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
100137124 10013712 4 F 2011 20140929 20140316 20140930 PER US-BAYER-2014-037253 BAYER 24.00 YR A F Y 81.63000 KG 20140930 N OT 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
100137124 10013712 1 PS MIRENA LEVONORGESTREL 1 INTRAUTERINE 20 MCG/24HR, CONT D TU00076 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
100137124 10013712 2 SS MIRENA LEVONORGESTREL 1 INTRAUTERINE 20 MCG/24HR, CONT D TU00076 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
100137124 10013712 3 C CELEXA CITALOPRAM HYDROBROMIDE 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100137124 10013712 1 Contraception
100137124 10013712 2 Contraception

Outcome of event

Event ID CASEID OUTC COD
100137124 10013712 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100137124 10013712 Depression
100137124 10013712 Device dislocation
100137124 10013712 Device issue
100137124 10013712 Drug ineffective
100137124 10013712 Embedded device
100137124 10013712 Emotional distress
100137124 10013712 Injury
100137124 10013712 Pain
100137124 10013712 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
100137124 10013712 1 20090501 20111001 0
100137124 10013712 2 20090623 20110811 0