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
125402442 12540244 2 F 201002 20160715 20160708 20160725 EXP US-PFIZER INC-2016333914 PFIZER 70.00 YR F Y 65.00000 KG 20160725 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
125402442 12540244 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG, 1X/DAY U 20702 10 MG FILM-COATED TABLET QD
125402442 12540244 2 SS LIPITOR ATORVASTATIN CALCIUM 1 U 20702 FILM-COATED TABLET
125402442 12540244 3 SS LIPITOR ATORVASTATIN CALCIUM 1 U 20702 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125402442 12540244 1 Hypercholesterolaemia
125402442 12540244 2 Blood cholesterol increased
125402442 12540244 3 Hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
125402442 12540244 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125402442 12540244 Aortic arteriosclerosis
125402442 12540244 Aortic valve incompetence
125402442 12540244 Dermatitis
125402442 12540244 Myalgia
125402442 12540244 Neuropathy peripheral
125402442 12540244 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
125402442 12540244 1 200402 2013 0