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
126583423 12658342 3 F 2016 20160907 20160817 20160921 EXP GB-AUROBINDO-AUR-APL-2016-10283 AUROBINDO 47.00 YR F Y 58.00000 KG 20160921 CN GB GB

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
126583423 12658342 1 PS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Unknown 100 MG, UNK Y U 77206 100 MG
126583423 12658342 2 SS CETIRIZINE CETIRIZINE HYDROCHLORIDE 1 Oral 10 MG, UNK Y U CB13L51 0 10 MG
126583423 12658342 3 SS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Oral 150 MG, UNK Y U 2758097 0 150 MG
126583423 12658342 4 SS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Oral 100 MG Y U 2758097 0 100 MG
126583423 12658342 5 C LORATADINE. LORATADINE 1 Unknown U 0
126583423 12658342 6 C PARACETAMOL ACETAMINOPHEN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126583423 12658342 1 Depression
126583423 12658342 2 Multiple allergies
126583423 12658342 3 Depression
126583423 12658342 5 Product used for unknown indication
126583423 12658342 6 Headache

Outcome of event

Event ID CASEID OUTC COD
126583423 12658342 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126583423 12658342 Abdominal discomfort
126583423 12658342 Blood pressure systolic increased
126583423 12658342 Depression
126583423 12658342 Drug ineffective
126583423 12658342 Headache
126583423 12658342 Inhibitory drug interaction

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
126583423 12658342 1 20160601 0
126583423 12658342 2 20160713 20160722 0
126583423 12658342 4 20160601 0