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
125004024 12500402 4 F 20160712 20160627 20160712 EXP US-PFIZER INC-2016273540 PFIZER 0.00 F Y 0.00000 20160712 OT 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
125004024 12500402 1 PS NEURONTIN GABAPENTIN 1 UNK 20235
125004024 12500402 2 C LYRICA PREGABALIN 1 UNK 0
125004024 12500402 3 C CELEBREX CELECOXIB 1 UNK 0
125004024 12500402 4 C PROCARDIA XL NIFEDIPINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125004024 12500402 1 Diabetic neuropathy

Outcome of event

Event ID CASEID OUTC COD
125004024 12500402 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125004024 12500402 Condition aggravated
125004024 12500402 Drug ineffective for unapproved indication
125004024 12500402 Periarthritis

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

no results found

Therapies reported

no results found