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
125414641 12541464 1 I 20160626 20160708 20160708 EXP US-ELI_LILLY_AND_COMPANY-US201607002145 ELI LILLY AND CO 69.00 YR M Y 0.00000 20160708 MD 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
125414641 12541464 1 PS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN Y 20509

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125414641 12541464 1 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
125414641 12541464 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125414641 12541464 Anaemia
125414641 12541464 Blood creatinine increased
125414641 12541464 Blood lactate dehydrogenase abnormal
125414641 12541464 Platelet count decreased
125414641 12541464 Thrombotic microangiopathy

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found