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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577896 | 6517131 | I | 5577896-3 | 20070101 | 20071218 | 20071231 | EXP | ES-ELI_LILLY_AND_COMPANY-ES200712003812 | ELI LILLY AND COMPANY | 69 | YR | F | Y | 20071224 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577896 | 1009349993 | PS | FORTEO | 1 | SUBCUTANEOUS | 20 UG, UNKNOWN | 021318 | ||||
| 5577896 | 1009349994 | C | CORTICOSTEROIDS | 2 | UNK, UNKNOWN | ||||||
| 5577896 | 1009349995 | C | ANTIHYPERTENSIVES | 2 | UNK, UNKNOWN | ||||||
| 5577896 | 1009349996 | C | MORPHINE | 1 | UNK, UNKNOWN | ||||||
| 5577896 | 1009349997 | C | LYRICA | 1 | UNK, UNKNOWN | ||||||
| 5577896 | 1009349998 | C | ANTIDEPRESSANTS | 2 | UNK, UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577896 | 1009349993 | OSTEOPOROSIS |
| 5577896 | 1009349995 | HYPERTENSION |
| 5577896 | 1009349996 | PAIN |
| 5577896 | 1009349998 | DEPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577896 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5577896 | PAIN |
| 5577896 | RESPIRATORY FAILURE |
| 5577896 | WEIGHT DECREASED |
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 |
|---|---|---|---|---|---|
| 5577896 | 1009349993 | 20060401 | 20071001 |