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
125223261 12522326 1 I 201408 20160619 20160701 20160701 EXP AU-VALIDUS PHARMACEUTICALS LLC-AU-2016VAL002217 VALIDUS 0.00 Y 0.00000 20160701 MD AU AU

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
125223261 12522326 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 25 MG, BID U 17963 25 MG
125223261 12522326 2 C ASPIRIN /00002701/ ASPIRIN 1 UNK U 0
125223261 12522326 3 C IRBESARTAN. IRBESARTAN 1 UNK U 0
125223261 12522326 4 C LERCANIDIPINE LERCANIDIPINE 1 UNK U 0
125223261 12522326 5 C TIOTROPIUM TIOTROPIUM 1 UNK U 0
125223261 12522326 6 C SALBUTAMOL ALBUTEROL 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125223261 12522326 1 Product used for unknown indication
125223261 12522326 2 Product used for unknown indication
125223261 12522326 3 Product used for unknown indication
125223261 12522326 4 Product used for unknown indication
125223261 12522326 5 Product used for unknown indication
125223261 12522326 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125223261 12522326 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125223261 12522326 Asthenia
125223261 12522326 Atrial fibrillation
125223261 12522326 Blood pressure increased
125223261 12522326 Cardiac failure
125223261 12522326 Cardiac failure congestive
125223261 12522326 Crepitations
125223261 12522326 Decreased appetite
125223261 12522326 Depression
125223261 12522326 Dyspnoea
125223261 12522326 Fatigue
125223261 12522326 Grief reaction
125223261 12522326 Heart rate irregular
125223261 12522326 Hypotension
125223261 12522326 Oedema peripheral
125223261 12522326 Orthopnoea
125223261 12522326 Osteoporosis
125223261 12522326 Peripheral swelling

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

no results found

Therapies reported

no results found