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
100160733 10016073 3 F 20050928 20140620 20140317 20140630 EXP US-PFIZER INC-2014073012 PFIZER 72.00 YR F Y 72.56000 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
100160733 10016073 1 PS Lipitor 1 ORAL 10 MG, DAILY D 20702 10 MG FILM-COATED TABLET
100160733 10016073 2 SS Lipitor 1 ORAL 20 MG, DAILY D 20702 20 MG FILM-COATED TABLET
100160733 10016073 3 SS ATORVASTATIN CALCIUM 1 ORAL 20 MG, DAILY D 20702 20 MG FILM-COATED TABLET
100160733 10016073 4 C DYAZIDE 1 1 DF, DAILY D 0 1 DF
100160733 10016073 5 C DYAZIDE 1 D 0
100160733 10016073 6 C CALCIUM 1 1200 MG, DAILY D 0 1200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100160733 10016073 1 Low density lipoprotein increased
100160733 10016073 2 Cardiovascular event prophylaxis
100160733 10016073 3 Hypercholesterolaemia
100160733 10016073 4 Blood pressure abnormal
100160733 10016073 5 Cardiac disorder
100160733 10016073 6 Vitamin supplementation

Outcome of event

Event ID CASEID OUTC COD
100160733 10016073 OT
100160733 10016073 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100160733 10016073 Renal failure
100160733 10016073 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
100160733 10016073 1 200003 200706 0
100160733 10016073 2 20100810 0
100160733 10016073 3 20100810 0
100160733 10016073 4 199901 0
100160733 10016073 6 200401 0