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
86718293 8671829 3 F 20030602 20160720 20120718 20160728 EXP US-009507513-1207USA003753 MERCK 0.00 F Y 0.00000 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
86718293 8671829 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 10 MG, UNK 20560 10 MG TABLET
86718293 8671829 2 SS FOSAMAX ALENDRONATE SODIUM 1 20560 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86718293 8671829 1 Osteopenia
86718293 8671829 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
86718293 8671829 OT
86718293 8671829 HO
86718293 8671829 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
86718293 8671829 Abdominal pain
86718293 8671829 Chronic obstructive pulmonary disease
86718293 8671829 Death
86718293 8671829 Dehydration
86718293 8671829 Device breakage
86718293 8671829 Fall
86718293 8671829 Femur fracture
86718293 8671829 Fracture nonunion
86718293 8671829 Low turnover osteopathy
86718293 8671829 Pain in extremity
86718293 8671829 Peptic ulcer
86718293 8671829 Shock

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
86718293 8671829 1 20030128 20090303 0