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
88424093 8842409 3 F 20110105 20160909 20121016 20160914 EXP US-009507513-1210USA004449 MERCK 0.00 F Y 58.50000 KG 20160914 CN 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
88424093 8842409 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK 20560 70 MG TABLET
88424093 8842409 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 40 MG, QD 20560 40 MG TABLET QD
88424093 8842409 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Unknown 70 MG, UNK 0 70 MG
88424093 8842409 4 C CALCIUM (UNSPECIFIED) CALCIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88424093 8842409 1 Osteoporosis
88424093 8842409 3 Osteoporosis
88424093 8842409 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
88424093 8842409 HO
88424093 8842409 OT
88424093 8842409 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
88424093 8842409 Ankle fracture
88424093 8842409 Fall
88424093 8842409 Femur fracture
88424093 8842409 Intramedullary rod insertion
88424093 8842409 Low turnover osteopathy
88424093 8842409 Rheumatoid arthritis

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
88424093 8842409 1 200005 201004 0
88424093 8842409 3 200005 201004 0
88424093 8842409 4 1965 0