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
84976983 8497698 3 F 201002 20160823 20120406 20160825 EXP US-ROCHE-1056675 ROCHE 86.43 YR F Y 0.00000 20160825 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
84976983 8497698 1 PS BONIVA IBANDRONATE SODIUM 1 Oral 21455 TABLET
84976983 8497698 2 SS BONIVA IBANDRONATE SODIUM 1 Oral 21455 150 MG TABLET
84976983 8497698 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0
84976983 8497698 4 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 70 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
84976983 8497698 1 Osteoporosis
84976983 8497698 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
84976983 8497698 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
84976983 8497698 Anxiety
84976983 8497698 Depression
84976983 8497698 Emotional distress
84976983 8497698 Facial bones fracture
84976983 8497698 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
84976983 8497698 1 20051031 0
84976983 8497698 2 200510 200802 0
84976983 8497698 3 20040206 0
84976983 8497698 4 200302 200509 0