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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577898 | 6517133 | I | 5577898-7 | 20071214 | 20071218 | 20071231 | EXP | ES-ELI_LILLY_AND_COMPANY-ES200712003788 | ELI LILLY AND COMPANY | 70 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577898 | 1009350005 | PS | FORTEO | 1 | SUBCUTANEOUS | 20 UG, UNKNOWN | 021318 | ||||
| 5577898 | 1009350006 | C | NOLOTIL | 2 | ORAL | UNK, UNKNOWN | |||||
| 5577898 | 1009350007 | C | TRAUMEEL S | 2 | ORAL | UNK, 3/D | |||||
| 5577898 | 1009350008 | C | NEURAPAS | 2 | ORAL | UNK, 4/D | |||||
| 5577898 | 1009350009 | C | VITAMINS | 2 | ORAL | ||||||
| 5577898 | 1009350010 | C | ORFIDAL | 2 | ORAL | UNK, UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577898 | 1009350005 | OSTEOPOROSIS |
| 5577898 | 1009350006 | PAIN |
| 5577898 | 1009350008 | ANXIETY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577898 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5577898 | BACK PAIN |
| 5577898 | FALL |
| 5577898 | SPINAL FRACTURE |
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 |
|---|---|---|---|---|---|
| 5577898 | 1009350005 | 20070704 |