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
124183313 12418331 3 F 20151220 20160830 20160531 20160908 EXP US-PFIZER INC-2016264068 PFIZER 71.00 YR M Y 84.00000 KG 20160908 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
124183313 12418331 1 PS LIPITOR ATORVASTATIN CALCIUM 1 80 MG, UNK U 20702 80 MG FILM-COATED TABLET
124183313 12418331 2 SS LIPITOR ATORVASTATIN CALCIUM 1 40 MG, 1 A DAY, AT NIGHT U 20702 40 MG FILM-COATED TABLET QD
124183313 12418331 3 C PROTONIX PANTOPRAZOLE SODIUM 1 UNK 0
124183313 12418331 4 C RANEXA RANOLAZINE 1 UNK 0
124183313 12418331 5 C METOPROLOL. METOPROLOL 1 UNK 0
124183313 12418331 6 C IMDUR ISOSORBIDE MONONITRATE 1 UNK 0
124183313 12418331 7 C LOPRESSOR METOPROLOL TARTRATE 1 UNK 0
124183313 12418331 8 C PROCARDIA NIFEDIPINE 1 UNK 0
124183313 12418331 9 C BABY ASPIRIN ASPIRIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124183313 12418331 1 Blood cholesterol abnormal
124183313 12418331 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
124183313 12418331 OT
124183313 12418331 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124183313 12418331 Drug dispensing error
124183313 12418331 Dysstasia
124183313 12418331 Malaise
124183313 12418331 Muscular weakness
124183313 12418331 Myalgia
124183313 12418331 Weight decreased

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
124183313 12418331 2 2010 0