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
83366022 8336602 2 F 200211 20160720 20120113 20160722 EXP US-ROCHE-1029432 ROCHE 51.48 YR F Y 0.00000 20160722 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
83366022 8336602 1 PS BONIVA IBANDRONATE SODIUM 1 Unknown U 21455
83366022 8336602 2 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown 0
83366022 8336602 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 70 MG
83366022 8336602 4 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 150 MG
83366022 8336602 5 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 70 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
83366022 8336602 1 Osteoporosis
83366022 8336602 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
83366022 8336602 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
83366022 8336602 Anxiety
83366022 8336602 Emotional distress
83366022 8336602 Femur fracture
83366022 8336602 Foot fracture
83366022 8336602 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
83366022 8336602 1 200603 200604 0
83366022 8336602 2 200106 0
83366022 8336602 3 20020221 0
83366022 8336602 4 200603 200612 0
83366022 8336602 5 20100115 0