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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8625027 | 8646559 | F | 8625027-5 | 20080801 | 20120815 | 20120827 | EXP | US-009507513-1206USA04708 | MERCK AND CO INC | YR | Y | 20120827 | LW | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8625027 | 1020676090 | PS | FOSAMAX | 1 | ORAL | 35 MG, QW | 020560 | ||||
| 8625027 | 1020676091 | SS | FOSAMAX | 1 | ORAL | 70 MG, QW | 020560 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8625027 | 1020676090 | OSTEOPOROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8625027 | DS |
| 8625027 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8625027 | STRESS FRACTURE |
| 8625027 | KNEE ARTHROPLASTY |
| 8625027 | SURGICAL FAILURE |
| 8625027 | FEMUR FRACTURE |
| 8625027 | SURGERY |
| 8625027 | ORAL INFECTION |
| 8625027 | OSTEOPOROSIS |
| 8625027 | LOW TURNOVER OSTEOPATHY |
| 8625027 | VITAMIN D DEFICIENCY |
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 |
|---|---|---|---|---|---|
| 8625027 | 1020676090 | 20010705 | 2190 | DAY | |
| 8625027 | 1020676091 | 20051010 |