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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100154918 | 10015491 | 8 | F | 200107 | 20160819 | 20140317 | 20160825 | EXP | US-009507513-1403USA005842 | MERCK | 0.00 | F | Y | 55.33000 | KG | 20160825 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100154918 | 10015491 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 16982.83 | MG | 20560 | 70 | MG | TABLET | /wk | ||||
| 100154918 | 10015491 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | UNK, UNKNOWN | 16982.83 | MG | 20560 | TABLET | |||||||
| 100154918 | 10015491 | 3 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 0 | 70 | MG | /wk | |||||||
| 100154918 | 10015491 | 4 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | 0 | ||||||||||||
| 100154918 | 10015491 | 5 | C | CALCIUM (UNSPECIFIED) | CALCIUM | 1 | Oral | 1000 MG, UNKNOWN | 0 | 1000 | MG | ||||||||
| 100154918 | 10015491 | 6 | C | ESTROGEN NOS | ESTROGENS | 1 | Oral | UNK, UNKNOWN | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 100154918 | 10015491 | 1 | Osteopenia |
| 100154918 | 10015491 | 2 | Osteoporosis prophylaxis |
| 100154918 | 10015491 | 3 | Osteopenia |
| 100154918 | 10015491 | 4 | Osteoporosis prophylaxis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 100154918 | 10015491 | OT |
| 100154918 | 10015491 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 100154918 | 10015491 | Arthralgia | |
| 100154918 | 10015491 | Bone disorder | |
| 100154918 | 10015491 | Contusion | |
| 100154918 | 10015491 | Fall | |
| 100154918 | 10015491 | Femur fracture | |
| 100154918 | 10015491 | Hyperlipidaemia | |
| 100154918 | 10015491 | Hypertension | |
| 100154918 | 10015491 | Impaired healing | |
| 100154918 | 10015491 | Large intestine polyp | |
| 100154918 | 10015491 | Medical device discomfort | |
| 100154918 | 10015491 | Medical device removal | |
| 100154918 | 10015491 | Muscle strain | |
| 100154918 | 10015491 | Muscular weakness | |
| 100154918 | 10015491 | Osteoarthritis | |
| 100154918 | 10015491 | Osteoporosis | |
| 100154918 | 10015491 | Pain | |
| 100154918 | 10015491 | Pharyngitis | |
| 100154918 | 10015491 | Seasonal allergy | |
| 100154918 | 10015491 | Seborrhoeic dermatitis | |
| 100154918 | 10015491 | Tooth extraction |
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 |
|---|---|---|---|---|---|---|
| 100154918 | 10015491 | 1 | 20010206 | 20090326 | 0 | |
| 100154918 | 10015491 | 2 | 2006 | 0 | ||
| 100154918 | 10015491 | 3 | 200807 | 20100212 | 0 | |
| 100154918 | 10015491 | 5 | 1999 | 0 | ||
| 100154918 | 10015491 | 6 | 1996 | 0 |