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
125398661 12539866 1 I 20090304 20090327 20160708 20160708 EXP PHHO2009FR018220 NOVARTIS 61.99 YR F Y 61.00000 KG 20160708 MD FR FR

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
125398661 12539866 1 PS TYKERB LAPATINIB DITOSYLATE 1 Oral 750 MG, QD 63000 MG Y 0 750 MG FILM-COATED TABLET QD
125398661 12539866 2 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) 100 MG/M2, CYCLIC 0 100 MG/M**2
125398661 12539866 3 SS TRASTUZUMAB TRASTUZUMAB 1 Intravenous (not otherwise specified) 4 MG/KG, QW Y 0 4 MG/KG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125398661 12539866 1 Breast cancer metastatic
125398661 12539866 2 Breast cancer metastatic
125398661 12539866 3 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
125398661 12539866 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125398661 12539866 Cardiac failure

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
125398661 12539866 1 20081211 20090330 0
125398661 12539866 2 20081211 0
125398661 12539866 3 20081211 0