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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89779743 | 8977974 | 3 | F | 2000 | 20160728 | 20121219 | 20160804 | EXP | US-009507513-1212USA006809 | MERCK | 0.00 | F | Y | 0.00000 | 20160804 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89779743 | 8977974 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | UNK | U | 20560 | TABLET | ||||||||
| 89779743 | 8977974 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 10 MG, QD | U | 20560 | 10 | MG | TABLET | QD | |||||
| 89779743 | 8977974 | 3 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | UNK | U | 20560 | TABLET | ||||||||
| 89779743 | 8977974 | 4 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | U | 0 | 70 | MG | /wk | ||||||
| 89779743 | 8977974 | 5 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | U | 0 | |||||||||||
| 89779743 | 8977974 | 6 | C | VITAMINS (UNSPECIFIED) | VITAMINS | 1 | Unknown | U | 0 | ||||||||||
| 89779743 | 8977974 | 7 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | UNK | U | 20560 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 89779743 | 8977974 | 1 | Prophylaxis |
| 89779743 | 8977974 | 2 | Bone density decreased |
| 89779743 | 8977974 | 4 | Prophylaxis |
| 89779743 | 8977974 | 5 | Bone density decreased |
| 89779743 | 8977974 | 6 | Product used for unknown indication |
| 89779743 | 8977974 | 7 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 89779743 | 8977974 | OT |
| 89779743 | 8977974 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 89779743 | 8977974 | Acute kidney injury | |
| 89779743 | 8977974 | Arthritis | |
| 89779743 | 8977974 | Balance disorder | |
| 89779743 | 8977974 | Blood cholesterol increased | |
| 89779743 | 8977974 | Chronic kidney disease | |
| 89779743 | 8977974 | Constipation | |
| 89779743 | 8977974 | Coronary artery disease | |
| 89779743 | 8977974 | Femur fracture | |
| 89779743 | 8977974 | Fungal infection | |
| 89779743 | 8977974 | Gastrooesophageal reflux disease | |
| 89779743 | 8977974 | Gout | |
| 89779743 | 8977974 | Haemorrhagic anaemia | |
| 89779743 | 8977974 | Hyperlipidaemia | |
| 89779743 | 8977974 | Lactose intolerance | |
| 89779743 | 8977974 | Osteoarthritis | |
| 89779743 | 8977974 | Peripheral arterial occlusive disease | |
| 89779743 | 8977974 | Periprosthetic fracture | |
| 89779743 | 8977974 | Postoperative ileus | |
| 89779743 | 8977974 | Shoulder arthroplasty | |
| 89779743 | 8977974 | Skin cancer | |
| 89779743 | 8977974 | Tooth fracture |
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 |
|---|---|---|---|---|---|---|
| 89779743 | 8977974 | 1 | 1995 | 200804 | 0 | |
| 89779743 | 8977974 | 2 | 20060815 | 200804 | 0 | |
| 89779743 | 8977974 | 3 | 2010 | 0 | ||
| 89779743 | 8977974 | 4 | 20080508 | 2010 | 0 | |
| 89779743 | 8977974 | 7 | 1995 | 200804 | 0 |