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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88609748 | 8860974 | 8 | F | 20050329 | 20160721 | 20121025 | 20160727 | EXP | US-009507513-1210USA005991 | MERCK | 0.00 | F | Y | 53.97000 | KG | 20160727 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88609748 | 8860974 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
| 88609748 | 8860974 | 2 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 0 | 70 | MG | /wk | |||||||
| 88609748 | 8860974 | 3 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 20560 | 70 | MG | TABLET | /wk | ||||||
| 88609748 | 8860974 | 4 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | U | 0 | ||||||||||
| 88609748 | 8860974 | 5 | C | VITAMINS (UNSPECIFIED) | VITAMINS | 1 | 1500 MG, UNK | U | 0 | 1500 | MG | ||||||||
| 88609748 | 8860974 | 6 | C | CALCIUM (UNSPECIFIED) | CALCIUM | 1 | 500 MG, UNK | U | 0 | 500 | MG | ||||||||
| 88609748 | 8860974 | 7 | C | VITAMIN D | CHOLECALCIFEROL | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88609748 | 8860974 | 1 | Osteoporosis |
| 88609748 | 8860974 | 2 | Osteoporosis |
| 88609748 | 8860974 | 3 | Osteoporosis |
| 88609748 | 8860974 | 4 | Systemic lupus erythematosus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 88609748 | 8860974 | OT |
| 88609748 | 8860974 | HO |
| 88609748 | 8860974 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88609748 | 8860974 | Anaemia postoperative | |
| 88609748 | 8860974 | Asthenia | |
| 88609748 | 8860974 | Bone loss | |
| 88609748 | 8860974 | Bronchitis | |
| 88609748 | 8860974 | Constipation | |
| 88609748 | 8860974 | Drug hypersensitivity | |
| 88609748 | 8860974 | Endodontic procedure | |
| 88609748 | 8860974 | Fall | |
| 88609748 | 8860974 | Fatigue | |
| 88609748 | 8860974 | Femur fracture | |
| 88609748 | 8860974 | Gastrooesophageal reflux disease | |
| 88609748 | 8860974 | Hyperlipidaemia | |
| 88609748 | 8860974 | Hypothyroidism | |
| 88609748 | 8860974 | Malaise | |
| 88609748 | 8860974 | Migraine | |
| 88609748 | 8860974 | Open reduction of fracture | |
| 88609748 | 8860974 | Oral surgery | |
| 88609748 | 8860974 | Osteoarthritis | |
| 88609748 | 8860974 | Peripheral swelling | |
| 88609748 | 8860974 | Radius fracture | |
| 88609748 | 8860974 | Rheumatoid arthritis | |
| 88609748 | 8860974 | Transfusion |
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 |
|---|---|---|---|---|---|---|
| 88609748 | 8860974 | 1 | 200007 | 200710 | 0 | |
| 88609748 | 8860974 | 2 | 20080417 | 201101 | 0 | |
| 88609748 | 8860974 | 3 | 20110110 | 201106 | 0 | |
| 88609748 | 8860974 | 4 | 199608 | 0 | ||
| 88609748 | 8860974 | 5 | 1999 | 0 | ||
| 88609748 | 8860974 | 6 | 1999 | 0 | ||
| 88609748 | 8860974 | 7 | 20050329 | 0 |