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
100062133 10006213 3 F 2012 20140620 20140313 20140630 EXP US-PFIZER INC-2014070219 PFIZER 58.00 YR F Y 76.00000 KG 20140630 N LW 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
100062133 10006213 1 PS Lipitor 1 ORAL 20 MG, DAILY D 20702 20 MG FILM-COATED TABLET
100062133 10006213 2 SS Lipitor 1 ORAL 20 MG, DAILY D 20702 20 MG FILM-COATED TABLET
100062133 10006213 3 SS ATORVASTATIN CALCIUM 1 20 MG, DAILY D 20702 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100062133 10006213 1 Low density lipoprotein increased
100062133 10006213 3 Blood cholesterol abnormal

Outcome of event

Event ID CASEID OUTC COD
100062133 10006213 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100062133 10006213 Type 2 diabetes mellitus

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
100062133 10006213 1 200705 200904 0
100062133 10006213 2 201203 201205 0
100062133 10006213 3 201203 201306 0