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
118481322 11848132 2 F 20160919 20151217 20160922 PER US-PFIZER INC-2015417317 PFIZER 0.00 F Y 0.00000 20160922 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
118481322 11848132 1 PS ERYTHROMYCIN. ERYTHROMYCIN 1 UNK U 50609
118481322 11848132 2 SS LIDOCAINE HCL LIDOCAINE HYDROCHLORIDE 1 UNK U 17549
118481322 11848132 3 SS MOTRIN IBUPROFEN 1 UNK U 18989
118481322 11848132 4 SS NORVASC AMLODIPINE BESYLATE 1 UNK U 19787
118481322 11848132 5 SS CORTISONE ACETATE. CORTISONE ACETATE 1 UNK U 8126
118481322 11848132 6 SS IBUPROFEN. IBUPROFEN 1 UNK U 18989
118481322 11848132 7 SS TETRACYCLINE HCL TETRACYCLINE HYDROCHLORIDE 1 UNK U 60347
118481322 11848132 8 SS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 UNK U 50670
118481322 11848132 9 SS POTASSIUM POTASSIUM 1 UNK U 0
118481322 11848132 10 SS ASPIRIN. ASPIRIN 1 UNK U 0
118481322 11848132 11 SS IODINE. IODINE 1 UNK U 0
118481322 11848132 12 SS LEVAQUIN LEVOFLOXACIN 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118481322 11848132 Drug hypersensitivity

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

no results found

Therapies reported

no results found