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
127412081 12741208 1 I 20100303 20140607 20160914 20160914 EXP US-ROCHE-1415898 ROCHE 47.00 YR M Y 114.00000 KG 20160914 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
127412081 12741208 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MIN ON DAYS 1 AND 15?LAST DOSE ADMINISTERED ON 25/FEB/2010 125085 10 MG/KG SOLUTION FOR INFUSION
127412081 12741208 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1,8, 15, 22.?LAST DOSE ADMINISTERED ON 25/FEB/2010 U 0 25 MG
127412081 12741208 3 C OCTREOTIDE. OCTREOTIDE 1 Unknown 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127412081 12741208 1 Pancreatic neoplasm
127412081 12741208 2 Pancreatic neoplasm

Outcome of event

Event ID CASEID OUTC COD
127412081 12741208 OT
127412081 12741208 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127412081 12741208 Anaemia
127412081 12741208 Hyponatraemia
127412081 12741208 Lymphocyte count decreased
127412081 12741208 Oesophageal varices haemorrhage
127412081 12741208 Platelet count decreased
127412081 12741208 Stomatitis
127412081 12741208 Upper gastrointestinal haemorrhage

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
127412081 12741208 1 20100126 0
127412081 12741208 2 20100126 20140403 0
127412081 12741208 3 200708 0