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
126585921 12658592 1 I 20160731 0 20160816 20160816 DIR 56.00 YR F N 130.00000 LBS 20160815 N COUNTRY NOT SPECIFIED

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
126585921 12658592 1 PS ACTONEL RISEDRONATE SODIUM 1 Oral 1 TABLET (S) MONTH TAKEN BY MOUTH N D 0 1 DF COATED TABLET
126585921 12658592 3 C CALTRATE 600 + D + MINERALS 2 0
126585921 12658592 5 C NATURE MADE FISH OIL 1200MG, 360MG OMEGA NATURE MADE NUITRITIONAL PRODUCT FISH OILOMEGA-3 FATTY ACIDS 1 0
126585921 12658592 7 C VITAMIN D3 CHOLECALCIFEROL 1 0
126585921 12658592 9 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126585921 12658592 1 Bone density increased
126585921 12658592 1 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126585921 12658592 Arthralgia
126585921 12658592 Back pain
126585921 12658592 Bone pain
126585921 12658592 Immobile
126585921 12658592 Quality of life decreased

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
126585921 12658592 1 20160612 20160710 0