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
126414972 12641497 2 F 20160811 20160810 20160817 EXP BE-ELI_LILLY_AND_COMPANY-BE201608003140 ELI LILLY AND CO 0.00 M Y 0.00000 20160817 CN BE BE

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
126414972 12641497 1 PS ALIMTA PEMETREXED DISODIUM 1 Unknown 500 MG/M2, CYCLICAL U 21462 500 MG/M**2 INJECTION
126414972 12641497 2 C CISPLATIN. CISPLATIN 1 Unknown UNK, UNKNOWN U U 0
126414972 12641497 3 C COVERAM AMLODIPINEPERINDOPRIL 1 Unknown UNK, UNKNOWN 0
126414972 12641497 4 C ASAFLOW ASPIRIN 1 Unknown UNK, UNKNOWN 0
126414972 12641497 5 C FOLAVIT 2 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126414972 12641497 1 Non-small cell lung cancer stage IV
126414972 12641497 2 Non-small cell lung cancer stage IV
126414972 12641497 3 Hypertension
126414972 12641497 4 Hypertension
126414972 12641497 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126414972 12641497 DE
126414972 12641497 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126414972 12641497 Bronchial fistula
126414972 12641497 Decreased appetite
126414972 12641497 Haemorrhagic tumour necrosis
126414972 12641497 Weight decreased

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

no results found

Therapies reported

no results found