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
81879102 8187910 2 F 20110807 20160823 20111018 20160915 EXP US-ROCHE-1005017 ROCHE 68.00 YR M Y 80.50000 KG 20160915 MD 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
81879102 8187910 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE: 03/AUG/2011 125085 10 MG/KG SOLUTION FOR INFUSION
81879102 8187910 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) LAST DOSE: 03/AUG/2011, ?DOSE DELAYED BY 7 DAYS ON 10/AUG/2011 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
81879102 8187910 1 Hepatocellular carcinoma
81879102 8187910 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
81879102 8187910 DE
81879102 8187910 OT
81879102 8187910 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
81879102 8187910 Colitis
81879102 8187910 Diarrhoea
81879102 8187910 Dyspnoea
81879102 8187910 Embolism
81879102 8187910 Muscular weakness
81879102 8187910 Pneumonitis
81879102 8187910 Tumour flare

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
81879102 8187910 1 20110621 0
81879102 8187910 2 20110621 0