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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98538989 | 9853898 | 9 | F | 2003 | 20160916 | 20140129 | 20160923 | EXP | US-MERCK-1401USA011320 | MERCK | 0.00 | F | Y | 55.33000 | KG | 20160923 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98538989 | 9853898 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
98538989 | 9853898 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | 20560 | TABLET | |||||||||||
98538989 | 9853898 | 3 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70 MG/5600 IU, UNK | 0 | 70 | MG | TABLET | |||||||
98538989 | 9853898 | 4 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70 MG/2800 IU, UNKNOWN | 0 | 70 | MG | TABLET | |||||||
98538989 | 9853898 | 5 | SS | ACTONEL | RISEDRONATE SODIUM | 1 | Oral | 150 MG, UNKNOWN | Y | 0 | 150 | MG | |||||||
98538989 | 9853898 | 6 | SS | ACTONEL | RISEDRONATE SODIUM | 1 | Y | 0 | |||||||||||
98538989 | 9853898 | 7 | C | CENTRUM SILVER | MINERALSVITAMINS | 1 | Oral | UNK, UNKNOWN | 0 | ||||||||||
98538989 | 9853898 | 8 | C | CALCIUM (UNSPECIFIED) | CALCIUM | 1 | Oral | 600 MG, UNKNOWN | 0 | 600 | MG | ||||||||
98538989 | 9853898 | 9 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 2000 MG, UNKNOWN | 0 | 2000 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
98538989 | 9853898 | 1 | Osteopenia |
98538989 | 9853898 | 2 | Osteoporosis |
98538989 | 9853898 | 3 | Osteopenia |
98538989 | 9853898 | 4 | Osteoporosis |
98538989 | 9853898 | 5 | Osteopenia |
98538989 | 9853898 | 6 | Osteoporosis |
98538989 | 9853898 | 7 | Routine health maintenance |
98538989 | 9853898 | 8 | Calcium deficiency |
98538989 | 9853898 | 9 | Vitamin D deficiency |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
98538989 | 9853898 | HO |
98538989 | 9853898 | OT |
98538989 | 9853898 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
98538989 | 9853898 | Arthralgia | |
98538989 | 9853898 | Femur fracture | |
98538989 | 9853898 | Fibrocystic breast disease | |
98538989 | 9853898 | Gait disturbance | |
98538989 | 9853898 | Haematocrit decreased | |
98538989 | 9853898 | Haemoglobin decreased | |
98538989 | 9853898 | Hyperlipidaemia | |
98538989 | 9853898 | Intramedullary rod insertion | |
98538989 | 9853898 | Muscular weakness | |
98538989 | 9853898 | Onychomycosis | |
98538989 | 9853898 | Ovarian cyst | |
98538989 | 9853898 | Pain | |
98538989 | 9853898 | Pain in extremity |
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 |
---|---|---|---|---|---|---|
98538989 | 9853898 | 1 | 200305 | 20060930 | 0 | |
98538989 | 9853898 | 3 | 200504 | 20101120 | 0 | |
98538989 | 9853898 | 4 | 20070724 | 0 | ||
98538989 | 9853898 | 5 | 20101120 | 20110120 | 0 | |
98538989 | 9853898 | 7 | 2000 | 0 | ||
98538989 | 9853898 | 8 | 2000 | 0 | ||
98538989 | 9853898 | 9 | 2000 | 0 |