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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89046076 | 8904607 | 6 | F | 2002 | 20160726 | 20121112 | 20160729 | EXP | US-009507513-1211USA004397 | MERCK | 0.00 | F | Y | 78.46000 | KG | 20160729 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89046076 | 8904607 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | U | 20560 | 70 | MG | TABLET | /wk | |||||
| 89046076 | 8904607 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | U | 20560 | TABLET | ||||||||||
| 89046076 | 8904607 | 3 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70MG/2800 IU, UNKNOWN | 0 | TABLET | |||||||||
| 89046076 | 8904607 | 4 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | 0 | TABLET | |||||||||||
| 89046076 | 8904607 | 5 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNKNOWN | U | 0 | 70 | MG | TABLET | ||||||
| 89046076 | 8904607 | 6 | C | CALCIUM (UNSPECIFIED) | CALCIUM | 1 | 600 MG, QD | U | 0 | 600 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 89046076 | 8904607 | 1 | Osteoporosis |
| 89046076 | 8904607 | 2 | Osteopenia |
| 89046076 | 8904607 | 3 | Osteoporosis |
| 89046076 | 8904607 | 4 | Osteopenia |
| 89046076 | 8904607 | 5 | Osteoporosis |
| 89046076 | 8904607 | 6 | Routine health maintenance |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 89046076 | 8904607 | OT |
| 89046076 | 8904607 | HO |
| 89046076 | 8904607 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 89046076 | 8904607 | Anxiety | |
| 89046076 | 8904607 | Arthritis | |
| 89046076 | 8904607 | Back injury | |
| 89046076 | 8904607 | Breast conserving surgery | |
| 89046076 | 8904607 | Breast cyst excision | |
| 89046076 | 8904607 | Dental prosthesis user | |
| 89046076 | 8904607 | Depression | |
| 89046076 | 8904607 | Dermatitis contact | |
| 89046076 | 8904607 | Dyspepsia | |
| 89046076 | 8904607 | Endodontic procedure | |
| 89046076 | 8904607 | Femur fracture | |
| 89046076 | 8904607 | Fungal infection | |
| 89046076 | 8904607 | Haematocrit abnormal | |
| 89046076 | 8904607 | Hypertension | |
| 89046076 | 8904607 | Hypoaesthesia | |
| 89046076 | 8904607 | Inappropriate schedule of drug administration | |
| 89046076 | 8904607 | Infection | |
| 89046076 | 8904607 | Intramedullary rod insertion | |
| 89046076 | 8904607 | Limb injury | |
| 89046076 | 8904607 | Neck surgery | |
| 89046076 | 8904607 | Nervous system disorder | |
| 89046076 | 8904607 | Neuropathy peripheral | |
| 89046076 | 8904607 | Pain | |
| 89046076 | 8904607 | Pain in extremity | |
| 89046076 | 8904607 | Post procedural infection | |
| 89046076 | 8904607 | Sinusitis | |
| 89046076 | 8904607 | Sleep disorder | |
| 89046076 | 8904607 | Spinal operation | |
| 89046076 | 8904607 | Surgery |
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 |
|---|---|---|---|---|---|---|
| 89046076 | 8904607 | 1 | 2003 | 2010 | 0 | |
| 89046076 | 8904607 | 3 | 200605 | 200710 | 0 | |
| 89046076 | 8904607 | 6 | 1982 | 0 |