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
100476233 10047623 3 F 200104 20141229 20140331 20141231 EXP US-PFIZER INC-2014090124 PFIZER 79.00 YR F Y 65.00000 KG 20141231 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
100476233 10047623 1 PS LIPITOR ATORVASTATIN CALCIUM 1 ORAL 10 MG, DAILY D 20702 10 MG FILM-COATED TABLET
100476233 10047623 2 SS LIPITOR ATORVASTATIN CALCIUM 1 D 20702 FILM-COATED TABLET
100476233 10047623 3 SS LIPITOR ATORVASTATIN CALCIUM 1 D 20702 FILM-COATED TABLET
100476233 10047623 4 SS LIPITOR ATORVASTATIN CALCIUM 1 D 20702 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100476233 10047623 1 Low density lipoprotein increased
100476233 10047623 2 Cardiovascular event prophylaxis
100476233 10047623 3 Blood cholesterol increased
100476233 10047623 4 Blood triglycerides increased

Outcome of event

Event ID CASEID OUTC COD
100476233 10047623 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100476233 10047623 Limb injury
100476233 10047623 Neuropathy peripheral
100476233 10047623 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
100476233 10047623 1 200006 0