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
124738063 12473806 3 F 20141210 20160706 20160616 20160714 EXP PHHO2014AR018608 NOVARTIS 62.00 YR F Y 74.00000 KG 20160714 MD AR AR

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
124738063 12473806 1 PS TYKERB LAPATINIB DITOSYLATE 1 Oral 1500 MG, QD 363699.688 MG Y 0 1500 MG FILM-COATED TABLET QD
124738063 12473806 2 SS LETROZOLE. LETROZOLE 1 Oral 2.5 MG, QD 606.166016 MG Y 0 2.5 MG QD
124738063 12473806 3 C TRASTUZUMAB TRASTUZUMAB 1 Unknown UNK 0
124738063 12473806 4 SS ANTHRACYCLINES UNSPECIFIED INGREDIENT 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124738063 12473806 1 Breast cancer metastatic
124738063 12473806 2 Breast cancer metastatic
124738063 12473806 3 Product used for unknown indication
124738063 12473806 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124738063 12473806 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124738063 12473806 Ejection fraction decreased

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
124738063 12473806 1 20120530 20141223 0
124738063 12473806 2 20120530 20150123 0
124738063 12473806 3 20100304 20101126 0
124738063 12473806 4 20091126 20100128 0