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
114047372 11404737 2 F 20160804 20150821 20160815 PER US-BAYER-2015-399780 BAYER 0.00 F Y 0.00000 20160815 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
114047372 11404737 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
114047372 11404737 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
114047372 11404737 3 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
114047372 11404737 4 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
114047372 11404737 5 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 250 MG, UNK 0 250 MG
114047372 11404737 6 C MACROBID NITROFURANTOINNITROFURANTOIN MONOHYDRATE 1 UNK 0
114047372 11404737 7 C LYRICA PREGABALIN 1 UNK 0
114047372 11404737 8 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK 0
114047372 11404737 9 C MELOXICAM. MELOXICAM 1 UNK 0
114047372 11404737 10 C NAPROXEN. NAPROXEN 1 UNK 0
114047372 11404737 11 C HYDROCODONE W/ACETAMINOPHEN ACETAMINOPHENHYDROCODONE BITARTRATE 1 UNK 0
114047372 11404737 12 C GABAPENTIN. GABAPENTIN 1 UNK 0
114047372 11404737 13 C AMOXICILLIN. AMOXICILLIN 1 UNK 0
114047372 11404737 14 C AMOXICILLIN. AMOXICILLIN 1 UNK 0
114047372 11404737 15 C AMOXICILLIN. AMOXICILLIN 1 UNK 0
114047372 11404737 16 C CELEBREX CELECOXIB 1 UNK 0
114047372 11404737 17 C NORTRIPTYLINE NORTRIPTYLINE 1 UNK 0
114047372 11404737 18 C HYDROMORPHONE HYDROMORPHONE 1 UNK 0
114047372 11404737 19 C ZONISAMIDE. ZONISAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114047372 11404737 1 Sinusitis
114047372 11404737 2 Sinusitis
114047372 11404737 3 Sinusitis
114047372 11404737 4 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
114047372 11404737 OT
114047372 11404737 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114047372 11404737 Anhedonia
114047372 11404737 Anxiety
114047372 11404737 Burning sensation
114047372 11404737 Depression
114047372 11404737 Emotional distress
114047372 11404737 Fear
114047372 11404737 Injury
114047372 11404737 Neuropathy peripheral
114047372 11404737 Pain
114047372 11404737 Pain in extremity
114047372 11404737 Quality of life 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
114047372 11404737 1 20011005 20011009 0
114047372 11404737 2 20031030 20031105 0
114047372 11404737 3 20070104 20070110 0
114047372 11404737 4 20071220 20071226 0
114047372 11404737 5 20060621 20060627 0
114047372 11404737 6 20071211 0
114047372 11404737 7 2011 0
114047372 11404737 8 2011 0
114047372 11404737 9 20100609 0
114047372 11404737 10 20100616 0
114047372 11404737 11 2011 0
114047372 11404737 12 2011 0
114047372 11404737 13 2009 0
114047372 11404737 14 2012 0
114047372 11404737 15 2013 0
114047372 11404737 16 2014 0
114047372 11404737 17 2014 0
114047372 11404737 18 2011 0