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
124020252 12402025 2 F 201002 20160620 20160525 20160712 PER US-PFIZER INC-2016272127 PFIZER 68.00 YR M Y 94.00000 KG 20160712 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
124020252 12402025 1 PS VIAGRA SILDENAFIL CITRATE 1 50 MG, AS NEEDED 20895 50 MG FILM-COATED TABLET
124020252 12402025 2 SS VIAGRA SILDENAFIL CITRATE 1 100 MG, UNK 20895 100 MG FILM-COATED TABLET
124020252 12402025 3 SS VIAGRA SILDENAFIL CITRATE 1 Oral UNK (50MG -100 MG AS DIRECTED) 20895 FILM-COATED TABLET
124020252 12402025 4 C ALLOPURINOL. ALLOPURINOL 1 40 MG, 1X/DAY 0 40 MG QD
124020252 12402025 5 C BABY ASPIRIN ASPIRIN 1 81 MG, 1X/DAY 0 81 MG QD
124020252 12402025 6 C LIPITOR ATORVASTATIN CALCIUM 1 UNK UNK, DAILY 0
124020252 12402025 7 C LIPITOR ATORVASTATIN CALCIUM 1 10 MG, ALTERNATE DAY 0 10 MG QOD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124020252 12402025 1 Erectile dysfunction
124020252 12402025 4 Gout

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124020252 12402025 Drug effect incomplete
124020252 12402025 Expired product administered

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
124020252 12402025 3 20150722 0