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
127912871 12791287 1 I 20120501 20120526 20160929 20160929 EXP US-ROCHE-1073226 ROCHE 82.00 YR F Y 67.00000 KG 20160929 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
127912871 12791287 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MIN ON DAYS 1 AND 15 (10 MG/KG) Y 125085 670 MG
127912871 12791287 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1,8, 15, 22 0 75 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127912871 12791287 1 Malignant neoplasm of islets of Langerhans
127912871 12791287 2 Malignant neoplasm of islets of Langerhans

Outcome of event

Event ID CASEID OUTC COD
127912871 12791287 HO
127912871 12791287 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127912871 12791287 Anaemia
127912871 12791287 Cardiac failure

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
127912871 12791287 1 20120403 20120417 0
127912871 12791287 2 20120403 20120417 0