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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105708335 | 10570833 | 5 | F | 2004 | 20160824 | 20141107 | 20160830 | EXP | US-009507513-1411USA000588 | MERCK | 0.00 | F | Y | 0.00000 | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105708335 | 10570833 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 10 MG, QD | 20560 | 10 | MG | TABLET | QD | ||||||
| 105708335 | 10570833 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | UNK | 20560 | TABLET | |||||||||
| 105708335 | 10570833 | 3 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70MG/2800 IU | 0 | TABLET | |||||||||
| 105708335 | 10570833 | 4 | SS | BONIVA | IBANDRONATE SODIUM | 1 | Oral | UNK, QM | U | U | 0 | /month | |||||||
| 105708335 | 10570833 | 5 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | 0 | 70 | MG | TABLET | |||||||
| 105708335 | 10570833 | 6 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | 0 | 70 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 105708335 | 10570833 | 1 | Osteoporosis |
| 105708335 | 10570833 | 3 | Osteoporosis |
| 105708335 | 10570833 | 4 | Osteoporosis |
| 105708335 | 10570833 | 5 | Product used for unknown indication |
| 105708335 | 10570833 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 105708335 | 10570833 | DS |
| 105708335 | 10570833 | HO |
| 105708335 | 10570833 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 105708335 | 10570833 | Alopecia | |
| 105708335 | 10570833 | Arthropathy | |
| 105708335 | 10570833 | Back injury | |
| 105708335 | 10570833 | Back pain | |
| 105708335 | 10570833 | Blood chromium increased | |
| 105708335 | 10570833 | Drug hypersensitivity | |
| 105708335 | 10570833 | Emotional distress | |
| 105708335 | 10570833 | Fatigue | |
| 105708335 | 10570833 | Femur fracture | |
| 105708335 | 10570833 | Gastric bypass | |
| 105708335 | 10570833 | Goitre | |
| 105708335 | 10570833 | Hip arthroplasty | |
| 105708335 | 10570833 | Hypothyroidism | |
| 105708335 | 10570833 | Hysterectomy | |
| 105708335 | 10570833 | Joint arthroplasty | |
| 105708335 | 10570833 | Joint injury | |
| 105708335 | 10570833 | Malnutrition | |
| 105708335 | 10570833 | Muscle spasms | |
| 105708335 | 10570833 | Nephrolithiasis | |
| 105708335 | 10570833 | Osteoarthritis | |
| 105708335 | 10570833 | Osteopenia | |
| 105708335 | 10570833 | Pain | |
| 105708335 | 10570833 | Pelvic fracture | |
| 105708335 | 10570833 | Road traffic accident | |
| 105708335 | 10570833 | Upper limb fracture | |
| 105708335 | 10570833 | Vitamin D deficiency | |
| 105708335 | 10570833 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 105708335 | 10570833 | 1 | 2004 | 2007 | 0 | |
| 105708335 | 10570833 | 2 | 200512 | 201104 | 0 | |
| 105708335 | 10570833 | 3 | 200702 | 200802 | 0 | |
| 105708335 | 10570833 | 4 | 2000 | 0 | ||
| 105708335 | 10570833 | 5 | 200803 | 2008 | 0 | |
| 105708335 | 10570833 | 6 | 200809 | 20110309 | 0 |