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
86033342 8603334 2 F 20100113 20160823 20120607 20160824 EXP US-ROCHE-1074549 ROCHE 66.75 YR F Y 0.00000 20160824 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
86033342 8603334 1 PS BONIVA IBANDRONATE SODIUM 1 Oral 21455 150 MG TABLET
86033342 8603334 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 10 MG
86033342 8603334 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 0 70 MG
86033342 8603334 4 C PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 0
86033342 8603334 5 C RANITIDINE. RANITIDINE 1 Unknown 0
86033342 8603334 6 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86033342 8603334 1 Osteoporosis
86033342 8603334 2 Osteoporosis
86033342 8603334 5 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
86033342 8603334 HO
86033342 8603334 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86033342 8603334 Anxiety
86033342 8603334 Emotional distress
86033342 8603334 Femur 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
86033342 8603334 1 200706 201001 0
86033342 8603334 2 199709 200106 0
86033342 8603334 3 200106 200706 0
86033342 8603334 4 200612 200903 0
86033342 8603334 5 2009 0
86033342 8603334 6 200606 200905 0