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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903982 | 6775698 | F | 5903982-1 | 20000101 | 20080926 | 20080930 | EXP | US-MERCK-0805USA00896 | MERCK HUMAN HEALTH DIVISION | 56 | YR | F | Y | 20081001 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903982 | 1010522445 | PS | FOSAMAX | 1 | ORAL | 20560 | |||||
| 5903982 | 1010522446 | SS | FOSAMAX | 1 | ORAL | 020560 | |||||
| 5903982 | 1010522447 | SS | ACTONEL | 1 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5903982 | 1010522445 | OSTEOPENIA |
| 5903982 | 1010522447 | OSTEOPENIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5903982 | HO |
| 5903982 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5903982 | JAW DISORDER |
| 5903982 | KIDNEY INFECTION |
| 5903982 | MOUTH ULCERATION |
| 5903982 | OSTEONECROSIS |
| 5903982 | OVARIAN CYST |
| 5903982 | OVERDOSE |
| 5903982 | PAIN IN JAW |
| 5903982 | UTERINE LEIOMYOMA |
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 |
|---|---|---|---|---|---|
| 5903982 | 1010522445 | 19970101 | 19980101 | 1 | YR |
| 5903982 | 1010522446 | 20020101 | 20040101 | 2 | YR |
| 5903982 | 1010522447 | 20040101 | 20061102 | 2 | YR |