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
6779296 7454318 F 1 6779296-7 20030501 20090429 20100520 PER 2008058715 PFIZER INC 56 YR F N 58 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
6779296 1013894413 PS PROVERA 1 ORAL 2.5 MG, ORAL D D 11839
6779296 1014038922 SS PREMARIN 1 D D
6779296 1014039019 SS PREMPRO 1 0.625/MG D D
6779296 1014039021 SS ESTRATEST 1 D D
6779296 1014039022 SS COMBIPATCH 1 D D
6779296 1014039043 SS CYCRIN 1 2.5 MG D D
6779296 1014039130 C TRAZODONE HCL 1
6779296 1014039157 C ZOLOFT 1
6779296 1014039183 C APAP (PARACETAMOL) 2
6779296 1014039234 C HYDROCODONE BITARTRATE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6779296 1013894413 HORMONE REPLACEMENT THERAPY
6779296 1014038922 HORMONE REPLACEMENT THERAPY
6779296 1014039019 HORMONE REPLACEMENT THERAPY
6779296 1014039021 HORMONE REPLACEMENT THERAPY
6779296 1014039022 HORMONE REPLACEMENT THERAPY
6779296 1014039043 HORMONE REPLACEMENT THERAPY

Outcome of event

Event ID OUTC COD
6779296 HO
6779296 OT

Reactions reported

Event ID PT
6779296 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
6779296 1013894413 19970116 19990526
6779296 1014038922 19970101 19970211
6779296 1014039019 19960211 20020801
6779296 1014039021 19990120 19990721
6779296 1014039022 20020801 20030610
6779296 1014039043 19990421 19990721