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
126495191 12649519 1 I 20160808 20160812 20160812 EXP US-TEVA-684183USA TEVA SHIRLEY D-AT, FROH DK. AGRANULOCYTOSIS IN A PEDIATRIC PATIENT TREATED WITH CEFTAROLINE. J-PEDIATRIC-INFECT-DIS-SOC 2016;5(2):E5-E8. 13.00 YR F Y 0.00000 20160812 MD 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
126495191 12649519 1 PS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 70048
126495191 12649519 2 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Intravenous (not otherwise specified) HIGH DOSE 70048
126495191 12649519 3 SS ceftaroline fosamil CEFTAROLINE FOSAMIL 1 Intravenous (not otherwise specified) Y 0 400 MG Q8H
126495191 12649519 4 C MINOCYCLINE MINOCYCLINEMINOCYCLINE HYDROCHLORIDE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126495191 12649519 1 Staphylococcal infection
126495191 12649519 2 Staphylococcal infection
126495191 12649519 3 Staphylococcal infection
126495191 12649519 4 Stenotrophomonas infection

Outcome of event

Event ID CASEID OUTC COD
126495191 12649519 HO
126495191 12649519 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126495191 12649519 Agranulocytosis
126495191 12649519 Febrile neutropenia

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

no results found

Therapies reported

no results found