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
126900191 12690019 1 I 201306 20160823 20160826 20160826 EXP US-ASTELLAS-2016US032910 ASTELLAS 64.41 YR F Y 0.00000 20160826 OT 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
126900191 12690019 1 PS Erlotinib ERLOTINIB 1 Unknown 21743 100 MG TABLET QD
126900191 12690019 2 SS Erlotinib ERLOTINIB 1 Oral 83093P1CW 21743 75 MG TABLET QD
126900191 12690019 3 SS Erlotinib ERLOTINIB 1 Unknown UNK, UNKNOWN FREQ. 21743 TABLET
126900191 12690019 4 SS Erlotinib ERLOTINIB 1 Unknown 21743 150 MG TABLET QD
126900191 12690019 5 SS MORPHINE MORPHINE 1 Unknown UNK, UNKNOWN FREQ. 0 FORMULATION UNKNOWN
126900191 12690019 6 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126900191 12690019 7 C GABAPENTIN. GABAPENTIN 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126900191 12690019 8 C SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126900191 12690019 9 C PREDNISONE. PREDNISONE 1 Unknown U 0 5 MG TABLET
126900191 12690019 10 C PRAVASTATIN. PRAVASTATIN 1 Unknown U 0 20 MG TABLET
126900191 12690019 11 C RANITIDINE HCL RANITIDINE HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126900191 12690019 12 C SERTRALINE HCL SERTRALINE HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126900191 12690019 13 C AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126900191 12690019 1 Non-small cell lung cancer
126900191 12690019 2 Lung neoplasm malignant
126900191 12690019 5 Cancer pain
126900191 12690019 6 Chronic obstructive pulmonary disease
126900191 12690019 7 Product used for unknown indication
126900191 12690019 8 Product used for unknown indication
126900191 12690019 9 Product used for unknown indication
126900191 12690019 10 Product used for unknown indication
126900191 12690019 11 Product used for unknown indication
126900191 12690019 12 Product used for unknown indication
126900191 12690019 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126900191 12690019 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126900191 12690019 Constipation
126900191 12690019 Death
126900191 12690019 Diarrhoea
126900191 12690019 Fatigue
126900191 12690019 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
126900191 12690019 2 20130505 0
126900191 12690019 3 201306 0
126900191 12690019 4 201507 0