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
97730864 9773086 4 F 20080319 20160824 20131219 20160829 EXP US-PFIZER INC-2013363703 PFIZER 60.00 YR F Y 0.00000 20160829 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
97730864 9773086 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral UNK, AS DIRECTED U 20702 FILM-COATED TABLET
97730864 9773086 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG, DAILY U 20702 10 MG FILM-COATED TABLET
97730864 9773086 3 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG, DAILY U 20702 10 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97730864 9773086 1 Low density lipoprotein increased
97730864 9773086 2 Cardiovascular event prophylaxis
97730864 9773086 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
97730864 9773086 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97730864 9773086 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
97730864 9773086 1 2004 20050907 0
97730864 9773086 2 20050907 20070817 0
97730864 9773086 3 20070817 20080610 0