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
127292531 12729253 1 I 201501 0 20160907 20160907 DIR FDA-CTU 58.94 YR F N 130.00000 LBS 20160907 N MD 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
127292531 12729253 1 PS ESTRADIOL. ESTRADIOL 1 D D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127292531 12729253 1 Atrophic vulvovaginitis
127292531 12729253 1 Burning mouth syndrome
127292531 12729253 1 Menopausal symptoms

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127292531 12729253 Drug ineffective
127292531 12729253 Product substitution issue

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

Event ID CASEID RPSR COD
127292531 12729253 HP

Therapies reported

no results found