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
126076221 12607622 1 I 20160718 20160729 20160729 PER US-BAYER-2016-141068 BAYER 55.00 YR A F Y 0.00000 20160729 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
126076221 12607622 1 PS CLIMARA ESTRADIOL 1 Transdermal 1 DF, OW 20375 1 DF TRANSDERMAL PATCH /wk
126076221 12607622 2 SS CLIMARA ESTRADIOL 1 Transdermal 1 DF, OW 150400 20375 1 DF TRANSDERMAL PATCH /wk
126076221 12607622 3 SS CLIMARA ESTRADIOL 1 Transdermal 1 DF, OW 150400 20375 1 DF TRANSDERMAL PATCH /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126076221 12607622 1 Oestradiol decreased
126076221 12607622 2 Oestradiol decreased
126076221 12607622 3 Oestradiol decreased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126076221 12607622 Frustration tolerance decreased
126076221 12607622 Intentional product misuse
126076221 12607622 Malaise
126076221 12607622 Product adhesion issue
126076221 12607622 Product quality issue

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
126076221 12607622 1 201605 201607 0
126076221 12607622 2 201607 0
126076221 12607622 3 20160718 0