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
6769457 7432151 F 1 6769457-5 20000216 20090618 20100520 PER 2008058879 PFIZER INC 57 YR F N 52 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
6769457 1013865539 PS MEDROXYPROGESTERONE ACETATE 1 ORAL ORAL D D 11839
6769457 1013935407 SS PREMPRO 1 D D
6769457 1013935424 SS ESTRADIOL 1 D D
6769457 1013935430 SS ESTRADERM 1 D D
6769457 1013935431 C SYNTHROID 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6769457 1013865539 HORMONE REPLACEMENT THERAPY
6769457 1013935407 HORMONE REPLACEMENT THERAPY
6769457 1013935424 HORMONE REPLACEMENT THERAPY
6769457 1013935430 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6769457 OT

Reactions reported

Event ID PT
6769457 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
6769457 1013865539 19980512 19990209
6769457 1013935407 19991018
6769457 1013935424 19980512 19990209
6769457 1013935430 19980101