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
98832448 9883244 8 F 20131029 20160901 20140209 20160902 EXP DE-ROCHE-1322711 ROCHE 51.00 YR F Y 37.00000 KG 20160902 OT DE DE

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
98832448 9883244 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) 125085 7.5 MG/KG
98832448 9883244 2 SS PEMETREXED PEMETREXED 1 Intravenous (not otherwise specified) U 0 700 MG
98832448 9883244 3 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) 0 105 MG
98832448 9883244 4 C CARBOPLATIN. CARBOPLATIN 1 Unknown 0 715 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98832448 9883244 1 Lung neoplasm malignant
98832448 9883244 2 Lung neoplasm malignant
98832448 9883244 3 Lung neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
98832448 9883244 LT
98832448 9883244 DE
98832448 9883244 HO
98832448 9883244 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98832448 9883244 Anaemia
98832448 9883244 Decreased appetite
98832448 9883244 Diarrhoea
98832448 9883244 Fatigue
98832448 9883244 Haematemesis
98832448 9883244 Platelet count decreased
98832448 9883244 Pyrexia
98832448 9883244 Shock haemorrhagic
98832448 9883244 Somnolence
98832448 9883244 White blood cell count decreased

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
98832448 9883244 1 20130918 0
98832448 9883244 2 20130918 20131105 0
98832448 9883244 3 20130918 20131009 0
98832448 9883244 4 20131105 0