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
6781099 7456512 F 1 6781099-4 20011101 20090521 20100520 PER 2008054109 PFIZER INC 51 YR F N 74 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
6781099 1013901714 PS PROVERA 1 ORAL ORAL D D 11839
6781099 1014051395 SS MEDROXYPROGESTERONE ACETATE 1 ORAL ORAL D D
6781099 1014051396 SS MEDROXYPROGESTERONE 1 D D
6781099 1014051399 SS PREMPHASE (PREMARIN;CYCRIN 14/14) 1 D D
6781099 1014051400 SS CYCRIN 1 D D
6781099 1014051401 SS PREMARIN 1 D D
6781099 1014051402 SS ORTHO-PREFEST (ESTRADIOL, NORGESTIMATE) 2 D D
6781099 1014051403 SS PREMPRO 1 D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6781099 1013901714 HORMONE REPLACEMENT THERAPY
6781099 1014051395 HORMONE REPLACEMENT THERAPY
6781099 1014051396 HORMONE REPLACEMENT THERAPY
6781099 1014051399 HORMONE REPLACEMENT THERAPY
6781099 1014051400 HORMONE REPLACEMENT THERAPY
6781099 1014051401 HORMONE REPLACEMENT THERAPY
6781099 1014051402 HORMONE REPLACEMENT THERAPY
6781099 1014051403 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6781099 OT

Reactions reported

Event ID PT
6781099 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
6781099 1013901714 19990701 20001101
6781099 1014051395 19990701 20001101
6781099 1014051396 19990701 20001101
6781099 1014051399 19971201 19980501
6781099 1014051400 19980601 19990801
6781099 1014051401 19980601 20001201
6781099 1014051402 20010301
6781099 1014051403 20010601 20011101