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
118330613 11833061 3 F 20131007 20160711 20151214 20160720 EXP US-JNJFOC-20151208356 JANSSEN 85.75 YR E F Y 0.00000 20160720 CN 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
118330613 11833061 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
118330613 11833061 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
118330613 11833061 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 22406 20 MG TABLET
118330613 11833061 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y 0 UNSPECIFIED
118330613 11833061 5 C NIFEDIPINE. NIFEDIPINE 1 Unknown 0 60 MG UNKNOWN
118330613 11833061 6 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Unknown 0 100 MG UNSPECIFIED
118330613 11833061 7 C FERROUS SULFATE. FERROUS SULFATE 1 Unknown 0 325 MG UNSPECIFIED
118330613 11833061 8 C SEROQUEL QUETIAPINE FUMARATE 1 Unknown 0 100 MG UNSPECIFIED
118330613 11833061 9 C ISOSORBIDE DINITRATE. ISOSORBIDE DINITRATE 1 Unknown 0 60 MG UNSPECIFIED
118330613 11833061 10 C OXYCODONE OXYCODONE 1 Unknown 0 10 MG UNSPECIFIED
118330613 11833061 11 C SIMVASTATIN. SIMVASTATIN 1 Unknown 0 40 MG UNSPECIFIED
118330613 11833061 12 C MEGESTROL MEGESTROL 1 Unknown 0 40 MG UNSPECIFIED
118330613 11833061 13 C TEMAZEPAM. TEMAZEPAM 1 Unknown 0 15 MG UNSPECIFIED
118330613 11833061 14 C GABAPENTIN. GABAPENTIN 1 Unknown 0 100 MG UNSPECIFIED
118330613 11833061 15 C DIOVAN VALSARTAN 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118330613 11833061 1 Deep vein thrombosis
118330613 11833061 2 Cerebrovascular accident prophylaxis
118330613 11833061 3 Atrial fibrillation
118330613 11833061 4 Product used for unknown indication
118330613 11833061 5 Product used for unknown indication
118330613 11833061 6 Product used for unknown indication
118330613 11833061 7 Product used for unknown indication
118330613 11833061 8 Product used for unknown indication
118330613 11833061 9 Product used for unknown indication
118330613 11833061 10 Product used for unknown indication
118330613 11833061 11 Product used for unknown indication
118330613 11833061 12 Product used for unknown indication
118330613 11833061 13 Product used for unknown indication
118330613 11833061 14 Product used for unknown indication
118330613 11833061 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118330613 11833061 DE
118330613 11833061 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118330613 11833061 Acute kidney injury
118330613 11833061 Pneumonia
118330613 11833061 Subdural haematoma

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
118330613 11833061 1 20130708 20131007 0
118330613 11833061 2 20130708 20131007 0
118330613 11833061 3 20130708 20131007 0
118330613 11833061 7 2013 0
118330613 11833061 9 2013 0
118330613 11833061 11 2013 0
118330613 11833061 12 2013 0
118330613 11833061 15 2013 0