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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98134414 | 9813441 | 4 | F | 2006 | 20160801 | 20140113 | 20160805 | EXP | US-MERCK-1401USA001802 | MERCK | 0.00 | F | Y | 0.00000 | 20160805 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98134414 | 9813441 | 1 | PS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70 MG/2800, Q WEEKLY | U | 21762 | 70 | MG | TABLET | /wk | |||||
98134414 | 9813441 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | U | 0 | 70 | MG | TABLET | ||||||
98134414 | 9813441 | 3 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | U | 0 | 70 | MG | /wk | ||||||
98134414 | 9813441 | 4 | SS | ACTONEL | RISEDRONATE SODIUM | 1 | Unknown | UNK, UNKNOWN | 0 | ||||||||||
98134414 | 9813441 | 5 | SS | ACTONEL | RISEDRONATE SODIUM | 1 | 0 | ||||||||||||
98134414 | 9813441 | 6 | C | VITAMINS (UNSPECIFIED) | VITAMINS | 1 | Unknown | UNK, UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
98134414 | 9813441 | 1 | Osteoporosis |
98134414 | 9813441 | 2 | Osteoporosis |
98134414 | 9813441 | 3 | Osteoporosis |
98134414 | 9813441 | 4 | Osteoporosis |
98134414 | 9813441 | 5 | Osteopenia |
98134414 | 9813441 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
98134414 | 9813441 | OT |
98134414 | 9813441 | DS |
98134414 | 9813441 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
98134414 | 9813441 | Arthralgia | |
98134414 | 9813441 | Breast disorder female | |
98134414 | 9813441 | Cardiac disorder | |
98134414 | 9813441 | Femur fracture | |
98134414 | 9813441 | Gastrointestinal disorder | |
98134414 | 9813441 | Gastrooesophageal reflux disease | |
98134414 | 9813441 | Low turnover osteopathy | |
98134414 | 9813441 | Osteoporosis |
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 |
---|---|---|---|---|---|---|
98134414 | 9813441 | 1 | 20060424 | 200802 | 0 | |
98134414 | 9813441 | 2 | 20061005 | 0 | ||
98134414 | 9813441 | 3 | 200803 | 201302 | 0 | |
98134414 | 9813441 | 4 | 200203 | 200605 | 0 | |
98134414 | 9813441 | 6 | 1985 | 0 |