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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88609627 | 8860962 | 7 | F | 2006 | 20160720 | 20121025 | 20160722 | EXP | US-009507513-1210USA005986 | MERCK | 0.00 | F | Y | 0.00000 | 20160722 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88609627 | 8860962 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 35 MG, UNK | 20560 | 35 | MG | TABLET | |||||||
| 88609627 | 8860962 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, UNK | 20560 | 70 | MG | TABLET | |||||||
| 88609627 | 8860962 | 3 | SS | BONIVA | IBANDRONATE SODIUM | 1 | Unknown | 150 MG, UNK | 0 | 150 | MG | TABLET | |||||||
| 88609627 | 8860962 | 4 | C | NAPROXEN. | NAPROXEN | 1 | Unknown | 500 MG, UNK | U | 0 | 500 | MG | |||||||
| 88609627 | 8860962 | 5 | C | NAPROXEN. | NAPROXEN | 1 | U | 0 | |||||||||||
| 88609627 | 8860962 | 6 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | 500 MG, UNK | U | 0 | 500 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88609627 | 8860962 | 1 | Osteoporosis |
| 88609627 | 8860962 | 2 | Osteopenia |
| 88609627 | 8860962 | 3 | Osteoporosis |
| 88609627 | 8860962 | 4 | Inflammation |
| 88609627 | 8860962 | 5 | Pain |
| 88609627 | 8860962 | 6 | Diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 88609627 | 8860962 | DS |
| 88609627 | 8860962 | OT |
| 88609627 | 8860962 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88609627 | 8860962 | Adverse drug reaction | |
| 88609627 | 8860962 | Arthritis | |
| 88609627 | 8860962 | Diarrhoea | |
| 88609627 | 8860962 | Drug intolerance | |
| 88609627 | 8860962 | Fall | |
| 88609627 | 8860962 | Femur fracture | |
| 88609627 | 8860962 | Haemoglobin decreased | |
| 88609627 | 8860962 | Hip arthroplasty | |
| 88609627 | 8860962 | Hypertension | |
| 88609627 | 8860962 | Hysterectomy | |
| 88609627 | 8860962 | Low turnover osteopathy | |
| 88609627 | 8860962 | Myalgia | |
| 88609627 | 8860962 | Open reduction of fracture | |
| 88609627 | 8860962 | Osteoarthritis | |
| 88609627 | 8860962 | Osteopenia | |
| 88609627 | 8860962 | Renal failure | |
| 88609627 | 8860962 | Rib fracture | |
| 88609627 | 8860962 | Transfusion | |
| 88609627 | 8860962 | Tremor | |
| 88609627 | 8860962 | Urinary 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 |
|---|---|---|---|---|---|---|
| 88609627 | 8860962 | 1 | 200609 | 200707 | 0 | |
| 88609627 | 8860962 | 2 | 200306 | 200512 | 0 | |
| 88609627 | 8860962 | 3 | 200512 | 200608 | 0 | |
| 88609627 | 8860962 | 4 | 20061110 | 20071104 | 0 | |
| 88609627 | 8860962 | 6 | 20041022 | 0 |