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
126065641 12606564 1 I 20160725 0 20160728 20160728 DIR 56.00 YR F N 220.00000 LBS 20160727 N 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
126065641 12606564 1 PS RECLAST ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 INJECTION ONE TIME INTIO A VEIN N D 0 1 DF SUSPENSION FOR INJECTION 1X
126065641 12606564 2 C PRAVASTATIN. PRAVASTATIN 1 0
126065641 12606564 3 C DEXILANT DEXLANSOPRAZOLE 1 0
126065641 12606564 4 C CYCLOBENZAPRINE CYCLOBENZAPRINE 1 0
126065641 12606564 5 C LOSARTAN. LOSARTAN 1 0
126065641 12606564 6 C BUPROPION XL BUPROPION 1 0
126065641 12606564 7 C POTASSIUM POTASSIUM 1 0
126065641 12606564 8 C HYDROCLORATHIDE 2 0
126065641 12606564 9 C ACTRAM 2 0
126065641 12606564 10 C PREMARIN ESTROGENS, CONJUGATED 1 0
126065641 12606564 11 C MULTIVITAMIN VITAMINS 1 0
126065641 12606564 12 C BIOTENE NOS CETYLPYRIDINIUM CHLORIDE OR SODIUM FLUORIDE OR SODIUM MONOFLUOROPHOSPHATE OR GLUCOSE OXIDASELACTOFERRINLACTOPEROXIDASE BOVINELYSOZYME 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126065641 12606564 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
126065641 12606564 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126065641 12606564 Abasia
126065641 12606564 Blood pressure increased
126065641 12606564 Movement disorder
126065641 12606564 Pain
126065641 12606564 Therapy non-responder
126065641 12606564 Vomiting

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
126065641 12606564 1 20160725 20160725 0