The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

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
125219471 12521947 1 I 20160624 20160701 20160701 EXP US-ELI_LILLY_AND_COMPANY-US201606010743 ELI LILLY AND CO 32.00 YR F Y 0.00000 20160701 CN GB 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
125219471 12521947 1 PS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 20509
125219471 12521947 2 SS PACLITAXEL. PACLITAXEL 1 Unknown UNK, UNKNOWN U 0
125219471 12521947 3 SS ADRIAMYCIN DOXORUBICIN HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0
125219471 12521947 4 SS IFOSFAMIDE. IFOSFAMIDE 1 Unknown UNK, UNKNOWN U 0
125219471 12521947 5 SS DOXORUBICIN DOXORUBICIN 1 Unknown UNK, UNKNOWN U 0
125219471 12521947 6 SS DOCETAXEL. DOCETAXEL 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125219471 12521947 1 Angiosarcoma
125219471 12521947 2 Angiosarcoma
125219471 12521947 3 Angiosarcoma
125219471 12521947 4 Angiosarcoma
125219471 12521947 5 Angiosarcoma
125219471 12521947 6 Angiosarcoma

Outcome of event

Event ID CASEID OUTC COD
125219471 12521947 OT
125219471 12521947 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125219471 12521947 Ascites
125219471 12521947 Bone marrow failure
125219471 12521947 Hepatic failure
125219471 12521947 Hepatocellular injury
125219471 12521947 Off label use

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found