The Safety Rates Drug Report

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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
85064593 8506459 3 F 201001 20160823 20120412 20160826 EXP US-ROCHE-1056652 ROCHE 78.64 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
85064593 8506459 1 PS BONIVA IBANDRONATE SODIUM 1 Unknown 21455
85064593 8506459 2 SS BONIVA IBANDRONATE SODIUM 1 21455
85064593 8506459 3 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown 0
85064593 8506459 4 SS FOSAMAX ALENDRONATE SODIUM 1 0
85064593 8506459 5 SS ALENDRONATE ALENDRONATE SODIUM 1 Unknown 0
85064593 8506459 6 SS ALENDRONATE ALENDRONATE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
85064593 8506459 1 Osteoporosis
85064593 8506459 2 Osteopenia
85064593 8506459 3 Osteoporosis
85064593 8506459 4 Osteopenia
85064593 8506459 5 Osteoporosis
85064593 8506459 6 Osteopenia

Outcome of event

Event ID CASEID OUTC COD
85064593 8506459 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
85064593 8506459 Anxiety
85064593 8506459 Femur fracture
85064593 8506459 Low turnover osteopathy

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
85064593 8506459 1 200312 200911 0
85064593 8506459 3 200312 200911 0
85064593 8506459 5 200312 200911 0