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
89225712 8922571 2 F 200303 20160720 20121123 20160725 EXP US-ROCHE-1158780 ROCHE 51.66 YR F Y 0.00000 20160725 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
89225712 8922571 1 PS BONIVA IBANDRONATE SODIUM 1 Unknown U 21455
89225712 8922571 2 SS BONIVA IBANDRONATE SODIUM 1 U 21455
89225712 8922571 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral U 0
89225712 8922571 4 SS FOSAMAX ALENDRONATE SODIUM 1 U 0
89225712 8922571 5 SS RECLAST ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89225712 8922571 1 Osteoporosis
89225712 8922571 2 Bone loss
89225712 8922571 3 Osteoporosis
89225712 8922571 4 Bone loss
89225712 8922571 5 Bone loss

Outcome of event

Event ID CASEID OUTC COD
89225712 8922571 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89225712 8922571 Depression
89225712 8922571 Emotional distress
89225712 8922571 Femoral neck fracture
89225712 8922571 Femur fracture
89225712 8922571 Hip fracture
89225712 8922571 Low turnover osteopathy
89225712 8922571 Pelvic fracture
89225712 8922571 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
89225712 8922571 1 2007 2008 0
89225712 8922571 3 1998 2005 0
89225712 8922571 5 2009 0