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
127116931 12711693 1 I 20160822 20160902 20160902 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122835 RANBAXY 0.00 F Y 0.00000 20160902 OT GB GB

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
127116931 12711693 1 PS CARBOPLATIN. CARBOPLATIN 1 Unknown TWO CYCLES N U 77926
127116931 12711693 2 SS Pemetrexed PEMETREXED 1 Unknown THREE CYCLES U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127116931 12711693 1 Non-small cell lung cancer
127116931 12711693 2 Non-small cell lung cancer

Outcome of event

Event ID CASEID OUTC COD
127116931 12711693 OT
127116931 12711693 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127116931 12711693 Asthenia
127116931 12711693 Diarrhoea
127116931 12711693 Full blood count decreased

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

no results found

Therapies reported

no results found