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
105713834 10571383 4 F 200803 20160712 20141107 20160722 PER US-BAYER-2014-162715 BAYER 37.00 YR A F Y 0.00000 20160722 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
105713834 10571383 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20MCG/24HR,CONT 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
105713834 10571383 2 SS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TU009KN 21225 20 UG INTRAUTERINE DELIVERY SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105713834 10571383 1 Menorrhagia
105713834 10571383 2 Menorrhagia

Outcome of event

Event ID CASEID OUTC COD
105713834 10571383 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
105713834 10571383 Device difficult to use
105713834 10571383 Device failure
105713834 10571383 Device issue
105713834 10571383 Embedded device
105713834 10571383 Injury
105713834 10571383 Pain

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
105713834 10571383 1 20070418 20080313 0
105713834 10571383 2 20120525 20131205 0