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
5041729 5988025 F 3 5041729-4 19981008 20060619 20060630 EXP HQWYE684024NOV04 WYETH PHARMACEUTICALS INC. 53 YR F N 70.37 KG 20060629 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
5041729 1007435628 PS PREMPRO 1 ORAL 0.625 MG, ORAL D D 20527
5041729 1007457206 SS PREMARIN 1 ORAL ORAL D D
5041729 1007457207 SS PROVERA 1 ORAL ORAL D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
5041729 1007435628 OSTEOPOROSIS
5041729 1007435628 PROPHYLAXIS
5041729 1007457206 MENOPAUSE
5041729 1007457207 MENOPAUSE

Outcome of event

Event ID OUTC COD
5041729 HO
5041729 OT

Reactions reported

Event ID PT
5041729 BREAST CANCER FEMALE
5041729 BREAST CANCER IN SITU
5041729 BREAST MICROCALCIFICATION
5041729 CONTRALATERAL BREAST CANCER
5041729 DEPRESSION
5041729 POST PROCEDURAL PULMONARY EMBOLISM
5041729 PROGESTERONE RECEPTOR ASSAY POSITIVE
5041729 SURGICAL PROCEDURE REPEATED
5041729 VENOUS THROMBOSIS LIMB

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

Event ID RPSR COD
5041729 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5041729 1007435628 19990701 20001101
5041729 1007457206 19900101 19980101
5041729 1007457207 19900101 19980101