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
105714644 10571464 4 F 201201 20160816 20141107 20160826 PER US-BAYER-2014-163070 BAYER 25.00 YR A F Y 0.00000 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
105714644 10571464 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
105714644 10571464 2 C TYLENOL [DIPHENHYDRAMINE HYDROCHLORIDE,PARACETAMOL] ACETAMINOPHENDIPHENHYDRAMINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105714644 10571464 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
105714644 10571464 HO
105714644 10571464 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105714644 10571464 Cardiac disorder
105714644 10571464 Device issue
105714644 10571464 Injury
105714644 10571464 Lung disorder
105714644 10571464 Pain
105714644 10571464 Renal disorder
105714644 10571464 Salpingo-oophoritis
105714644 10571464 Septic shock
105714644 10571464 Uterine infection
105714644 10571464 Uterine perforation

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
105714644 10571464 1 201111 20120114 0