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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5577903 | 6517137 | I | 5577903-8 | 20071218 | 20071231 | EXP | BR-ELI_LILLY_AND_COMPANY-BR200712003814 | ELI LILLY AND COMPANY | F | Y | 20071220 | CN | BRAZIL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5577903 | 1009350024 | PS | FORTEO | 1 | SUBCUTANEOUS | UNK, UNKNOWN | 021318 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5577903 | HO |
Reactions reported
Event ID | PT |
---|---|
5577903 | CARDIAC DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |