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
127288351 12728835 1 I 20160829 20160909 20160909 EXP JP-009507513-1609JPN001352 MERCK 0.00 Y 0.00000 20160909 MD JP JP

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
127288351 12728835 1 PS ZETIA EZETIMIBE 1 Oral DAILY DOSAGE UNKNOWN U 21445 TABLET
127288351 12728835 2 C PITAVASTATIN CALCIUM PITAVASTATIN CALCIUM 1 Oral FORMULATION: POR; DAILY DOSAGE UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127288351 12728835 1 Dyslipidaemia

Outcome of event

Event ID CASEID OUTC COD
127288351 12728835 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127288351 12728835 Alanine aminotransferase increased
127288351 12728835 Aspartate aminotransferase increased
127288351 12728835 Blood creatine phosphokinase increased
127288351 12728835 Blood creatinine increased
127288351 12728835 Gallbladder disorder
127288351 12728835 Gamma-glutamyltransferase increased
127288351 12728835 Myopathy
127288351 12728835 Neoplasm malignant
127288351 12728835 Rhabdomyolysis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found