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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98501126 | 9850112 | 6 | F | 2009 | 20160908 | 20140128 | 20160914 | EXP | US-009507513-1401USA008386 | MERCK | 0.00 | F | Y | 0.00000 | 20160914 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98501126 | 9850112 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 10 MG, QD | 20560 | 10 | MG | TABLET | QD | ||||||
| 98501126 | 9850112 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
| 98501126 | 9850112 | 3 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 0 | 70 | MG | /wk | |||||||
| 98501126 | 9850112 | 4 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | 50000 IU, QW | 0 | 50000 | IU | /wk | |||||||
| 98501126 | 9850112 | 5 | C | VITAMIN B (UNSPECIFIED) | 2 | Unknown | 100 IU, QD | 0 | 100 | IU | QD | ||||||||
| 98501126 | 9850112 | 6 | C | ASCORBIC ACID. | ASCORBIC ACID | 1 | Unknown | 500 IU, QD | 0 | 500 | IU | QD | |||||||
| 98501126 | 9850112 | 7 | C | CALCIUM (UNSPECIFIED) | CALCIUM | 1 | Unknown | 600 MG, QD | 0 | 600 | MG | QD | |||||||
| 98501126 | 9850112 | 8 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 98501126 | 9850112 | 9 | C | SELECTIVE ESTROGEN RECEPTOR MODULATOR (UNSPECIFIED) | 2 | Unknown | UNK, UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 98501126 | 9850112 | 1 | Osteoporosis |
| 98501126 | 9850112 | 3 | Osteoporosis |
| 98501126 | 9850112 | 4 | Product used for unknown indication |
| 98501126 | 9850112 | 5 | Product used for unknown indication |
| 98501126 | 9850112 | 6 | Product used for unknown indication |
| 98501126 | 9850112 | 7 | Product used for unknown indication |
| 98501126 | 9850112 | 8 | Product used for unknown indication |
| 98501126 | 9850112 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 98501126 | 9850112 | DE |
| 98501126 | 9850112 | HO |
| 98501126 | 9850112 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 98501126 | 9850112 | Adverse event | |
| 98501126 | 9850112 | Arteriosclerosis | |
| 98501126 | 9850112 | Death | |
| 98501126 | 9850112 | Femur fracture | |
| 98501126 | 9850112 | Intramedullary rod insertion | |
| 98501126 | 9850112 | Osteoarthritis | |
| 98501126 | 9850112 | Spinal fracture | |
| 98501126 | 9850112 | 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 |
|---|---|---|---|---|---|---|
| 98501126 | 9850112 | 1 | 19981102 | 200107 | 0 | |
| 98501126 | 9850112 | 2 | 20010720 | 200807 | 0 | |
| 98501126 | 9850112 | 3 | 200807 | 201101 | 0 | |
| 98501126 | 9850112 | 4 | 2002 | 2011 | 0 | |
| 98501126 | 9850112 | 5 | 2002 | 2011 | 0 | |
| 98501126 | 9850112 | 6 | 2002 | 2011 | 0 | |
| 98501126 | 9850112 | 7 | 2002 | 2011 | 0 | |
| 98501126 | 9850112 | 8 | 2000 | 2012 | 0 | |
| 98501126 | 9850112 | 9 | 20000623 | 2011 | 0 |