The Safety Rates Drug Report

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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
121702262 12170226 2 F 20160226 20160708 20160311 20160713 PER PHEH2016US005742 NOVARTIS 83.84 YR F Y 0.00000 20160713 CN US US

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
121702262 12170226 1 PS TYKERB LAPATINIB DITOSYLATE 1 Oral 750 MG, QD (3 TABLETS) 5ZP1656 22059 750 MG TABLET QD
121702262 12170226 2 C METOPROLOL. METOPROLOL 1 Unknown UNK U 0 EXTENDED RELEASE TABLET
121702262 12170226 3 C PROCHLORPERAZ PROCHLORPERAZINE MALEATE 1 Unknown UNK U 0 TABLET
121702262 12170226 4 C SIMVASTATIN. SIMVASTATIN 1 Unknown UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121702262 12170226 1 Breast cancer female
121702262 12170226 2 Product used for unknown indication
121702262 12170226 3 Product used for unknown indication
121702262 12170226 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121702262 12170226 Diarrhoea
121702262 12170226 Fatigue
121702262 12170226 Rash

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
121702262 12170226 1 20160226 0