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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 101838837 | 10183883 | 7 | F | 20050202 | 20160728 | 20140520 | 20160802 | EXP | US-009507513-1405USA006479 | MERCK | 0.00 | F | Y | 46.26000 | KG | 20160802 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 101838837 | 10183883 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 10 MG, QD | 20560 | 10 | MG | TABLET | QD | ||||||
| 101838837 | 10183883 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
| 101838837 | 10183883 | 3 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
| 101838837 | 10183883 | 4 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70 MG,/2800IU QW | 0 | 70 | MG | TABLET | /wk | ||||||
| 101838837 | 10183883 | 5 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70 MG QW | 0 | 70 | MG | TABLET | /wk | ||||||
| 101838837 | 10183883 | 6 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Unknown | UNK, UNKNOWN | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 101838837 | 10183883 | 1 | Osteoporosis |
| 101838837 | 10183883 | 4 | Osteoporosis |
| 101838837 | 10183883 | 6 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 101838837 | 10183883 | DS |
| 101838837 | 10183883 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 101838837 | 10183883 | Back pain | |
| 101838837 | 10183883 | Blood disorder | |
| 101838837 | 10183883 | Calcium deficiency | |
| 101838837 | 10183883 | Dry eye | |
| 101838837 | 10183883 | Dry mouth | |
| 101838837 | 10183883 | Femoral neck fracture | |
| 101838837 | 10183883 | Femur fracture | |
| 101838837 | 10183883 | Fracture nonunion | |
| 101838837 | 10183883 | Fractured sacrum | |
| 101838837 | 10183883 | Gastric ulcer | |
| 101838837 | 10183883 | Headache | |
| 101838837 | 10183883 | Hip fracture | |
| 101838837 | 10183883 | Hormone therapy | |
| 101838837 | 10183883 | Intramedullary rod insertion | |
| 101838837 | 10183883 | Joint contracture | |
| 101838837 | 10183883 | Joint effusion | |
| 101838837 | 10183883 | Low turnover osteopathy | |
| 101838837 | 10183883 | Lower limb fracture | |
| 101838837 | 10183883 | Medical device removal | |
| 101838837 | 10183883 | Neuropathy peripheral | |
| 101838837 | 10183883 | Radiculopathy | |
| 101838837 | 10183883 | Sinusitis | |
| 101838837 | 10183883 | Spinal compression fracture | |
| 101838837 | 10183883 | Stress fracture | |
| 101838837 | 10183883 | Vision blurred | |
| 101838837 | 10183883 | Vitamin D deficiency |
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 |
|---|---|---|---|---|---|---|
| 101838837 | 10183883 | 1 | 20030823 | 0 | ||
| 101838837 | 10183883 | 2 | 20040621 | 20100527 | 0 | |
| 101838837 | 10183883 | 3 | 200308 | 200704 | 0 | |
| 101838837 | 10183883 | 4 | 20071001 | 20081021 | 0 | |
| 101838837 | 10183883 | 5 | 200704 | 200901 | 0 | |
| 101838837 | 10183883 | 6 | 200802 | 20090504 | 0 |