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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630658 | 6556079 | I | 5630658-0 | 20071229 | 20080205 | 20080219 | EXP | TR-ELI_LILLY_AND_COMPANY-TR200802003124 | ELI LILLY AND COMPANY | M | Y | 85 | KG | 20080219 | CN | TURKEY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630658 | 1009533623 | PS | HUMALOG MIX 75/25 | 1 | SUBCUTANEOUS | 020563 | |||||
| 5630658 | 1009533624 | SS | HUMALOG MIX 75/25 | 1 | SUBCUTANEOUS | 16 IU, EACH EVENING | 020563 | ||||
| 5630658 | 1009533625 | C | BELOC ZOK | 2 | ORAL | ||||||
| 5630658 | 1009533626 | C | RAMIPRIL | 1 | ORAL | UNK, UNK | |||||
| 5630658 | 1009533627 | C | LIPITOR | 1 | ORAL | UNK, UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5630658 | 1009533625 | CARDIOVASCULAR DISORDER |
| 5630658 | 1009533626 | HYPERTENSION |
| 5630658 | 1009533627 | CARDIOVASCULAR DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5630658 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5630658 | BLOOD GLUCOSE INCREASED |
| 5630658 | BRAIN NEOPLASM |
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 |
|---|---|---|---|---|---|
| 5630658 | 1009533623 | 20071101 | |||
| 5630658 | 1009533624 | 20071101 | |||
| 5630658 | 1009533625 | 20040101 | |||
| 5630658 | 1009533626 | 20040101 | |||
| 5630658 | 1009533627 | 20040101 |