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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5001494 | 6044772 | F | 5001494-3 | 20060503 | 20060512 | EXP | DE-MERCK-0605DEU00065 | MERCK HUMAN HEALTH DIVISION | 78 | YR | F | Y | 60 | KG | 20060515 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5001494 | 1007281963 | PS | FOSAMAX | 1 | ORAL | 020560 | |||||
| 5001494 | 1007281964 | C | BISOPROLOL | 2 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5001494 | 1007281963 | OSTEOPOROSIS |
| 5001494 | 1007281964 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5001494 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5001494 | VAGINAL HAEMORRHAGE |
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 |
|---|---|---|---|---|---|
| 5001494 | 1007281963 | 20041105 | 20060411 | 523 | DAY |
| 5001494 | 1007281964 | 20041105 |