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
125749641 12574964 1 I 20160531 20160706 20160720 20160720 EXP CH-TEVA-675425ISR TEVA 47.00 YR M Y 90.00000 KG 20160720 MD CH CH

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
125749641 12574964 1 PS Irfen IBUPROFEN 1 Oral 1600 MILLIGRAM DAILY; USED DAILY FOR ABOUT 4 MONTHS, PREVIOUSLY HE HAD USED OTHER NSAIDS Y 71145 800 MG BID
125749641 12574964 2 SS COSENTYX SECUKINUMAB 1 Subcutaneous IN TOTAL, 2 DOSES WERE ADMINISTERED, ONE ON 31-MAY-2016 AND ONE ON 07-JUN-2016 U 0 150 MG /wk
125749641 12574964 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 20 MILLIGRAM DAILY; USED SINCE YEARS 0 20 MG QD
125749641 12574964 4 C PANTOZOL PANTOPRAZOLE SODIUM 1 Oral 40 MILLIGRAM DAILY; LONG-TERM THERAPY, WAS REPLACED WITH ESOMEPRAZOLE ON 15-JUN-2016 U 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125749641 12574964 1 Back pain
125749641 12574964 2 Spondylitis
125749641 12574964 3 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
125749641 12574964 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125749641 12574964 Off label use
125749641 12574964 Pancreatitis necrotising
125749641 12574964 Portal vein thrombosis
125749641 12574964 Splenic thrombosis

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
125749641 12574964 1 201602 20160614 0
125749641 12574964 2 20160531 20160607 0
125749641 12574964 4 20160614 0