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
111205182 11120518 2 F 20140825 20160823 20150518 20160904 EXP US-ROCHE-1577660 ROCHE 61.00 YR M Y 99.00000 KG 20160905 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
111205182 11120518 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE ADMINISTERED ON 04/AUG/2015 (SINGLE DOSE) 125085 15 MG/KG
111205182 11120518 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) ON DAY 1 OF EACH CYCLE BEGINNING ON CYCLE 5 125085 15 MG/KG
111205182 11120518 3 SS IPILIMUMAB IPILIMUMAB 1 Intravenous (not otherwise specified) 296 MG 0 3 MG/KG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111205182 11120518 1 Malignant melanoma
111205182 11120518 3 Malignant melanoma

Outcome of event

Event ID CASEID OUTC COD
111205182 11120518 OT
111205182 11120518 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
111205182 11120518 Alanine aminotransferase increased
111205182 11120518 Aspartate aminotransferase increased
111205182 11120518 Death
111205182 11120518 Lipase increased

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
111205182 11120518 1 20140804 0
111205182 11120518 2 20140825 0
111205182 11120518 3 20140804 0