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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124370672 | 12437067 | 2 | F | 2001 | 20160728 | 20160606 | 20160805 | EXP | US-009507513-1606USA001685 | MERCK | 0.00 | F | Y | 0.00000 | 20160805 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124370672 | 12437067 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | U | 20560 | 70 | MG | TABLET | ||||||
| 124370672 | 12437067 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | U | 20560 | TABLET | ||||||||||
| 124370672 | 12437067 | 3 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70 MG, UNK | U | 0 | 70 | MG | TABLET | ||||||
| 124370672 | 12437067 | 4 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | U | 20560 | 70 | MG | TABLET | /wk | |||||
| 124370672 | 12437067 | 5 | SS | FORTEO | TERIPARATIDE | 1 | Subcutaneous | 20 MCG SQ Q 24 HRS. | U | 0 | |||||||||
| 124370672 | 12437067 | 6 | SS | RECLAST | ZOLEDRONIC ACID | 1 | Intravenous bolus | 2.5 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124370672 | 12437067 | 1 | Osteoporosis |
| 124370672 | 12437067 | 2 | Osteopenia |
| 124370672 | 12437067 | 3 | Osteoporosis |
| 124370672 | 12437067 | 4 | Osteoporosis |
| 124370672 | 12437067 | 5 | Osteoporosis |
| 124370672 | 12437067 | 6 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124370672 | 12437067 | DS |
| 124370672 | 12437067 | OT |
| 124370672 | 12437067 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124370672 | 12437067 | Abdominal distension | |
| 124370672 | 12437067 | Blood cholesterol increased | |
| 124370672 | 12437067 | Bone density decreased | |
| 124370672 | 12437067 | Fall | |
| 124370672 | 12437067 | Femur fracture | |
| 124370672 | 12437067 | Intervertebral disc protrusion | |
| 124370672 | 12437067 | Nerve root compression | |
| 124370672 | 12437067 | Osteoporosis | |
| 124370672 | 12437067 | Patella fracture | |
| 124370672 | 12437067 | Rib fracture | |
| 124370672 | 12437067 | Stress fracture | |
| 124370672 | 12437067 | Tooth disorder |
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 |
|---|---|---|---|---|---|---|
| 124370672 | 12437067 | 1 | 1997 | 2007 | 0 | |
| 124370672 | 12437067 | 3 | 20071024 | 20111221 | 0 | |
| 124370672 | 12437067 | 4 | 20101221 | 201101 | 0 | |
| 124370672 | 12437067 | 5 | 2011 | 0 | ||
| 124370672 | 12437067 | 6 | 20111010 | 20120327 | 0 |