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
125798661 12579866 1 I 20130513 20130514 20160721 20160721 EXP PHHO2013US006503 NOVARTIS 53.24 YR M Y 81.50000 KG 20160721 OT US 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
125798661 12579866 1 SS ETOPOSIDE. ETOPOSIDE 1 Unknown UNK U U 0
125798661 12579866 2 SS CISPLATIN. CISPLATIN 1 Unknown UNK U U 0
125798661 12579866 3 PS ODOMZO SONIDEGIB 1 Oral 400 MG, UNK U 205266 400 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125798661 12579866 1 Small cell lung cancer extensive stage
125798661 12579866 2 Small cell lung cancer extensive stage
125798661 12579866 3 Small cell lung cancer extensive stage

Outcome of event

Event ID CASEID OUTC COD
125798661 12579866 DE
125798661 12579866 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125798661 12579866 Bradycardia
125798661 12579866 Haemodynamic instability
125798661 12579866 Hypotension
125798661 12579866 Myocardial infarction
125798661 12579866 Nausea
125798661 12579866 Vomiting

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
125798661 12579866 1 20130417 0
125798661 12579866 2 20130417 0
125798661 12579866 3 20130417 20130513 0