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
127899071 12789907 1 I 20160510 20160928 20160928 EXP US-KOWA-16US000870 KOWA PHARM 0.00 Y 0.00000 20160928 CN US US

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
127899071 12789907 1 PS LIVALO PITAVASTATIN CALCIUM 1 4 MG, UNK N 22363 4 MG TABLET QD
127899071 12789907 2 SS LIVALO PITAVASTATIN CALCIUM 1 2 MG, QD N 22363 2 MG TABLET QD
127899071 12789907 3 SS ZETIA EZETIMIBE 1 UNK N 0
127899071 12789907 4 SS ZETIA EZETIMIBE 1 N 0
127899071 12789907 5 C PRALUENT ALIROCUMAB 1 Subcutaneous 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127899071 12789907 1 Blood cholesterol increased
127899071 12789907 2 Blood triglycerides increased
127899071 12789907 3 Blood cholesterol increased
127899071 12789907 4 Blood triglycerides increased
127899071 12789907 5 Blood cholesterol

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127899071 12789907 Arthralgia
127899071 12789907 Musculoskeletal pain

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
127899071 12789907 1 2015 0
127899071 12789907 2 201604 0
127899071 12789907 3 2015 2015 0