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
6770225 7429535 F 1 6770225-9 20030201 20090514 20100520 PER 2008053291 PFIZER INC 61 YR F N 69 KG 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
6770225 1013868518 PS PROVERA 1 ORAL , ORAL D D 11839
6770225 1013925550 SS MEDROXYPROGESTERONE ACETATE 1 ORAL , ORAL D D
6770225 1013925593 SS PREMARIN 1 D D
6770225 1013925634 SS PREMPRO 1 D D
6770225 1013925638 SS MEDROXYPROGESTERONE 1 D D
6770225 1013925642 SS PROMETRIUM 1 D D
6770225 1013925687 SS ESTRADIOL 1 D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6770225 1013868518 HORMONE REPLACEMENT THERAPY
6770225 1013925550 HORMONE REPLACEMENT THERAPY
6770225 1013925593 HORMONE REPLACEMENT THERAPY
6770225 1013925634 HORMONE REPLACEMENT THERAPY
6770225 1013925638 HORMONE REPLACEMENT THERAPY
6770225 1013925642 HORMONE REPLACEMENT THERAPY
6770225 1013925687 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6770225 OT

Reactions reported

Event ID PT
6770225 BREAST CANCER FEMALE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6770225 1013868518 19900101 20000701
6770225 1013925550 19900101 20021001
6770225 1013925593 19900101 20000101
6770225 1013925634 19900101 20021201
6770225 1013925638 19900101 20000701
6770225 1013925642 20021201 20030301
6770225 1013925687 20021201 20030301