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
124600373 12460037 3 F 20151201 20160706 20160613 20160713 PER US-PFIZER INC-2016272058 PFIZER 59.00 YR M Y 0.00000 20160713 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
124600373 12460037 1 PS LIPITOR ATORVASTATIN CALCIUM 1 20 MG, UNK Y RX7840927 20702 20 MG FILM-COATED TABLET
124600373 12460037 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, 1X/DAY (QHS) Y 20702 20 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124600373 12460037 1 Blood cholesterol increased
124600373 12460037 2 Hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
124600373 12460037 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124600373 12460037 Blood creatine phosphokinase increased
124600373 12460037 Depression
124600373 12460037 Myalgia
124600373 12460037 Myopathy
124600373 12460037 Pain
124600373 12460037 Rash

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
124600373 12460037 1 201501 201510 0
124600373 12460037 2 201512 0