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
124668722 12466872 2 F 20160718 20160615 20160802 EXP DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-118518 RANBAXY 51.00 YR M Y 83.00000 KG 20160802 CN 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
124668722 12466872 1 SS SIMVASTATIN. SIMVASTATIN 1 Oral UNK U Y 0
124668722 12466872 2 SS Atorvastatin ATORVASTATIN 1 Unknown UNK U U 0
124668722 12466872 3 PS LOVASTATIN. LOVASTATIN 1 Unknown UNK U U 77520
124668722 12466872 4 SS FLUVASTATIN FLUVASTATIN SODIUM 1 Unknown UNK U U 0
124668722 12466872 5 SS Fermentierter roter Reis RED YEAST 1 Oral 600 MG, DAILY Y Y 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124668722 12466872 1 Hyperlipidaemia
124668722 12466872 2 Hyperlipidaemia
124668722 12466872 3 Hyperlipidaemia
124668722 12466872 4 Product used for unknown indication
124668722 12466872 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124668722 12466872 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124668722 12466872 Arthralgia Arthralgia
124668722 12466872 Myopathy Myopathy

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
124668722 12466872 1 2007 2015 0
124668722 12466872 2 2007 2015 0
124668722 12466872 3 2007 2015 0
124668722 12466872 5 2015 0