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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
85784947 | 8578494 | 7 | F | 2004 | 20160721 | 20120524 | 20160725 | EXP | US-009507513-1205USA02845 | MERCK | 0.00 | F | Y | 75.00000 | KG | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
85784947 | 8578494 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
85784947 | 8578494 | 2 | SS | BONIVA | IBANDRONATE SODIUM | 1 | Oral | 150 MG, QM | U | U | 0 | 150 | MG | /month | |||||
85784947 | 8578494 | 3 | C | VITAMIN E | .ALPHA.-TOCOPHEROL | 1 | Unknown | 400 MG, UNKNOWN | U | U | 0 | 400 | MG | ||||||
85784947 | 8578494 | 4 | C | LASIX | FUROSEMIDE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
85784947 | 8578494 | 5 | C | LASIX | FUROSEMIDE | 1 | U | U | 0 | ||||||||||
85784947 | 8578494 | 6 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
85784947 | 8578494 | 7 | C | COUMADIN | WARFARIN SODIUM | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
85784947 | 8578494 | 8 | C | POTASSIUM CHLORIDE. | POTASSIUM CHLORIDE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
85784947 | 8578494 | 9 | C | CALCIUM (UNSPECIFIED) | CALCIUM | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
85784947 | 8578494 | 10 | C | ATACAND | CANDESARTAN CILEXETIL | 1 | Unknown | UNK, UNKNOWN | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
85784947 | 8578494 | 1 | Osteoporosis |
85784947 | 8578494 | 2 | Osteoporosis |
85784947 | 8578494 | 3 | Product used for unknown indication |
85784947 | 8578494 | 4 | Oedema peripheral |
85784947 | 8578494 | 5 | Hypertension |
85784947 | 8578494 | 6 | Diabetes mellitus |
85784947 | 8578494 | 7 | Deep vein thrombosis |
85784947 | 8578494 | 8 | Hypokalaemia |
85784947 | 8578494 | 9 | Product used for unknown indication |
85784947 | 8578494 | 10 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
85784947 | 8578494 | HO |
85784947 | 8578494 | DS |
85784947 | 8578494 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
85784947 | 8578494 | Acute kidney injury | |
85784947 | 8578494 | Atypical femur fracture | |
85784947 | 8578494 | Blood cholesterol increased | |
85784947 | 8578494 | Femur fracture | |
85784947 | 8578494 | Haemangioma of liver | |
85784947 | 8578494 | Hypercalcaemia | |
85784947 | 8578494 | Intramedullary rod insertion | |
85784947 | 8578494 | Low turnover osteopathy | |
85784947 | 8578494 | Osteoarthritis | |
85784947 | 8578494 | Osteoporosis | |
85784947 | 8578494 | Peripheral swelling | |
85784947 | 8578494 | Stress fracture | |
85784947 | 8578494 | Tooth disorder | |
85784947 | 8578494 | Upper respiratory tract infection |
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 |
---|---|---|---|---|---|---|
85784947 | 8578494 | 1 | 2003 | 2008 | 0 | |
85784947 | 8578494 | 2 | 20070904 | 2011 | 0 | |
85784947 | 8578494 | 3 | 1992 | 0 |