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
110901603 11090160 3 F 201101 20160817 20150505 20160826 PER US-BAYER-2015-189234 BAYER 26.00 YR A F Y 72.56000 KG 20160826 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
110901603 11090160 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT N TU0065W 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
110901603 11090160 2 C PRENATAL VITAMINS VITAMINS 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110901603 11090160 1 Contraception
110901603 11090160 2 Nausea

Outcome of event

Event ID CASEID OUTC COD
110901603 11090160 LT
110901603 11090160 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
110901603 11090160 Abdominal pain
110901603 11090160 Abdominal pain lower
110901603 11090160 Alopecia
110901603 11090160 Anhedonia
110901603 11090160 Anxiety
110901603 11090160 Device issue
110901603 11090160 Emotional distress
110901603 11090160 Fear
110901603 11090160 General physical health deterioration
110901603 11090160 Injury
110901603 11090160 Menorrhagia
110901603 11090160 Pharmacophobia
110901603 11090160 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
110901603 11090160 1 20110103 20120918 0
110901603 11090160 2 2010 2013 0