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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4330777 | 4120897 | I | 4330777-5 | 20040316 | 20040331 | EXP | USA040362014 | ELI LILLY AND COMPANY | 64 | YR | F | N | 20040324 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4330777 | 1004757072 | PS | HUMALOG | 1 | 20563 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4330777 | OT |
Reactions reported
Event ID | PT |
---|---|
4330777 | CATARACT OPERATION |
4330777 | HEPATIC CIRRHOSIS |
4330777 | PHARMACEUTICAL PRODUCT COMPLAINT |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4330777 | CSM |
Therapies reported
no results found |