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
89137862 8913786 2 F 2011 20160927 20121116 20160929 EXP US-ROCHE-1155762 ROCHE 66.55 YR F Y 0.00000 20160929 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
89137862 8913786 1 PS BONIVA IBANDRONATE SODIUM 1 Unknown 21455 150 MG
89137862 8913786 2 SS BONIVA IBANDRONATE SODIUM 1 21455
89137862 8913786 3 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown D 0 70 MG
89137862 8913786 4 SS FOSAMAX ALENDRONATE SODIUM 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89137862 8913786 1 Osteoporosis
89137862 8913786 2 Osteopenia
89137862 8913786 3 Osteoporosis
89137862 8913786 4 Osteopenia

Outcome of event

Event ID CASEID OUTC COD
89137862 8913786 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89137862 8913786 Anxiety
89137862 8913786 Emotional distress
89137862 8913786 Femur fracture
89137862 8913786 Low turnover osteopathy
89137862 8913786 Radius 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
89137862 8913786 1 20090428 20110131 0
89137862 8913786 3 200509 200812 0