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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577897 | 6517132 | I | 5577897-5 | 20071201 | 20071217 | 20071231 | EXP | ES-ELI_LILLY_AND_COMPANY-ES200712003803 | ELI LILLY AND COMPANY | 77 | YR | F | Y | 20071221 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577897 | 1009349999 | PS | FORTEO | 1 | SUBCUTANEOUS | 20 UG, UNKNOWN | 021318 | ||||
| 5577897 | 1009350000 | C | ANALGESICS | 2 | UNKNOWN | UNK, UNKNOWN | |||||
| 5577897 | 1009350001 | C | OMEPRAZOLE | 2 | UNKNOWN | UNK, UNKNOWN | |||||
| 5577897 | 1009350002 | C | ORFIDAL | 2 | UNKNOWN | UNK, UNKNOWN | |||||
| 5577897 | 1009350003 | C | CALCIUM | 2 | UNKNOWN | UNK, UNKNOWN | |||||
| 5577897 | 1009350004 | C | SOMAZINA | 2 | UNKNOWN | UNK, UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577897 | 1009349999 | OSTEOPOROSIS |
| 5577897 | 1009350000 | PAIN |
| 5577897 | 1009350001 | GASTRIC DISORDER |
| 5577897 | 1009350002 | NERVOUSNESS |
| 5577897 | 1009350003 | OSTEOPOROSIS |
| 5577897 | 1009350004 | MEMORY IMPAIRMENT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577897 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5577897 | AMNESIA |
| 5577897 | EPILEPSY |
| 5577897 | FOAMING AT MOUTH |
| 5577897 | LOSS OF CONSCIOUSNESS |
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 |
|---|---|---|---|---|---|
| 5577897 | 1009349999 | 20070626 |