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
90613031 9061303 1 I 20120201 0 20130208 20130208 DIR 66.09 YR M N 95.10000 KG 20120205 RN 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
90613031 9061303 1 PS ALIMTA 1 INTRAVENOUS N 21462 Q3W
90613031 9061303 2 SS AVASTIN 1 INTRAVENOUS N 0 Q3W
90613031 9061303 3 SS CARBOPLATIN 1 INTRAVENOUS N 0 Q3W

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90613031 9061303 1 Non-small cell lung cancer
90613031 9061303 2 Non-small cell lung cancer
90613031 9061303 3 Non-small cell lung cancer

Outcome of event

Event ID CASEID OUTC COD
90613031 9061303 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
90613031 9061303 Deep vein thrombosis
90613031 9061303 Pulmonary embolism
90613031 9061303 Varicose vein

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

Event ID CASEID RPSR COD
90613031 9061303 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
90613031 9061303 1 20121112 20120114 0
90613031 9061303 2 20121112 20120114 0
90613031 9061303 3 20121112 20120114 0