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
110897063 11089706 3 F 201202 20160817 20150505 20160826 PER US-BAYER-2015-183174 BAYER 21.00 YR A F Y 49.89000 KG 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
110897063 11089706 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
110897063 11089706 2 SS MIRENA LEVONORGESTREL 1 21225 INTRAUTERINE DELIVERY SYSTEM
110897063 11089706 3 C SPRINTEC ETHINYL ESTRADIOLNORGESTIMATE 1 0
110897063 11089706 4 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110897063 11089706 1 Contraception
110897063 11089706 2 Menorrhagia

Outcome of event

Event ID CASEID OUTC COD
110897063 11089706 LT
110897063 11089706 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
110897063 11089706 Abdominal pain lower
110897063 11089706 Drug ineffective
110897063 11089706 General physical health deterioration
110897063 11089706 Injury
110897063 11089706 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
110897063 11089706 1 20111221 20130612 0