Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4332167 | 4122505 | I | 4332167-8 | 20040316 | 20040331 | EXP | CA_040306759 | ELI LILLY AND COMPANY | 65 | YR | F | N | 20040324 | OT |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4332167 | 1004762060 | PS | ZYPREXA | 1 | ORAL | 5 MG | 20592 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4332167 | OT |
Reactions reported
Event ID | PT |
---|---|
4332167 | TRANSIENT ISCHAEMIC ATTACK |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4332167 | CR |
4332167 | FGN |
4332167 | HP |
4332167 | OTH |
Therapies reported
no results found |