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
82810662 8281066 2 F 201002 20160720 20111208 20160726 EXP US-ROCHE-1018094 ROCHE 66.86 YR F Y 0.00000 20160726 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
82810662 8281066 1 PS BONIVA IBANDRONATE SODIUM 1 Unknown 21455 150 MG
82810662 8281066 2 SS BONIVA IBANDRONATE SODIUM 1 21455
82810662 8281066 3 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown 0 70 MG
82810662 8281066 4 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown 0
82810662 8281066 5 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Unknown U 0 70 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82810662 8281066 1 Osteoporosis
82810662 8281066 2 Osteitis deformans
82810662 8281066 3 Osteoporosis
82810662 8281066 4 Osteitis deformans
82810662 8281066 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
82810662 8281066 OT
82810662 8281066 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
82810662 8281066 Anxiety
82810662 8281066 Bone disorder
82810662 8281066 Depression
82810662 8281066 Emotional distress
82810662 8281066 Femur fracture
82810662 8281066 Foot fracture
82810662 8281066 Low turnover osteopathy
82810662 8281066 Stress fracture
82810662 8281066 Toxicity to various agents

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
82810662 8281066 1 200902 201003 0
82810662 8281066 3 200304 200802 0
82810662 8281066 4 200802 200902 0
82810662 8281066 5 200802 200809 0