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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4832349 | 5929992 | I | 4832349-2 | 20051104 | 20051117 | EXP | US_0511123683 | ELI LILLY AND COMPANY | 45 | YR | F | N | 20051108 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4832349 | 1006642242 | PS | CYMBALTA | 1 | 21427 | ||||||
4832349 | 1006665620 | C | LIPITOR | 1 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
4832349 | ALANINE AMINOTRANSFERASE INCREASED |
4832349 | FATIGUE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4832349 | CR |
4832349 | CSM |
Therapies reported
no results found |