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
6783927 7460278 F 1 6783927-5 20000101 20080711 20100520 PER 2008062488 PFIZER INC YR F N 20100405 LW 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
6783927 1013913266 PS MEDROXYPROGESTERONE ACETATE 1 ORAL ORAL D D 11839
6783927 1014067905 SS PREMPRO 1 D D
6783927 1014067906 SS PREMARIN 1 D D
6783927 1014067907 SS CYCRIN 1 D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6783927 1013913266 HORMONE REPLACEMENT THERAPY
6783927 1014067905 HORMONE REPLACEMENT THERAPY
6783927 1014067906 HORMONE REPLACEMENT THERAPY
6783927 1014067907 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6783927 OT

Reactions reported

Event ID PT
6783927 BREAST CANCER FEMALE

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

Event ID RPSR COD
6783927 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6783927 1013913266 19990901 19991201
6783927 1014067905 19960101 19990101
6783927 1014067906 19990601 19991201
6783927 1014067907 19990601 19991201