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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88689956 | 8868995 | 6 | F | 2009 | 20160808 | 20121027 | 20160813 | EXP | US-009507513-1210USA006577 | MERCK | 0.00 | F | Y | 0.00000 | 20160813 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88689956 | 8868995 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | U | 20560 | 70 | MG | TABLET | ||||||
| 88689956 | 8868995 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | U | 20560 | TABLET | ||||||||||
| 88689956 | 8868995 | 3 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | U | 20560 | 70 | MG | TABLET | ||||||
| 88689956 | 8868995 | 4 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | U | 20560 | TABLET | ||||||||||
| 88689956 | 8868995 | 5 | C | OSCAL | CALCIUM CARBONATE | 1 | Oral | 500 MG, QD | U | 0 | 500 | MG | QD | ||||||
| 88689956 | 8868995 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88689956 | 8868995 | 1 | Osteoporosis |
| 88689956 | 8868995 | 2 | Osteopenia |
| 88689956 | 8868995 | 3 | Osteoporosis |
| 88689956 | 8868995 | 4 | Osteopenia |
| 88689956 | 8868995 | 5 | Routine health maintenance |
| 88689956 | 8868995 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 88689956 | 8868995 | OT |
| 88689956 | 8868995 | HO |
| 88689956 | 8868995 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88689956 | 8868995 | Bone disorder | |
| 88689956 | 8868995 | Diabetes mellitus | |
| 88689956 | 8868995 | Fall | |
| 88689956 | 8868995 | Femur fracture | |
| 88689956 | 8868995 | Hip fracture | |
| 88689956 | 8868995 | Hypercholesterolaemia | |
| 88689956 | 8868995 | Hypertension | |
| 88689956 | 8868995 | Impaired healing | |
| 88689956 | 8868995 | Low turnover osteopathy | |
| 88689956 | 8868995 | Musculoskeletal disorder | |
| 88689956 | 8868995 | Stress fracture | |
| 88689956 | 8868995 | Thrombosis |
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 |
|---|---|---|---|---|---|---|
| 88689956 | 8868995 | 1 | 2001 | 200802 | 0 | |
| 88689956 | 8868995 | 3 | 20080303 | 201003 | 0 | |
| 88689956 | 8868995 | 5 | 2003 | 0 | ||
| 88689956 | 8868995 | 6 | 200808 | 0 |