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
122234404 12223440 4 F 2014 20160726 20160330 20160728 EXP US-BAYER-2016-060339 BAYER 27.00 YR A F Y 61.68000 KG 20160728 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
122234404 12223440 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TUOOGP9 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
122234404 12223440 2 C CRYSELLE ETHINYL ESTRADIOLNORGESTREL 1 UNK 0
122234404 12223440 3 C KEFLEX CEPHALEXIN 1 0
122234404 12223440 4 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 0
122234404 12223440 5 C MOTRIN IBUPROFEN 1 0
122234404 12223440 6 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
122234404 12223440 7 C LO/OVRAL ETHINYL ESTRADIOLNORGESTREL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122234404 12223440 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
122234404 12223440 OT
122234404 12223440 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122234404 12223440 Abdominal pain lower
122234404 12223440 Device expulsion
122234404 12223440 Drug ineffective
122234404 12223440 Ectopic pregnancy with contraceptive device
122234404 12223440 Haemorrhage in pregnancy
122234404 12223440 Procedural pain
122234404 12223440 Salpingectomy

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
122234404 12223440 1 20130322 20140312 0
122234404 12223440 2 201403 201502 0