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
127872711 12787271 1 I 2011 20160923 20160928 20160928 EXP GXKR2016DE004510 SANDOZ 0.00 Y 0.00000 20160928 OT 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
127872711 12787271 1 PS PRAVASTATIN. PRAVASTATIN 1 Oral 20 MG, ONCE DAILY Y 76397 20 MG QD
127872711 12787271 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG, UNK Y Y 0 40 MG
127872711 12787271 3 SS INEGY EZETIMIBESIMVASTATIN 1 Oral 1 DF, ONCE DAILY 1827 DF Y 0 1 DF QD
127872711 12787271 4 SS SORTIS ATORVASTATIN 1 Oral 20 MG, ONCE DAILY Y Y 0 20 MG QD
127872711 12787271 5 SS SORTIS ATORVASTATIN 1 Oral 20 MG, ONCE DAILY Y Y 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127872711 12787271 1 Product used for unknown indication
127872711 12787271 2 Product used for unknown indication
127872711 12787271 3 Product used for unknown indication
127872711 12787271 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127872711 12787271 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127872711 12787271 Blood creatine phosphokinase increased
127872711 12787271 Hypoaesthesia
127872711 12787271 Myalgia
127872711 12787271 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
127872711 12787271 1 20110728 20111110 0
127872711 12787271 2 2005 0
127872711 12787271 3 2006 2011 0
127872711 12787271 4 1999 0
127872711 12787271 5 2004 0