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
5404427 5844455 F 2 5404427-0 20021107 20061113 20070711 PER 238339 NOVO NORDISK INC. 56 YR F N 81.6 KG 20070705 CN 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
5404427 1008768104 PS ACTIVELLA 1 ORAL 0.5 MG-1.0 MG, ORAL N D 20907
5404427 1008828866 SS PREMPRO 1 U U
5404427 1008828867 SS PREMARIN 1 0.9 MG N D
5404427 1008828869 SS PROVERA 1 U U
5404427 1008828873 SS ESTROGEN NOS (ESTROGENS NOS) 2 U U
5404427 1008828875 SS MEDROXYPROGESTERONE ACETATE 1 10 MG U U
5404427 1008828876 SS CENESTIN 1 1.25 MG N D
5404427 1008828877 C CELEXA (CITRALOPRAM HYDROBROMIDE) 2
5404427 1008828878 C PREVACID 1
5404427 1008828881 C MAXZIDE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5404427 1008768104 MENOPAUSAL SYMPTOMS
5404427 1008828866 MENOPAUSAL SYMPTOMS
5404427 1008828867 MENOPAUSAL SYMPTOMS
5404427 1008828869 MENOPAUSAL SYMPTOMS
5404427 1008828873 MENOPAUSAL SYMPTOMS
5404427 1008828875 MENOPAUSAL SYMPTOMS
5404427 1008828876 MENOPAUSAL SYMPTOMS

Outcome of event

Event ID OUTC COD
5404427 HO
5404427 OT
5404427 RI

Reactions reported

Event ID PT
5404427 BREAST CANCER

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

Event ID RPSR COD
5404427 CSM
5404427 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5404427 1008768104 20020930 20021111
5404427 1008828867 20000801 20010701
5404427 1008828875 20000801 20020628
5404427 1008828876 20010816 20020810