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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103928638 | 10392863 | 8 | F | 1997 | 20160721 | 20140819 | 20160728 | EXP | US-009507513-1408USA005658 | MERCK | 0.00 | F | Y | 48.53000 | KG | 20160728 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103928638 | 10392863 | 1 | PS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | UNK | U | 20560 | TABLET | ||||||||
| 103928638 | 10392863 | 2 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | U | 20560 | 70 | MG | TABLET | /wk | |||||
| 103928638 | 10392863 | 3 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70/2800 MG QW | 0 | TABLET | /wk | ||||||||
| 103928638 | 10392863 | 4 | SS | FOSAMAX PLUS D | ALENDRONATE SODIUMCHOLECALCIFEROL | 1 | Oral | 70/2800 QW | 0 | TABLET | /wk | ||||||||
| 103928638 | 10392863 | 5 | SS | ALENDRONATE SODIUM. | ALENDRONATE SODIUM | 1 | Oral | 70 MG, QW | 0 | 70 | MG | /wk | |||||||
| 103928638 | 10392863 | 6 | C | VITAMINS (UNSPECIFIED) | VITAMINS | 1 | Unknown | 1 TABLET, QD | U | 0 | 1 | DF | QD | ||||||
| 103928638 | 10392863 | 7 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | 0.112 MG, QD | U | 0 | .112 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 103928638 | 10392863 | 1 | Osteoporosis |
| 103928638 | 10392863 | 3 | Osteoporosis |
| 103928638 | 10392863 | 5 | Osteoporosis |
| 103928638 | 10392863 | 6 | Product used for unknown indication |
| 103928638 | 10392863 | 7 | Hypothyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 103928638 | 10392863 | HO |
| 103928638 | 10392863 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 103928638 | 10392863 | Arthritis | |
| 103928638 | 10392863 | Blood thyroid stimulating hormone increased | |
| 103928638 | 10392863 | Body height decreased | |
| 103928638 | 10392863 | Breast cancer | |
| 103928638 | 10392863 | Calcium deficiency | |
| 103928638 | 10392863 | Dental prosthesis placement | |
| 103928638 | 10392863 | Facial paralysis | |
| 103928638 | 10392863 | Fall | |
| 103928638 | 10392863 | Femur fracture | |
| 103928638 | 10392863 | Hip arthroplasty | |
| 103928638 | 10392863 | Hyperlipidaemia | |
| 103928638 | 10392863 | Jaw disorder | |
| 103928638 | 10392863 | Joint stiffness | |
| 103928638 | 10392863 | Migraine with aura | |
| 103928638 | 10392863 | Packed red blood cell transfusion | |
| 103928638 | 10392863 | Pain in extremity | |
| 103928638 | 10392863 | Radiotherapy | |
| 103928638 | 10392863 | Sacroiliitis | |
| 103928638 | 10392863 | Scoliosis | |
| 103928638 | 10392863 | Seasonal allergy | |
| 103928638 | 10392863 | Spinal osteoarthritis | |
| 103928638 | 10392863 | Varicella | |
| 103928638 | 10392863 | Vertigo |
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 |
|---|---|---|---|---|---|---|
| 103928638 | 10392863 | 1 | 199509 | 0 | ||
| 103928638 | 10392863 | 2 | 20061120 | 20071119 | 0 | |
| 103928638 | 10392863 | 3 | 20071219 | 201002 | 0 | |
| 103928638 | 10392863 | 4 | 201011 | 2012 | 0 | |
| 103928638 | 10392863 | 5 | 201002 | 201011 | 0 | |
| 103928638 | 10392863 | 6 | 1994 | 0 | ||
| 103928638 | 10392863 | 7 | 1984 | 0 |