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
125238402 12523840 2 F 20160427 20160725 20160704 20160805 EXP GB-CIPLA LTD.-2016GB08171 CIPLA 0.00 Y 0.00000 20160805 OT 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
125238402 12523840 1 PS Epirubicin EPIRUBICIN 1 Unknown UNK 65361
125238402 12523840 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown UNK 0
125238402 12523840 3 SS FLUOROURACIL. FLUOROURACIL 1 Unknown UNK 0
125238402 12523840 4 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, ONCE THREE WEEKLY 7000 MG U U 0 600 MG
125238402 12523840 5 SS TAXOTERE DOCETAXEL 1 Unknown UNK 0
125238402 12523840 6 C LETROZOLE. LETROZOLE 1 Oral 2.9 MG, QD U U 0 2.9 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125238402 12523840 1 Breast cancer
125238402 12523840 2 Breast cancer
125238402 12523840 3 Breast cancer
125238402 12523840 4 Breast cancer
125238402 12523840 5 Breast cancer
125238402 12523840 6 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125238402 12523840 OT
125238402 12523840 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125238402 12523840 Colitis
125238402 12523840 Colitis ulcerative
125238402 12523840 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
125238402 12523840 4 20150826 20160504 0
125238402 12523840 6 201510 0