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
6790590 7546917 F 1 6790590-6 20060501 20090625 20100520 PER 200859969 PFIZER INC 49 YR F N 64 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
6790590 1013937647 PS MEDROXYPROGESTERONE ACETATE 1 ORAL ORAL D D 11839
6790590 1014123371 SS PREMARIN 1 ORAL 0.625 MG, ORAL D D
6790590 1014123455 SS ORTHO-PREFEST (ESTRADIOL, NORGESTIMATE) 2 D D
6790590 1014123472 SS PREMPRO 1 0.45/1.5 MG D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6790590 1013937647 HORMONE REPLACEMENT THERAPY
6790590 1014123371 HORMONE REPLACEMENT THERAPY
6790590 1014123455 HORMONE REPLACEMENT THERAPY
6790590 1014123472 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6790590 OT

Reactions reported

Event ID PT
6790590 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
6790590 1014123371 19961201 19970601
6790590 1014123371 19990601 20010101
6790590 1014123455 20010101 20020101
6790590 1014123472 20020101 20070501