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
86843912 8684391 2 F 20090714 20160823 20120726 20160826 EXP US-ROCHE-1092033 ROCHE 78.97 YR F Y 0.00000 20160826 LW 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
86843912 8684391 1 PS BONIVA IBANDRONATE SODIUM 1 Unknown 21455
86843912 8684391 2 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown 0
86843912 8684391 3 SS ACTONEL RISEDRONATE SODIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86843912 8684391 1 Osteoporosis
86843912 8684391 2 Osteoporosis
86843912 8684391 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
86843912 8684391 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86843912 8684391 Anxiety
86843912 8684391 Emotional distress
86843912 8684391 Femur fracture

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
86843912 8684391 1 1999 20090714 0
86843912 8684391 2 1999 20090714 0
86843912 8684391 3 1999 2009 0