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
127117111 12711711 1 I 20160504 20160819 20160902 20160902 EXP GB-AUROBINDO-AUR-APL-2016-10838 AUROBINDO 40.00 YR M Y 83.00000 KG 20160902 MD GB GB

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
127117111 12711711 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, TWO TIMES A DAY 54958.332 MG U U 77859 500 MG BID
127117111 12711711 2 C ALZAIN 2 Unknown 1 DF, TWO TIMES A DAY 94 DF U 0 1 DF BID
127117111 12711711 3 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 1 DF, ONCE A DAY 6 DF U 0 1 DF QD
127117111 12711711 4 C DERMOL /01330701/ 2 Unknown 1 DF, ONCE A DAY, OR WASHING. 721 DF U 0 1 DF QD
127117111 12711711 5 C PREGABALIN. PREGABALIN 1 Unknown 1 DF, TWO TIMES A DAY 58 DF U 0 1 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127117111 12711711 1 Prostatitis
127117111 12711711 2 Product used for unknown indication
127117111 12711711 3 Product used for unknown indication
127117111 12711711 4 Product used for unknown indication
127117111 12711711 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127117111 12711711 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127117111 12711711 Abdominal pain
127117111 12711711 Arthralgia
127117111 12711711 Bradyphrenia
127117111 12711711 Constipation
127117111 12711711 Dermatitis contact
127117111 12711711 Dyspnoea
127117111 12711711 Fatigue
127117111 12711711 Feeling abnormal
127117111 12711711 Hair colour changes
127117111 12711711 Heart rate increased
127117111 12711711 Inguinal mass
127117111 12711711 Insomnia
127117111 12711711 Joint stiffness
127117111 12711711 Malaise
127117111 12711711 Muscle twitching
127117111 12711711 Nausea
127117111 12711711 Night sweats
127117111 12711711 Palpitations
127117111 12711711 Rash
127117111 12711711 Suicidal ideation
127117111 12711711 Vision blurred
127117111 12711711 Vitreous floaters

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
127117111 12711711 1 20160310 0
127117111 12711711 2 20160620 0
127117111 12711711 3 20160510 20160607 0
127117111 12711711 4 20140514 0
127117111 12711711 5 20160602 20160603 0