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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662498 | 7340151 | I | 6662498-8 | 20091219 | 20100330 | 20100331 | EXP | TW-MERCK-1003TWN00020 | MERCK HUMAN HEALTH DIVISION | 67 | YR | F | Y | 57 | KG | 20100401 | OT | 20100108 | TAIWAN, PROVINCE OF CHINA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662498 | 1013425026 | PS | FOSAMAX PLUS D | 1 | ORAL | 021762 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6662498 | 1013425026 | OSTEOPOROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6662498 | DE |
| 6662498 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6662498 | ASCITES |
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 |
|---|---|---|---|---|---|
| 6662498 | 1013425026 | 20091112 | 20091210 | 29 | DAY |