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
124898882 12489888 2 F 201605 20160628 20160622 20160707 PER US-BAYER-2016-118694 BAYER 53.00 YR A F Y 0.00000 20160707 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
124898882 12489888 1 PS CLIMARA ESTRADIOL 1 Transdermal 0.037 MG, UNK 150217 20375 .037 MG TRANSDERMAL PATCH
124898882 12489888 2 C DULOXETINE. DULOXETINE 1 60 MG, UNK 0 60 MG
124898882 12489888 3 C ALPRAZOLAM. ALPRAZOLAM 1 1 MG, UNK 0 1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124898882 12489888 2 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124898882 12489888 Application site erythema
124898882 12489888 Application site pruritus
124898882 12489888 Application site rash
124898882 12489888 Product adhesion issue
124898882 12489888 Product quality issue
124898882 12489888 Product shape issue
124898882 12489888 Rash papular
124898882 12489888 Rash pruritic

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
124898882 12489888 1 201605 0