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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8555629 | 8695829 | I | 8555629-6 | 20120124 | 20120717 | 20120731 | EXP | US-ELI_LILLY_AND_COMPANY-US201207005587 | ELI LILLY AND COMPANY | 39 | YR | F | Y | 20120726 | CN | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8555629 | 1020411190 | PS | ZYPREXA RELPREVV | 1 | UNK | 022173 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
8555629 | HO |
Reactions reported
Event ID | PT |
---|---|
8555629 | HOSPITALISATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
8555629 | 1020411190 | 20120113 |