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
124734722 12473472 2 F 2013 20160914 20160616 20160922 EXP DE-MYLANLABS-2016M1024116 MYLAN 0.00 Y 0.00000 20160922 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
124734722 12473472 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 10 MG, UNK Y U 90868 10 MG
124734722 12473472 2 SS ATORVASTATIN ATORVASTATIN 1 Oral 10 MG, UNK Y U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124734722 12473472 1 Hyperlipidaemia
124734722 12473472 2 Hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
124734722 12473472 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124734722 12473472 Myalgia
124734722 12473472 Nightmare

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
124734722 12473472 1 2013 0
124734722 12473472 2 201509 201511 0