The Safety Rates Drug Report

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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
127892861 12789286 1 I 2011 20160923 20160928 20160928 EXP DE-DRREDDYS-GER/GER/16/0083601 DR REDDYS 44.00 YR M Y 110.00000 KG 20160928 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
127892861 12789286 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral Y Y UNKNOWN 77752 40 MG
127892861 12789286 2 SS PRAVASTATIN. PRAVASTATIN 1 Oral Y U 0 20 MG QD
127892861 12789286 3 SS Inegy 10 mg/40 mg EZETIMIBESIMVASTATIN 1 Oral 1827 DF Y U 0 1 DF QD
127892861 12789286 4 SS SORTIS 20 MG ATORVASTATIN 1 Oral Y U 0 20 MG QD
127892861 12789286 5 SS SORTIS 20 MG ATORVASTATIN 1 Oral Y U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127892861 12789286 1 Product used for unknown indication
127892861 12789286 2 Product used for unknown indication
127892861 12789286 3 Product used for unknown indication
127892861 12789286 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127892861 12789286 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127892861 12789286 Blood creatine phosphokinase increased Blood creatine phosphokinase increased
127892861 12789286 Hypoaesthesia Hypoaesthesia
127892861 12789286 Myalgia Myalgia
127892861 12789286 Polyneuropathy Polyneuropathy

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
127892861 12789286 1 2005 0
127892861 12789286 2 20110728 20111110 0
127892861 12789286 3 2006 2011 0
127892861 12789286 4 1999 0
127892861 12789286 5 2004 0