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
125739061 12573906 1 I 20160719 20160720 20160720 PER US-ELI_LILLY_AND_COMPANY-US201607007205 ELI LILLY AND CO 0.00 F Y 0.00000 20160720 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
125739061 12573906 1 PS ALIMTA PEMETREXED DISODIUM 1 Unknown UNK, CYCLICAL 21462 INJECTION
125739061 12573906 2 C CARBOPLATIN. CARBOPLATIN 1 Unknown UNK, UNKNOWN 0
125739061 12573906 3 C FOLIC ACID. FOLIC ACID 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125739061 12573906 1 Lung neoplasm malignant
125739061 12573906 2 Lung neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
125739061 12573906 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125739061 12573906 Fatigue
125739061 12573906 Heart rate increased
125739061 12573906 Off label use

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

no results found

Therapies reported

no results found