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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4428107 | 4206389 | I | 4428107-3 | 20030807 | 20040331 | 20040726 | PER | USA030843650 | ELI LILLY AND COMPANY | 67 | YR | F | N | 43 | KG | 20040607 | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4428107 | 1005119661 | PS | FORTEO | 1 | 20 UG DAY | D | FF3B21C | 20050101 | 21318 | ||
| 4428107 | 1005129042 | C | CALCIUM | 2 | |||||||
| 4428107 | 1005129043 | C | MULTI-VITAMIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4428107 | 1005119661 | OSTEOPOROSIS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 4428107 | INJECTION SITE HAEMORRHAGE |
| 4428107 | OEDEMA PERIPHERAL |
| 4428107 | PAIN IN EXTREMITY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4428107 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4428107 | 1005119661 | 20030806 |