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
105716412 10571641 2 F 2013 20160803 20141107 20160815 PER US-BAYER-2014-163188 BAYER 36.00 YR A F Y 0.00000 20160815 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
105716412 10571641 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, UNK TU00D8L 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
105716412 10571641 2 C DOXY [DOXYCYCLINE] 2 0
105716412 10571641 3 C FLAGYL METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105716412 10571641 1 Contraception
105716412 10571641 2 Infection
105716412 10571641 3 Infection

Outcome of event

Event ID CASEID OUTC COD
105716412 10571641 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105716412 10571641 Anxiety
105716412 10571641 Depression
105716412 10571641 Device difficult to use
105716412 10571641 Drug ineffective
105716412 10571641 Embedded device
105716412 10571641 Emotional distress
105716412 10571641 Injury
105716412 10571641 Medical device discomfort
105716412 10571641 Medical device pain
105716412 10571641 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
105716412 10571641 1 20120828 0