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
100722843 10072284 3 F 20110126 20160817 20140411 20160826 PER US-BAYER-2014-052886 BAYER 36.00 YR A F Y 52.15000 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
100722843 10072284 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT Y 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
100722843 10072284 2 C PRENATAL VITAMINS 1 UNK 0
100722843 10072284 3 C TYLENOL ACETAMINOPHEN 1 0
100722843 10072284 4 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100722843 10072284 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
100722843 10072284 HO
100722843 10072284 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100722843 10072284 Abdominal pain lower
100722843 10072284 Anxiety
100722843 10072284 Depression
100722843 10072284 Device dislocation
100722843 10072284 Device issue
100722843 10072284 Emotional distress
100722843 10072284 Uterine perforation
100722843 10072284 Vulvovaginal 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
100722843 10072284 1 20110126 20110211 0
100722843 10072284 2 20081102 0