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
127177651 12717765 1 I 20091123 20160826 20160906 20160906 EXP IT-MINISAL02-372346 IT-MYLANLABS-2016M1036775 MYLAN 0.00 Y 0.00000 20160906 MD IT IT

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
127177651 12717765 1 PS SIMVASTATIN. SIMVASTATIN 1 UNK Y U 90868
127177651 12717765 2 SS ATORVASTATIN ATORVASTATIN 1 UNK Y U 0
127177651 12717765 3 SS PRAVASTATIN. PRAVASTATIN 1 UNK Y U 0
127177651 12717765 4 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 UNK Y U 0
127177651 12717765 5 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 UNK 0
127177651 12717765 6 C OLMESARTAN MEDOXOMIL. OLMESARTAN MEDOXOMIL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127177651 12717765 1 Type IIa hyperlipidaemia
127177651 12717765 2 Type IIa hyperlipidaemia
127177651 12717765 3 Type IIa hyperlipidaemia
127177651 12717765 4 Type IIa hyperlipidaemia
127177651 12717765 5 Product used for unknown indication
127177651 12717765 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127177651 12717765 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127177651 12717765 Myopathy
127177651 12717765 Pain in extremity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found