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
123129194 12312919 4 F 20160831 20160428 20160908 EXP AU-SA-2016SA079952 AVENTIS 37.00 YR A M Y 86.00000 KG 20160908 MD AU AU

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
123129194 12312919 1 PS FABRAZYME AGALSIDASE BETA 1 Intravenous drip UNKNOWN 103979 .877 MG/KG POWDER FOR SOLUTION FOR INFUSION QOW
123129194 12312919 2 C ATORVASTATIN ATORVASTATIN 1 10 MG PM 0 10 MG
123129194 12312919 3 C MOVICOL POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE 1 DAILY +/- PM 0 QD
123129194 12312919 4 C PERINDOPRIL PERINDOPRIL 1 PM 0 2.5 MG
123129194 12312919 5 C COLOXYL DOCUSATE SODIUM 1 0
123129194 12312919 6 C LYRICA PREGABALIN 1 300 MG IN AM AND 275 MG IN PM 0
123129194 12312919 7 C MAGNESIUM MAGNESIUM 1 0 400 MG BID
123129194 12312919 8 C PALEXIA TAPENTADOL HYDROCHLORIDE 1 0 150 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123129194 12312919 1 Fabry's disease
123129194 12312919 6 Pain
123129194 12312919 8 Pain

Outcome of event

Event ID CASEID OUTC COD
123129194 12312919 DS
123129194 12312919 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123129194 12312919 Asthenia
123129194 12312919 Body temperature increased
123129194 12312919 Hypertension
123129194 12312919 Joint lock
123129194 12312919 Neuralgia
123129194 12312919 Oedema peripheral
123129194 12312919 Pain
123129194 12312919 Vertigo
123129194 12312919 Weight 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
123129194 12312919 1 20151221 0