The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125169392 12516939 2 F 20160427 20160725 20160630 20160729 EXP GB-MHRA-ADR 23528966 GB-ACCORD-041874 ACCORD 0.00 F Y 0.00000 20160729 MD GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125169392 12516939 1 PS FLUOROURACIL. FLUOROURACIL 1 40743
125169392 12516939 2 SS EPIRUBICIN EPIRUBICIN 1 2147483647
125169392 12516939 3 SS CYCLOPHOSPHAMIDE/CYCLOPHOSPHAMIDE MONOHYDRATE CYCLOPHOSPHAMIDE 1 0
125169392 12516939 4 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 700 MG N 0 600 MG Q3W
125169392 12516939 5 SS TAXOTERE DOCETAXEL 1 0
125169392 12516939 6 C LETROZOLE. LETROZOLE 1 Oral 0 2.9 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125169392 12516939 1 Breast cancer
125169392 12516939 2 Breast cancer
125169392 12516939 3 Breast cancer
125169392 12516939 4 Breast cancer
125169392 12516939 5 Breast cancer
125169392 12516939 6 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125169392 12516939 HO
125169392 12516939 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125169392 12516939 Colitis
125169392 12516939 Colitis ulcerative
125169392 12516939 Malaise

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125169392 12516939 4 20150826 20160504 0
125169392 12516939 6 201510 0