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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 111098105 | 11109810 | 5 | F | 2003 | 20160720 | 20150513 | 20160725 | EXP | US-009507513-1505USA004569 | MERCK | 0.00 | F | Y | 53.97000 | KG | 20160725 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 111098105 | 11109810 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | U | 20560 | 70 | MG | TABLET | ||||||
| 111098105 | 11109810 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | U | 20560 | TABLET | ||||||||||
| 111098105 | 11109810 | 3 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | U | 20560 | 70 | MG | TABLET | ||||||
| 111098105 | 11109810 | 4 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | 0 | 70 | MG | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 111098105 | 11109810 | 1 | Osteoporosis |
| 111098105 | 11109810 | 2 | Osteopenia |
| 111098105 | 11109810 | 3 | Osteoporosis |
| 111098105 | 11109810 | 4 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 111098105 | 11109810 | DS |
| 111098105 | 11109810 | HO |
| 111098105 | 11109810 | OT |
| 111098105 | 11109810 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 111098105 | 11109810 | Anal fissure | |
| 111098105 | 11109810 | Arthralgia | |
| 111098105 | 11109810 | Arthritis | |
| 111098105 | 11109810 | Atelectasis | |
| 111098105 | 11109810 | Chronic obstructive pulmonary disease | |
| 111098105 | 11109810 | Complication associated with device | |
| 111098105 | 11109810 | Death | |
| 111098105 | 11109810 | Emphysema | |
| 111098105 | 11109810 | Fall | |
| 111098105 | 11109810 | Femur fracture | |
| 111098105 | 11109810 | Foot fracture | |
| 111098105 | 11109810 | Hypercholesterolaemia | |
| 111098105 | 11109810 | Hypoxia | |
| 111098105 | 11109810 | Low turnover osteopathy | |
| 111098105 | 11109810 | Pollakiuria | |
| 111098105 | 11109810 | Pulmonary hypertension | |
| 111098105 | 11109810 | Thyroid disorder | |
| 111098105 | 11109810 | Uterine prolapse | |
| 111098105 | 11109810 | 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 |
|---|---|---|---|---|---|---|
| 111098105 | 11109810 | 1 | 2003 | 2008 | 0 | |
| 111098105 | 11109810 | 3 | 20100731 | 20120316 | 0 | |
| 111098105 | 11109810 | 4 | 20081216 | 2010 | 0 |