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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89637784 | 8963778 | 4 | F | 2005 | 20160729 | 20121213 | 20160807 | EXP | US-009507513-1212USA004742 | MERCK | 0.00 | F | Y | 0.00000 | 20160807 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89637784 | 8963778 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
| 89637784 | 8963778 | 2 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70MG-2,800 | 0 | 70 | MG | TABLET | |||||||
| 89637784 | 8963778 | 3 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | 20560 | 70 | MG | TABLET | |||||||
| 89637784 | 8963778 | 4 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | U | 0 | 70 | MG | |||||||
| 89637784 | 8963778 | 5 | C | DIDRONEL | ETIDRONATE DISODIUM | 1 | Oral | UNK | U | 0 | |||||||||
| 89637784 | 8963778 | 6 | C | PREDNISONE. | PREDNISONE | 1 | INTERMITTENTLY | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 89637784 | 8963778 | 1 | Osteoporosis |
| 89637784 | 8963778 | 2 | Osteoporosis |
| 89637784 | 8963778 | 3 | Osteoporosis |
| 89637784 | 8963778 | 4 | Osteoporosis |
| 89637784 | 8963778 | 5 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 89637784 | 8963778 | HO |
| 89637784 | 8963778 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 89637784 | 8963778 | Appendicectomy | |
| 89637784 | 8963778 | Arterial haemorrhage | |
| 89637784 | 8963778 | Atrial fibrillation | |
| 89637784 | 8963778 | Biopsy bone | |
| 89637784 | 8963778 | Body height decreased | |
| 89637784 | 8963778 | Bronchitis | |
| 89637784 | 8963778 | Deep vein thrombosis | |
| 89637784 | 8963778 | Depression | |
| 89637784 | 8963778 | Dyslipidaemia | |
| 89637784 | 8963778 | Echocardiogram abnormal | |
| 89637784 | 8963778 | Femur fracture | |
| 89637784 | 8963778 | Hypertension | |
| 89637784 | 8963778 | Hysterectomy | |
| 89637784 | 8963778 | Intramedullary rod insertion | |
| 89637784 | 8963778 | Knee arthroplasty | |
| 89637784 | 8963778 | Kyphosis | |
| 89637784 | 8963778 | Pain in extremity | |
| 89637784 | 8963778 | Parkinson's disease | |
| 89637784 | 8963778 | Pulmonary mass | |
| 89637784 | 8963778 | Retroperitoneal haematoma | |
| 89637784 | 8963778 | Spinal compression fracture | |
| 89637784 | 8963778 | Synovial cyst | |
| 89637784 | 8963778 | Therapeutic embolisation | |
| 89637784 | 8963778 | Vertebroplasty |
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 |
|---|---|---|---|---|---|---|
| 89637784 | 8963778 | 1 | 200207 | 200612 | 0 | |
| 89637784 | 8963778 | 2 | 200701 | 201003 | 0 | |
| 89637784 | 8963778 | 3 | 20050502 | 20061109 | 0 | |
| 89637784 | 8963778 | 4 | 20091214 | 0 | ||
| 89637784 | 8963778 | 5 | 2001 | 2002 | 0 | |
| 89637784 | 8963778 | 6 | 2000 | 2011 | 0 |