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
122351712 12235171 2 F 20160111 20160829 20160404 20160901 EXP FR-ELI_LILLY_AND_COMPANY-FR201603007450 ELI LILLY AND CO 49.68 YR F Y 61.00000 KG 20160901 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
122351712 12235171 1 PS ALIMTA PEMETREXED DISODIUM 1 Unknown 830 MG, CYCLICAL Y U 21462 830 MG INJECTION
122351712 12235171 2 SS ALIMTA PEMETREXED DISODIUM 1 Unknown UNK UNK, CYCLICAL Y U 21462 INJECTION
122351712 12235171 3 SS CARBOPLATIN HOSPIRA CARBOPLATIN 1 Unknown UNK, CYCLICAL Y U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122351712 12235171 1 Lung adenocarcinoma stage I
122351712 12235171 3 Lung adenocarcinoma stage I

Outcome of event

Event ID CASEID OUTC COD
122351712 12235171 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122351712 12235171 Cholestasis
122351712 12235171 Condition aggravated
122351712 12235171 Hepatocellular injury
122351712 12235171 Off label use

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
122351712 12235171 1 20160111 0
122351712 12235171 2 20160201 20160209 0
122351712 12235171 3 20160201 20160209 0