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
127410471 12741047 1 I 20100621 20110607 20160914 20160914 EXP US-ROCHE-783254 ROCHE 79.97 YR M Y 76.70000 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
127410471 12741047 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) CYCLE 28 DAYS; OVER 30-90 MINUTES ON DAYS 1 AND 15; PATIENT WAS OFF STUDY SINCE 06 JULY 2010?LAST TR 125085 1536 MG
127410471 12741047 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) CYCLE 28 DAYS; ON DAYS 1, 8, 15, 22; PATIENT WAS OFF STUDY SINCE 06 JULY 2010.?LAST TREATMENT RECEIV 0 75 MG
127410471 12741047 3 SS MEGESTROL ACETATE. MEGESTROL ACETATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127410471 12741047 1 Pancreatic neoplasm
127410471 12741047 2 Pancreatic neoplasm
127410471 12741047 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127410471 12741047 LT
127410471 12741047 HO
127410471 12741047 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127410471 12741047 Dyspnoea
127410471 12741047 Fatigue
127410471 12741047 Hyperglycaemia
127410471 12741047 Left ventricular dysfunction
127410471 12741047 Muscular weakness
127410471 12741047 Oedema peripheral
127410471 12741047 Pleural effusion
127410471 12741047 Pulmonary 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
127410471 12741047 1 20100525 20100608 0