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
122186922 12218692 2 F 201603 20160713 20160329 20160725 PER US-BAYER-2016-058673 BAYER 28.00 YR A F Y 87.98000 KG 20160725 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
122186922 12218692 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TU00FEZ 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
122186922 12218692 2 SS MIRENA LEVONORGESTREL 1 21225 INTRAUTERINE DELIVERY SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122186922 12218692 1 Contraception
122186922 12218692 2 Menorrhagia

Outcome of event

Event ID CASEID OUTC COD
122186922 12218692 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122186922 12218692 Device difficult to use
122186922 12218692 Device dislocation
122186922 12218692 Drug ineffective
122186922 12218692 Haemorrhage in pregnancy
122186922 12218692 Pregnancy with contraceptive device

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
122186922 12218692 1 20120815 0