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
123398353 12339835 3 F 201507 20160831 20160506 20160905 EXP DE-ROCHE-1741953 ROCHE 60.00 YR F Y 82.00000 KG 20160905 MD DE DE

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
123398353 12339835 1 PS RIBAVIRIN. RIBAVIRIN 1 Oral U 21511 1200 MG
123398353 12339835 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral U 21511 600 MG
123398353 12339835 3 SS SOFOSBUVIR SOFOSBUVIR 1 Oral U 0 400 MG QD
123398353 12339835 4 C FORAIR (GERMANY) 2 0
123398353 12339835 5 C ALVESCO CICLESONIDE 1 Unknown 0 160 UG
123398353 12339835 6 C NEBILET NEBIVOLOL 1 Unknown 0 5 MG
123398353 12339835 7 C PANTOZOL PANTOPRAZOLE SODIUM 1 Unknown AS REQUIRED 0
123398353 12339835 8 C LAFAMME DIENOGESTESTRADIOL VALERATE 1 Unknown 0 .5 MG
123398353 12339835 9 C BUDIAIR BUDESONIDE 1 Unknown 0 200 UG
123398353 12339835 10 C UNACID PD SULTAMICILLIN TOSYLATE 1 Unknown AS REQUIRED 0 375 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123398353 12339835 1 Chronic hepatitis C
123398353 12339835 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
123398353 12339835 OT
123398353 12339835 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123398353 12339835 Dizziness
123398353 12339835 Fall
123398353 12339835 Gait disturbance
123398353 12339835 Gastrooesophageal reflux disease
123398353 12339835 Haemoglobin decreased
123398353 12339835 Insomnia
123398353 12339835 Migraine with aura
123398353 12339835 Pneumonia
123398353 12339835 Syncope
123398353 12339835 Urinary tract infection

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
123398353 12339835 1 20150630 0
123398353 12339835 2 20150924 0
123398353 12339835 3 20150630 20150924 0