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
6769455 7432152 F 1 6769455-1 20030416 20090702 20100520 PER 2008058878 PFIZER INC 60 YR F N 81 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
6769455 1013865535 PS PROVERA 1 ORAL ORAL D D 11839
6769455 1013935321 SS MEDROXYPROGESTERONE ACETATE 1 ORAL ORAL D D
6769455 1013935324 SS PREMPRO 1 D D
6769455 1013935327 SS ESTRACE 1 D D
6769455 1013935331 SS PROMETRIUM 1 D D
6769455 1013935333 SS ESTRADIOL 1 D D
6769455 1013935338 SS PREMARIN 1 D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6769455 1013865535 HORMONE REPLACEMENT THERAPY
6769455 1013935321 HORMONE REPLACEMENT THERAPY
6769455 1013935324 HORMONE REPLACEMENT THERAPY
6769455 1013935327 HORMONE REPLACEMENT THERAPY
6769455 1013935331 HORMONE REPLACEMENT THERAPY
6769455 1013935333 HORMONE REPLACEMENT THERAPY
6769455 1013935338 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6769455 OT

Reactions reported

Event ID PT
6769455 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
6769455 1013865535 19880803 19981202
6769455 1013935321 20000112 20011121
6769455 1013935324 19961111 19980310
6769455 1013935327 19980608 20010101
6769455 1013935331 19990105 19991005
6769455 1013935333 19990105 20030212
6769455 1013935338 19880803 20061222