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
119266347 11926634 7 F 2015 20160915 20160119 20160919 EXP PHHY2015CA106368 NOVARTIS 55.80 YR F Y 0.00000 20160919 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
119266347 11926634 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) U 21008 30 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119266347 11926634 1 Neuroendocrine tumour

Outcome of event

Event ID CASEID OUTC COD
119266347 11926634 DE
119266347 11926634 OT
119266347 11926634 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119266347 11926634 Abdominal distension
119266347 11926634 Asthenia
119266347 11926634 Blood pressure increased
119266347 11926634 Blood pressure systolic increased
119266347 11926634 Death
119266347 11926634 Dehydration
119266347 11926634 Diarrhoea
119266347 11926634 Fatigue
119266347 11926634 Flushing
119266347 11926634 Heart rate decreased
119266347 11926634 Hot flush
119266347 11926634 Hyperhidrosis
119266347 11926634 Hypocalcaemia
119266347 11926634 Hyponatraemia
119266347 11926634 Intestinal obstruction
119266347 11926634 Local swelling
119266347 11926634 Lung disorder
119266347 11926634 Muscle atrophy
119266347 11926634 Nausea
119266347 11926634 Peripheral swelling
119266347 11926634 Pruritus
119266347 11926634 Rash generalised
119266347 11926634 Vomiting
119266347 11926634 Weight decreased

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
119266347 11926634 1 20150808 0