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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8248785 | 8486005 | I | 8248785-0 | 20120317 | 20120323 | 20120331 | EXP | ES-ELI_LILLY_AND_COMPANY-ES201203007295 | ELI LILLY AND COMPANY | 86 | YR | F | Y | 60 | KG | 20120327 | CN | SPAIN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8248785 | 1019282886 | PS | FORTEO | 1 | SUBCUTANEOUS | 20 UG, QD | 021318 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8248785 | 1019282886 | OSTEOPOROSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
8248785 | DE |
Reactions reported
Event ID | PT |
---|---|
8248785 | DEATH |
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 |
---|---|---|---|---|---|
8248785 | 1019282886 | 20111125 |