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
124761572 12476157 2 F 20160510 20160712 20160617 20160722 EXP FR-ELI_LILLY_AND_COMPANY-FR201606003785 ELI LILLY AND CO 59.35 YR F Y 0.00000 20160721 CN 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
124761572 12476157 1 PS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1640 MG, CYCLICAL N U 20509 1640 MG INJECTION
124761572 12476157 2 SS CAELYX DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) 20 MG/KG, 2/M N U 0 20 MG/KG
124761572 12476157 3 SS CAELYX DOXORUBICIN HYDROCHLORIDE 1 Unknown 33 MG, UNKNOWN N U 0 33 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124761572 12476157 1 Lymphoma
124761572 12476157 2 Lymphoma

Outcome of event

Event ID CASEID OUTC COD
124761572 12476157 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
124761572 12476157 Drug ineffective
124761572 12476157 Neuropathy peripheral

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
124761572 12476157 1 20160226 20160408 0
124761572 12476157 2 20160422 20160506 0
124761572 12476157 3 20160524 20160617 0