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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630657 | 6253483 | F | 5630657-9 | 20020217 | 20080206 | 20080219 | EXP | IT-ELI_LILLY_AND_COMPANY-IT200702005542 | ELI LILLY AND COMPANY | 6 | YR | M | Y | 20080219 | MD | ITALY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630657 | 1009533622 | PS | HUMATROPE | 1 | ORAL | 120 MG, DAILY (1/D) | 019640 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5630657 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5630657 | ACRODERMATITIS |
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 |
|---|---|---|---|---|---|
| 5630657 | 1009533622 | 20001001 | 20030221 | 874 | DAY |