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
125646181 12564618 1 I 20160704 20160718 20160718 EXP SE-AUROBINDO-AUR-APL-2016-09318 AUROBINDO 50.00 YR F Y 0.00000 20160718 CN SE SE

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
125646181 12564618 1 PS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Oral U U 77206 FILM-COATED TABLET
125646181 12564618 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Unknown U U 0
125646181 12564618 3 SS MIRTAZAPINE. MIRTAZAPINE 1 Oral U U 0
125646181 12564618 4 SS Pramipexole Tablet PRAMIPEXOLE 1 Unknown .35 MG, UNK U U 0 .35 MG TABLET
125646181 12564618 5 SS DEVITRE CHOLECALCIFEROL 1 Unknown U U 0
125646181 12564618 6 SS ORALOVITE ASCORBIC ACIDNIACINAMIDEPYRIDOXINERIBOFLAVINTHIAMINE 1 Oral UNK U U 0 FILM-COATED TABLET
125646181 12564618 7 SS BETOLVIDON CYANOCOBALAMIN 1 Unknown 1 MG, UNK U U 0 1 MG TABLET
125646181 12564618 8 SS FOLACIN /00024201/ FOLIC ACID 1 Unknown U U 0 TABLET
125646181 12564618 9 SS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown 25 MG, UNK U U 0 25 MG TABLET
125646181 12564618 10 SS LASIX FUROSEMIDE 1 Unknown U U 0
125646181 12564618 11 SS DUODOPA CARBIDOPALEVODOPA 1 Unknown U U 0
125646181 12564618 12 SS SINEMET CARBIDOPALEVODOPA 1 Unknown U U 0
125646181 12564618 13 SS OPRYMEA PRAMIPEXOLE DIHYDROCHLORIDE 1 Unknown 0.26 MG, UNK U U 0 .26 MG
125646181 12564618 14 SS SELEGILINE SELEGILINE 1 Oral 10 MG, UNK U U 0 10 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125646181 12564618 1 Product used for unknown indication
125646181 12564618 2 Product used for unknown indication
125646181 12564618 3 Product used for unknown indication
125646181 12564618 4 Product used for unknown indication
125646181 12564618 5 Product used for unknown indication
125646181 12564618 6 Product used for unknown indication
125646181 12564618 7 Product used for unknown indication
125646181 12564618 8 Product used for unknown indication
125646181 12564618 9 Product used for unknown indication
125646181 12564618 10 Product used for unknown indication
125646181 12564618 11 Product used for unknown indication
125646181 12564618 12 Product used for unknown indication
125646181 12564618 13 Product used for unknown indication
125646181 12564618 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125646181 12564618 LT
125646181 12564618 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125646181 12564618 Hypomagnesaemia
125646181 12564618 Hyponatraemia
125646181 12564618 Neuroleptic malignant syndrome
125646181 12564618 Rhabdomyolysis
125646181 12564618 Toxicity to various agents

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

no results found

Therapies reported

no results found