The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
102185706 10218570 6 F 20070108 20160727 20140605 20160729 EXP US-009507513-1406USA002204 MERCK 0.00 F Y 59.41000 KG 20160729 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
102185706 10218570 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
102185706 10218570 2 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral U 20560 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102185706 10218570 1 Osteoporosis
102185706 10218570 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
102185706 10218570 HO
102185706 10218570 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102185706 10218570 Arthropathy
102185706 10218570 Bone lesion
102185706 10218570 Bursitis
102185706 10218570 Cerebrovascular accident
102185706 10218570 Femur fracture
102185706 10218570 Gallbladder disorder
102185706 10218570 Hypertension
102185706 10218570 Hypothyroidism
102185706 10218570 Intramedullary rod insertion
102185706 10218570 Joint effusion
102185706 10218570 Low turnover osteopathy
102185706 10218570 Osteopenia
102185706 10218570 Osteoporosis
102185706 10218570 Rheumatoid arthritis

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
102185706 10218570 1 200001 201204 0