Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125213461 | 12521346 | 1 | I | 20160623 | 20160701 | 20160701 | EXP | CA-WARNER CHILCOTT, LLC-1054508 | WARNER CHILCOTT | 70.00 | YR | F | Y | 59.09000 | KG | 20160701 | OT | CA | CA |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125213461 | 12521346 | 1 | PS | ACTONEL | RISEDRONATE SODIUM | 1 | Oral | 20835 | TABLET | ||||||||||
| 125213461 | 12521346 | 2 | C | CALCIUM | CALCIUM | 1 | 0 | ||||||||||||
| 125213461 | 12521346 | 3 | C | MULTIVITAMIN | VITAMINS | 1 | 0 | ||||||||||||
| 125213461 | 12521346 | 4 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125213461 | 12521346 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125213461 | 12521346 | Atypical femur fracture | |
| 125213461 | 12521346 | Fall |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125213461 | 12521346 | 1 | 2002 | 0 |