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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330791 | 4106856 | F | 1 | 4330791-X | 20040212 | 20040311 | 20040331 | EXP | USA040259674 | ELI LILLY AND COMPANY | 79 | YR | F | N | 20040324 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330791 | 1004757099 | PS | FORTEO | 1 | 20 UG/1 DAY | Y | N | 21318 | |||
| 4330791 | 1004766356 | C | CALCIUM AND VITAMIN D | 2 | |||||||
| 4330791 | 1004766357 | C | ZANTAC | 1 | |||||||
| 4330791 | 1004766358 | C | RITALIN | 1 | |||||||
| 4330791 | 1004766359 | C | LOPRESSOR | 1 | |||||||
| 4330791 | 1004766360 | C | MEGACE | 1 | |||||||
| 4330791 | 1004766361 | C | TESSALON | 1 | |||||||
| 4330791 | 1004766362 | C | DITROPAN XL | 1 | |||||||
| 4330791 | 1004766363 | C | ESTRACE | 1 | |||||||
| 4330791 | 1004766364 | C | PREDNISONE | 1 | |||||||
| 4330791 | 1004766365 | C | MIRALAX | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4330791 | 1004757099 | OSTEOPOROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4330791 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4330791 | BLOOD ALBUMIN DECREASED |
| 4330791 | BLOOD CREATININE INCREASED |
| 4330791 | HYPERCALCAEMIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4330791 | HP |
Therapies reported
| no results found |