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
123467782 12346778 2 F 201406 20160704 20160509 20160706 EXP PHHY2016PL062693 NOVARTIS 52.00 YR F Y 0.00000 20160706 CN COUNTRY NOT SPECIFIED PL

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
123467782 12346778 1 PS TYVERB LAPATINIB 1 Unknown 22059
123467782 12346778 2 SS CAPECITABINE. CAPECITABINE 1 Unknown UNK 0
123467782 12346778 3 SS CAPECITABINE. CAPECITABINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123467782 12346778 1 Breast cancer
123467782 12346778 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
123467782 12346778 OT
123467782 12346778 DE
123467782 12346778 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123467782 12346778 Breast cancer
123467782 12346778 Death
123467782 12346778 Lupus-like syndrome
123467782 12346778 Malignant neoplasm progression
123467782 12346778 Palmar-plantar erythrodysaesthesia syndrome

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
123467782 12346778 1 201406 0
123467782 12346778 2 201312 0
123467782 12346778 3 201403 201406 0