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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1087956110 | 10879561 | 10 | F | 2005 | 20160728 | 20150302 | 20160802 | EXP | US-MERCK-1503USA000432 | MERCK | 0.00 | F | Y | 71.66000 | KG | 20160802 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1087956110 | 10879561 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 10 MG, UNK | Y | 20560 | 10 | MG | TABLET | ||||||
1087956110 | 10879561 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | Y | 20560 | 70 | MG | TABLET | ||||||
1087956110 | 10879561 | 3 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | Y | 20560 | 70 | MG | TABLET | /wk | |||||
1087956110 | 10879561 | 4 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 35 MG, QW | Y | 20560 | 35 | MG | TABLET | /wk | |||||
1087956110 | 10879561 | 5 | SS | BONIVA | IBANDRONATE SODIUM | 1 | Oral | 150 MG, UNK | 0 | 150 | MG | ||||||||
1087956110 | 10879561 | 6 | SS | BONIVA | IBANDRONATE SODIUM | 1 | 0 | ||||||||||||
1087956110 | 10879561 | 7 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | Y | 20560 | 70 | MG | TABLET | ||||||
1087956110 | 10879561 | 8 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Y | 20560 | TABLET | ||||||||||
1087956110 | 10879561 | 9 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Unknown | 70 MG, UNK | 0 | 70 | MG | ||||||||
1087956110 | 10879561 | 10 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | 0 | ||||||||||||
1087956110 | 10879561 | 11 | C | ASCORBIC ACID. | ASCORBIC ACID | 1 | Oral | 3 PILLS A DAY OF VITAMIN C W CAL-CITRATE | U | U | 0 | 200 | MG | TID | |||||
1087956110 | 10879561 | 12 | C | CAL-CITRATE | 2 | Oral | 3 PILLS A DAY OF VITAMIN C W CAL-CITRATE | U | U | 0 | 200 | MG | TID | ||||||
1087956110 | 10879561 | 13 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 2 PILLS A DAY | U | U | 0 | 200 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
1087956110 | 10879561 | 1 | Osteopenia |
1087956110 | 10879561 | 2 | Osteoporosis postmenopausal |
1087956110 | 10879561 | 5 | Osteopenia |
1087956110 | 10879561 | 6 | Osteoporosis postmenopausal |
1087956110 | 10879561 | 7 | Osteopenia |
1087956110 | 10879561 | 8 | Osteoporosis postmenopausal |
1087956110 | 10879561 | 9 | Osteopenia |
1087956110 | 10879561 | 10 | Osteoporosis postmenopausal |
1087956110 | 10879561 | 11 | Product used for unknown indication |
1087956110 | 10879561 | 12 | Product used for unknown indication |
1087956110 | 10879561 | 13 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
1087956110 | 10879561 | OT |
1087956110 | 10879561 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
1087956110 | 10879561 | Anxiety | |
1087956110 | 10879561 | Arthralgia | |
1087956110 | 10879561 | Back pain | |
1087956110 | 10879561 | Bone loss | |
1087956110 | 10879561 | Calcium deficiency | |
1087956110 | 10879561 | Chills | |
1087956110 | 10879561 | Depression | |
1087956110 | 10879561 | Femur fracture | |
1087956110 | 10879561 | Foot fracture | |
1087956110 | 10879561 | Gait disturbance | |
1087956110 | 10879561 | Gingival bleeding | |
1087956110 | 10879561 | Neck pain | |
1087956110 | 10879561 | Pain in extremity | |
1087956110 | 10879561 | Periodontal operation | |
1087956110 | 10879561 | Pollakiuria | |
1087956110 | 10879561 | Sleep disorder | |
1087956110 | 10879561 | Treatment noncompliance | |
1087956110 | 10879561 | Vitamin D deficiency |
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 |
---|---|---|---|---|---|---|
1087956110 | 10879561 | 1 | 20000712 | 20001129 | 0 | |
1087956110 | 10879561 | 2 | 20001221 | 20060406 | 0 | |
1087956110 | 10879561 | 3 | 20120717 | 201302 | 0 | |
1087956110 | 10879561 | 4 | 20130225 | 201305 | 0 | |
1087956110 | 10879561 | 5 | 20060422 | 20090308 | 0 | |
1087956110 | 10879561 | 7 | 20120906 | 201305 | 0 | |
1087956110 | 10879561 | 9 | 20120906 | 20130618 | 0 | |
1087956110 | 10879561 | 11 | 2000 | 0 | ||
1087956110 | 10879561 | 12 | 2000 | 0 | ||
1087956110 | 10879561 | 13 | 2000 | 0 |