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
118052462 11805246 2 F 20160706 20151206 20160708 EXP IT-MINISAL02-335652 IT-MYLANLABS-2015M1042204 MYLAN 0.00 Y 0.00000 20160708 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
118052462 11805246 1 PS LAMIVUDINE. LAMIVUDINE 1 U U 204002
118052462 11805246 2 SS DIBASE CHOLECALCIFEROL 1 U U 0
118052462 11805246 3 SS FOLINA /00024201/ FOLIC ACID 1 U U 0
118052462 11805246 4 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 U U 0
118052462 11805246 5 SS KALETRA LOPINAVIRRITONAVIR 1 U U 0
118052462 11805246 6 SS HARVONI LEDIPASVIRSOFOSBUVIR 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118052462 11805246 1 Product used for unknown indication
118052462 11805246 2 Product used for unknown indication
118052462 11805246 3 Product used for unknown indication
118052462 11805246 4 Product used for unknown indication
118052462 11805246 5 Product used for unknown indication
118052462 11805246 6 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
118052462 11805246 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118052462 11805246 Anaemia
118052462 11805246 Epilepsy

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

no results found

Therapies reported

no results found