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
105716553 10571655 3 F 201008 20160921 20141107 20160929 PER US-BAYER-2014-163108 BAYER 40.00 YR A F Y 0.00000 20160929 MD 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
105716553 10571655 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TU00BZ0 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
105716553 10571655 2 SS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 21225 20 UG INTRAUTERINE DELIVERY SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105716553 10571655 1 Contraception
105716553 10571655 2 Menorrhagia

Outcome of event

Event ID CASEID OUTC COD
105716553 10571655 OT
105716553 10571655 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
105716553 10571655 Abdominal pain lower
105716553 10571655 Abdominal pain upper
105716553 10571655 Device failure
105716553 10571655 Device issue
105716553 10571655 Injury
105716553 10571655 Menstrual disorder
105716553 10571655 Pain
105716553 10571655 Uterine perforation

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
105716553 10571655 1 201005 201202 0
105716553 10571655 2 20120229 20150713 0