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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 78896628 | 7889662 | 8 | F | 20030407 | 20160908 | 20110407 | 20160914 | EXP | US-009507513-1103USA03950 | MERCK | 0.00 | F | Y | 69.40000 | KG | 20160914 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 78896628 | 7889662 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | UNK | 20560 | TABLET | |||||||||
| 78896628 | 7889662 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | UNK UNK, QW | 20560 | TABLET | /wk | ||||||||
| 78896628 | 7889662 | 3 | C | CENTRUM SILVER | MINERALSVITAMINS | 1 | Unknown | U | 0 | ||||||||||
| 78896628 | 7889662 | 4 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70MG/2800IU,QW | 0 | TABLET | |||||||||
| 78896628 | 7889662 | 5 | C | CALCIUM (UNSPECIFIED) | CALCIUM | 1 | Unknown | UNK, QD | U | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 78896628 | 7889662 | 1 | Osteoporosis |
| 78896628 | 7889662 | 3 | Product used for unknown indication |
| 78896628 | 7889662 | 4 | Osteoporosis |
| 78896628 | 7889662 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 78896628 | 7889662 | DS |
| 78896628 | 7889662 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 78896628 | 7889662 | Actinic keratosis | |
| 78896628 | 7889662 | Adverse drug reaction | |
| 78896628 | 7889662 | Arthritis | |
| 78896628 | 7889662 | Back pain | |
| 78896628 | 7889662 | Basal cell carcinoma | |
| 78896628 | 7889662 | Blood creatinine increased | |
| 78896628 | 7889662 | Bone disorder | |
| 78896628 | 7889662 | Breast pain | |
| 78896628 | 7889662 | Bronchitis | |
| 78896628 | 7889662 | Cardiac murmur | |
| 78896628 | 7889662 | Carpal tunnel syndrome | |
| 78896628 | 7889662 | Cataract | |
| 78896628 | 7889662 | Constipation | |
| 78896628 | 7889662 | Extrasystoles | |
| 78896628 | 7889662 | Fall | |
| 78896628 | 7889662 | Femur fracture | |
| 78896628 | 7889662 | Haemorrhoid operation | |
| 78896628 | 7889662 | Hypercalcaemia | |
| 78896628 | 7889662 | Hyperlipidaemia | |
| 78896628 | 7889662 | Inappropriate schedule of drug administration | |
| 78896628 | 7889662 | Muscle rupture | |
| 78896628 | 7889662 | Nausea | |
| 78896628 | 7889662 | Neoplasm malignant | |
| 78896628 | 7889662 | Nocturia | |
| 78896628 | 7889662 | Osteoarthritis | |
| 78896628 | 7889662 | Osteopenia | |
| 78896628 | 7889662 | Pain in extremity | |
| 78896628 | 7889662 | Papule | |
| 78896628 | 7889662 | Retinal detachment | |
| 78896628 | 7889662 | Sarcoma | |
| 78896628 | 7889662 | Sialoadenitis | |
| 78896628 | 7889662 | Squamous cell carcinoma | |
| 78896628 | 7889662 | Squamous cell carcinoma of skin | |
| 78896628 | 7889662 | Stress fracture | |
| 78896628 | 7889662 | Tendonitis | |
| 78896628 | 7889662 | Tooth disorder | |
| 78896628 | 7889662 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 78896628 | 7889662 | 1 | 2000 | 201003 | 0 | |
| 78896628 | 7889662 | 2 | 20080109 | 0 | ||
| 78896628 | 7889662 | 4 | 200702 | 0 |