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
125271883 12527188 3 F 20160530 20160802 20160705 20160803 EXP PHHY2016LB083359 NOVARTIS 70.00 YR F Y 0.00000 20160803 CN COUNTRY NOT SPECIFIED LB

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
125271883 12527188 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK S0142 21817 5 MG SOLUTION FOR INJECTION
125271883 12527188 2 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral 75 MG, UNK 0 75 MG
125271883 12527188 3 C NOOTROPIL PIRACETAM 1 Oral 800 OT, TID 0 TID
125271883 12527188 4 C LIPANTHYL FENOFIBRATE 1 Oral 200 OT, QD 0 QD
125271883 12527188 5 C CRESTOR ROSUVASTATIN CALCIUM 1 Oral 10 MG, QD 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125271883 12527188 1 Osteoporosis
125271883 12527188 2 Product used for unknown indication
125271883 12527188 3 Product used for unknown indication
125271883 12527188 4 Product used for unknown indication
125271883 12527188 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125271883 12527188 HO
125271883 12527188 DE
125271883 12527188 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125271883 12527188 Blood albumin decreased
125271883 12527188 Death
125271883 12527188 Diarrhoea
125271883 12527188 Dysphagia
125271883 12527188 Loss of consciousness
125271883 12527188 Organ failure
125271883 12527188 Vision blurred

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
125271883 12527188 1 20160502 0