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
116115433 11611543 3 F 2008 20160825 20151008 20160829 EXP US-PFIZER INC-2015335617 PFIZER 43.00 YR F Y 82.00000 KG 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
116115433 11611543 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG TO 40 MG , DAILY U 20702 FILM-COATED TABLET
116115433 11611543 2 SS LIPITOR ATORVASTATIN CALCIUM 1 U 20702 FILM-COATED TABLET
116115433 11611543 3 SS LIPITOR ATORVASTATIN CALCIUM 1 U 20702 FILM-COATED TABLET
116115433 11611543 4 SS LIPITOR ATORVASTATIN CALCIUM 1 U 20702 FILM-COATED TABLET
116115433 11611543 5 SS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Oral UNK U 20702 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116115433 11611543 1 Blood cholesterol increased
116115433 11611543 2 Blood triglycerides increased
116115433 11611543 3 Low density lipoprotein increased
116115433 11611543 4 Cardiovascular event prophylaxis
116115433 11611543 5 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
116115433 11611543 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116115433 11611543 Gestational diabetes
116115433 11611543 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
116115433 11611543 1 1997 0