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
125609341 12560934 1 I 20160608 20160708 20160715 20160715 EXP FR-ELI_LILLY_AND_COMPANY-FR201607002760 ELI LILLY AND CO 69.42 YR M Y 0.00000 20160715 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
125609341 12560934 1 PS ALIMTA PEMETREXED DISODIUM 1 Intravenous (not otherwise specified) 500 MG, UNKNOWN Y U 21462 500 MG INJECTION
125609341 12560934 2 SS CARBOPLATIN HOSPIRA CARBOPLATIN 1 Intravenous (not otherwise specified) UNK, UNKNOWN U 0
125609341 12560934 3 C ASPIRINA ASPIRIN 1 Y 0
125609341 12560934 4 C ATORVASTATIN ATORVASTATIN 1 Y 0
125609341 12560934 5 C XGEVA DENOSUMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125609341 12560934 1 Lung adenocarcinoma
125609341 12560934 2 Lung adenocarcinoma
125609341 12560934 3 Product used for unknown indication
125609341 12560934 4 Product used for unknown indication
125609341 12560934 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125609341 12560934 OT
125609341 12560934 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125609341 12560934 Decreased appetite
125609341 12560934 General physical health deterioration
125609341 12560934 Hepatocellular injury
125609341 12560934 Malnutrition
125609341 12560934 Off label use
125609341 12560934 Pericardial effusion

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
125609341 12560934 1 20160601 20160601 0
125609341 12560934 2 20160601 0