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
110456949 11045694 9 F 2014 20160630 20150417 20160802 EXP PHHY2014CA025066 NOVARTIS 61.88 YR F Y 0.00000 20160802 OT CA CA

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
110456949 11045694 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (ONCE A MONTH) U 21008 30 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110456949 11045694 1 Neuroendocrine tumour

Outcome of event

Event ID CASEID OUTC COD
110456949 11045694 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110456949 11045694 Abdominal discomfort
110456949 11045694 Abdominal distension
110456949 11045694 Abdominal pain
110456949 11045694 Abdominal pain upper
110456949 11045694 Anal incontinence
110456949 11045694 Blood pressure increased
110456949 11045694 Chest pain
110456949 11045694 Circadian rhythm sleep disorder
110456949 11045694 Crying
110456949 11045694 Depressed mood
110456949 11045694 Diarrhoea
110456949 11045694 Dyspepsia
110456949 11045694 Emotional disorder
110456949 11045694 Fatigue
110456949 11045694 Heart rate decreased
110456949 11045694 Helicobacter infection
110456949 11045694 Hepatic lesion
110456949 11045694 Injection site haemorrhage
110456949 11045694 Injection site mass
110456949 11045694 Injection site pain
110456949 11045694 Insomnia
110456949 11045694 Malaise
110456949 11045694 Mood swings
110456949 11045694 Nausea
110456949 11045694 Tearfulness
110456949 11045694 Vomiting

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
110456949 11045694 1 20140106 0