The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6772793 7444875 F 1 6772793-X 20000929 20080623 20100520 PER 2008052212 PFIZER INC YR F N 20100405 UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6772793 1013879204 PS PROVERA 1 ORAL ORAL D D 11839
6772793 1013993864 SS MEDROXYPROGESTERONE ACETATE 1 ORAL ORAL D D
6772793 1013993908 SS PREMARIN 1 D D
6772793 1013993966 SS PREMPRO 1 D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6772793 1013879204 HORMONE REPLACEMENT THERAPY
6772793 1013993864 HORMONE REPLACEMENT THERAPY
6772793 1013993908 HORMONE REPLACEMENT THERAPY
6772793 1013993966 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6772793 OT

Reactions reported

Event ID PT
6772793 BREAST CANCER FEMALE

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

Event ID RPSR COD
6772793 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6772793 1013879204 19980101 20000901
6772793 1013993864 19980101 20000901
6772793 1013993908 19980101 20000901
6772793 1013993966 19980101 20000901