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
125081662 12508166 2 F 20160427 20160725 20160629 20160803 EXP GB-PFIZER INC-2016309347 PFIZER 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
125081662 12508166 1 PS EPIRUBICIN HCL EPIRUBICIN HYDROCHLORIDE 1 UNK 50778
125081662 12508166 2 SS FLUOROURACIL. FLUOROURACIL 1 UNK 0
125081662 12508166 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK 0
125081662 12508166 4 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, ONCE IN 3 WEEKS 7584 MG N 0 600 MG Q3W
125081662 12508166 5 SS TAXOTERE DOCETAXEL 1 UNK 0
125081662 12508166 6 C LETROZOLE. LETROZOLE 1 Oral 2.9 MG, DAILY 0 2.9 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125081662 12508166 1 Breast cancer
125081662 12508166 2 Breast cancer
125081662 12508166 3 Breast cancer
125081662 12508166 4 Breast cancer
125081662 12508166 5 Breast cancer
125081662 12508166 6 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125081662 12508166 HO
125081662 12508166 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125081662 12508166 Colitis
125081662 12508166 Colitis ulcerative
125081662 12508166 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
125081662 12508166 4 20150826 20160504 0
125081662 12508166 6 201510 0