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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6251648 7037804 I 6251648-3 20090410 20090618 20090630 EXP US-PFIZER INC-2009230498 PFIZERINC 54 M Y 83.914 KG 20090630 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6251648 1011816532 PS LIPITOR 1 ORAL 40 MG, 1X/DAY UNKNOWN 020702
6251648 1011816533 SS LOPRESSOR 1 100 MG, UNK
6251648 1011816534 C VASOTEC 1 5 MG, 2X/DAY
6251648 1011816535 C PLAVIX 1 75 MG, UNK
6251648 1011816536 C ACETYLSALICYLIC ACID 2 325 MG, UNK
6251648 1011816537 C FISH OIL 2 UNK
6251648 1011816538 C ANTIDIARRHOEAL MICROORGANISMS 2 UNK
6251648 1011816539 C COENZYME Q10 1 200 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6251648 1011816532 MYOCARDIAL INFARCTION

Outcome of event

Event ID OUTC COD
6251648 HO
6251648 OT

Reactions reported

Event ID PT
6251648 CARDIAC DISORDER
6251648 HEART RATE DECREASED
6251648 HIGH DENSITY LIPOPROTEIN DECREASED
6251648 STENT-GRAFT MALFUNCTION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6251648 1011816532 20090330