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
127888211 12788821 1 I 20160915 20160928 20160928 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-124859 RANBAXY 73.00 YR F Y 0.00000 20160928 OT GB 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
127888211 12788821 1 PS CARBOPLATIN. CARBOPLATIN 1 Unknown UNK U 77926
127888211 12788821 2 SS Pemetrexed PEMETREXED 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127888211 12788821 1 Lung adenocarcinoma stage IV
127888211 12788821 2 Lung adenocarcinoma stage IV

Outcome of event

Event ID CASEID OUTC COD
127888211 12788821 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127888211 12788821 Asthenia
127888211 12788821 Nausea
127888211 12788821 Neutropenic sepsis
127888211 12788821 Vomiting

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

no results found

Therapies reported

no results found