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
125865001 12586500 1 I 20160618 20160718 20160722 20160722 EXP DL2016-0249 DANCO 26.00 YR F N 0.00000 20160719 N OT 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
125865001 12586500 1 PS MIFEPRISTONE TABLETS, 200 MG (DANCO LABS) MIFEPRISTONE 1 Oral D D 13015001603 20181031 0 200 MG
125865001 12586500 2 SS MISOPROSTOL TABLETS, 200 MCG MISOPROSTOL 1 Buccal D D 0 800 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125865001 12586500 1 Abortion induced

Outcome of event

Event ID CASEID OUTC COD
125865001 12586500 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125865001 12586500 Abortion incomplete
125865001 12586500 Haemoglobin decreased
125865001 12586500 Hysterectomy
125865001 12586500 Placenta accreta
125865001 12586500 Uterine haemorrhage

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
125865001 12586500 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125865001 12586500 1 20160610 0
125865001 12586500 2 20160611 0