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
78676453 7867645 3 F 20100302 20160624 20110323 20160701 EXP US-ROCHE-765667 ROCHE 66.13 YR F Y 0.00000 20160701 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
78676453 7867645 1 PS BONIVA IBANDRONATE SODIUM 1 Oral 21455 150 MG TABLET /month
78676453 7867645 2 SS BONIVA IBANDRONATE SODIUM 1 Oral 21455 150 MG /month
78676453 7867645 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 70 MG TABLET /wk
78676453 7867645 4 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 70 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
78676453 7867645 1 Osteopenia
78676453 7867645 3 Osteopenia

Outcome of event

Event ID CASEID OUTC COD
78676453 7867645 HO
78676453 7867645 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
78676453 7867645 Anxiety
78676453 7867645 Femur fracture
78676453 7867645 Low turnover osteopathy
78676453 7867645 Osteonecrosis of jaw

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
78676453 7867645 1 200611 200806 0
78676453 7867645 2 200811 201003 0
78676453 7867645 3 200106 200610 0
78676453 7867645 4 200807 200811 0