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
125795942 12579594 2 F 20160627 20160914 20160721 20160920 EXP FR-PFIZER INC-2016349252 PFIZER 16.00 YR M Y 0.00000 20160920 OT FR FR

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
125795942 12579594 1 PS Tazocilline PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 Intravenous (not otherwise specified) 4 G, 4X/DAY 112 G Y 50750 4 G INJECTION QID
125795942 12579594 2 SS Tazocilline PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 UNK 112 G Y 50750 INJECTION
125795942 12579594 3 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 800 MG, 3X/WEEK Y 0 800 MG
125795942 12579594 4 SS ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Oral 25 MG, 1X/DAY 375 MG Y 0 25 MG FILM-COATED TABLET QD
125795942 12579594 5 SS ORACILLIN /00001802/ PENICILLIN V POTASSIUM 1 Oral 1 MILLION IU, 2X/DAY Y 0 1 MIU TABLET BID
125795942 12579594 6 C SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, ONCE EVERY 2 WEEKS 0 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125795942 12579594 1 Bacterial sepsis
125795942 12579594 3 Prophylaxis
125795942 12579594 4 Sleep disorder
125795942 12579594 5 Prophylaxis
125795942 12579594 6 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
125795942 12579594 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125795942 12579594 Hypotension
125795942 12579594 Inflammation
125795942 12579594 Photosensitivity reaction
125795942 12579594 Pyrexia
125795942 12579594 Rash erythematous

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
125795942 12579594 1 20160618 20160624 0
125795942 12579594 2 20160627 20160629 0
125795942 12579594 3 20160613 20160629 0
125795942 12579594 4 20160613 20160627 0
125795942 12579594 5 201602 20160628 0
125795942 12579594 6 20160215 20160620 0