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
77959872 7795987 2 F 200501 20160720 20110202 20160727 EXP US-ROCHE-755939 ROCHE 0.00 F Y 0.00000 20160727 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
77959872 7795987 1 PS BONIVA IBANDRONATE SODIUM 1 Oral U 21455 TABLET
77959872 7795987 2 SS BONIVA IBANDRONATE SODIUM 1 Oral U 21455 150 MG TABLET
77959872 7795987 3 SS ACTONEL RISEDRONATE SODIUM 1 Unknown U 0
77959872 7795987 4 SS FOSAMAX ALENDRONATE SODIUM 1 Oral U 0 70 MG
77959872 7795987 5 C CYCLOBENZAPRINE CYCLOBENZAPRINE 1 Unknown 0
77959872 7795987 6 C FORTEO TERIPARATIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77959872 7795987 1 Osteoporosis
77959872 7795987 3 Osteoporosis
77959872 7795987 4 Osteoporosis
77959872 7795987 5 Pain
77959872 7795987 6 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
77959872 7795987 OT
77959872 7795987 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
77959872 7795987 Ankle fracture
77959872 7795987 Anxiety
77959872 7795987 Depression
77959872 7795987 Emotional distress
77959872 7795987 Femur fracture
77959872 7795987 Foot fracture
77959872 7795987 Low turnover osteopathy
77959872 7795987 Pelvic fracture
77959872 7795987 Wrist 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
77959872 7795987 1 200608 201001 0
77959872 7795987 3 200508 200608 0
77959872 7795987 4 200402 200508 0
77959872 7795987 5 2005 2010 0