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
126203631 12620363 1 I 20160620 20160803 20160803 EXP GB-BAXTER-2016BAX032963 BAXTER 0.00 F Y 0.00000 20160803 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
126203631 12620363 1 PS CYCLOPHOSPHAMIDE INJECTION 1G CYCLOPHOSPHAMIDE 1 Unknown 13 CYCLES U 12142 POWDER FOR SOLUTION FOR INJECTION /cycle
126203631 12620363 2 SS epirubicin EPIRUBICIN 1 Unknown 13 CYCLES U 0 /cycle
126203631 12620363 3 SS FLUOROURACIL. FLUOROURACIL 1 Unknown 13 CYCLES U 0 /cycle
126203631 12620363 4 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 13 CYCLES U U 0 600 MG Q3W
126203631 12620363 5 SS TAXOTERE DOCETAXEL 1 Unknown 13 CYCLES U 0 /cycle
126203631 12620363 6 SS LETROZOLE. LETROZOLE 1 Oral U 0 2.9 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126203631 12620363 1 Breast cancer
126203631 12620363 2 Breast cancer
126203631 12620363 3 Breast cancer
126203631 12620363 4 Breast cancer
126203631 12620363 5 Breast cancer
126203631 12620363 6 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
126203631 12620363 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126203631 12620363 Colitis ulcerative
126203631 12620363 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
126203631 12620363 4 20150826 20160504 0
126203631 12620363 6 201510 0