | 1 | I | 20070511 | 20091230 | 20160927 | 20160927 | EXP | GB-PFIZER INC-473799 | PFIZER | 81.00 | YR | F | Y | 0.00000 | 20160927 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127844871 | 12784487 | 1 | PS | VANCOMYCIN HCL | VANCOMYCIN HYDROCHLORIDE | 1 | Intraocular | 10 MG, UNK | N | 62911 | 10 | MG | POWDER FOR INJECTION | ||||||
127844871 | 12784487 | 2 | SS | VANCOMYCIN HCL | VANCOMYCIN HYDROCHLORIDE | 1 | N | 62911 | POWDER FOR INJECTION | ||||||||||
127844871 | 12784487 | 3 | SS | ADRENALINE /00003901/ | EPINEPHRINE | 1 | Intraocular | 0.3 ML, UNK | N | 0 | .3 | ML | |||||||
127844871 | 12784487 | 4 | SS | ADRENALINE /00003901/ | EPINEPHRINE | 1 | N | 0 | |||||||||||
127844871 | 12784487 | 5 | SS | BETAMETHASONE. | BETAMETHASONE | 1 | Ophthalmic | UNK | N | 0 | |||||||||
127844871 | 12784487 | 6 | SS | CYCLOPENTOLATE. | CYCLOPENTOLATE | 1 | Intraocular | 1 DF,1% STRENGTH | N | 0 | |||||||||
127844871 | 12784487 | 7 | SS | FLURBIPROFEN. | FLURBIPROFEN | 1 | Intraocular | UNK | N | 0 | |||||||||
127844871 | 12784487 | 8 | SS | HYALURONATE SODIUM | HYALURONATE SODIUM | 1 | Ophthalmic | UNK | N | 0 | |||||||||
127844871 | 12784487 | 9 | SS | LIDOCAINE. | LIDOCAINE | 1 | Unknown | 2 ML, UNK | N | 0 | 2 | ML | |||||||
127844871 | 12784487 | 10 | SS | NEOMYCIN | NEOMYCIN | 1 | Ophthalmic | UNK | N | 0 | |||||||||
127844871 | 12784487 | 11 | SS | OCUFEN | FLURBIPROFEN SODIUM | 1 | Ophthalmic | 1 DF | N | E46628, E47165, F47065 | 0 | ||||||||
127844871 | 12784487 | 12 | SS | PHENYLEPHRINE | PHENYLEPHRINEPHENYLEPHRINE HYDROCHLORIDE | 1 | Ophthalmic | 1DF, 2.5% STRENGTH | N | 0 | |||||||||
127844871 | 12784487 | 13 | SS | POVIDONE-IODINE. | POVIDONE-IODINE | 1 | UNK | N | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127844871 | 12784487 | 1 | Cataract operation |
127844871 | 12784487 | 2 | Eye irrigation |
127844871 | 12784487 | 3 | Cataract operation |
127844871 | 12784487 | 4 | Eye irrigation |
127844871 | 12784487 | 5 | Eye operation |
127844871 | 12784487 | 6 | Cataract operation |
127844871 | 12784487 | 7 | Preoperative care |
127844871 | 12784487 | 8 | Cataract operation |
127844871 | 12784487 | 10 | Eye operation |
127844871 | 12784487 | 11 | Preoperative care |
127844871 | 12784487 | 12 | Cataract operation |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127844871 | 12784487 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127844871 | 12784487 | Toxic anterior segment syndrome |
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 |
---|---|---|---|---|---|---|
127844871 | 12784487 | 1 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 3 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 5 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 6 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 7 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 8 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 9 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 10 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 11 | 20070502 | 20070502 | 0 | |
127844871 | 12784487 | 12 | 20070502 | 20070502 | 0 |