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
126035471 12603547 1 I 20160722 20160728 20160728 EXP 2016-001543 WARNER CHILCOTT JOURNAL: OSTEOPOROS INT?AUTHOR: UGURLAR M?TITLE: ALENDRONATE- AND RISEDRONATE-INDUCED ACUTE POLYARTHRITIS?VOLUME: EPUB YEAR: 2016 PAGES: EPUB 52.00 YR F Y 0.00000 20160728 OT TR TR

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
126035471 12603547 1 PS ACTONEL RISEDRONATE SODIUM 1 Oral Y 20835 35 MG TABLET
126035471 12603547 2 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral Y 0 70 MG
126035471 12603547 3 C CALCIUM CALCIUM 1 0
126035471 12603547 4 C VITAMIN D3DIETARY SUPPLEMEN DIETARY SUPPLEMENT ALPHA-TOCOPHEROLCHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126035471 12603547 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
126035471 12603547 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126035471 12603547 Arthralgia
126035471 12603547 Joint effusion
126035471 12603547 Joint range of motion decreased
126035471 12603547 Joint swelling
126035471 12603547 Joint warmth
126035471 12603547 Myalgia
126035471 12603547 Polyarthritis
126035471 12603547 Synovitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found