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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100173487 | 10017348 | 7 | F | 2008 | 20160805 | 20140318 | 20160813 | EXP | US-009507513-1403USA004517 | MERCK | 0.00 | F | Y | 66.21000 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100173487 | 10017348 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
| 100173487 | 10017348 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 35 MG, UNK | 20560 | 35 | MG | TABLET | |||||||
| 100173487 | 10017348 | 3 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QM | 20560 | 70 | MG | TABLET | /month | ||||||
| 100173487 | 10017348 | 4 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 1645.878 | MG | U | 0 | 70 | MG | TABLET | /wk | |||
| 100173487 | 10017348 | 5 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | UNK, UNKNOWN | 1645.878 | MG | U | 0 | TABLET | ||||||
| 100173487 | 10017348 | 6 | C | VITAMINS (UNSPECIFIED) | VITAMINS | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 100173487 | 10017348 | 1 | Osteoporosis |
| 100173487 | 10017348 | 4 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 100173487 | 10017348 | HO |
| 100173487 | 10017348 | OT |
| 100173487 | 10017348 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 100173487 | 10017348 | Arthralgia | |
| 100173487 | 10017348 | Arthritis | |
| 100173487 | 10017348 | Asthma | |
| 100173487 | 10017348 | Breast cyst | |
| 100173487 | 10017348 | Carotid endarterectomy | |
| 100173487 | 10017348 | Carpal tunnel syndrome | |
| 100173487 | 10017348 | Chronic obstructive pulmonary disease | |
| 100173487 | 10017348 | Coronary artery disease | |
| 100173487 | 10017348 | Essential hypertension | |
| 100173487 | 10017348 | Femur fracture | |
| 100173487 | 10017348 | Fibula fracture | |
| 100173487 | 10017348 | Fracture nonunion | |
| 100173487 | 10017348 | Hernia | |
| 100173487 | 10017348 | Hyperlipidaemia | |
| 100173487 | 10017348 | Inappropriate schedule of drug administration | |
| 100173487 | 10017348 | Inflammation | |
| 100173487 | 10017348 | Limb injury | |
| 100173487 | 10017348 | Osteopenia | |
| 100173487 | 10017348 | Tibia fracture | |
| 100173487 | 10017348 | Type 2 diabetes mellitus |
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 |
|---|---|---|---|---|---|---|
| 100173487 | 10017348 | 1 | 2006 | 20090711 | 0 | |
| 100173487 | 10017348 | 2 | 20110916 | 0 | ||
| 100173487 | 10017348 | 4 | 20090618 | 201102 | 0 | |
| 100173487 | 10017348 | 5 | 20110916 | 0 | ||
| 100173487 | 10017348 | 6 | 2004 | 0 |