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
124082202 12408220 2 F 201506 20160715 20160526 20160720 EXP US-PFIZER INC-2016274081 PFIZER 53.00 YR F Y 93.00000 KG 20160720 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
124082202 12408220 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, DAILY 20702 20 MG FILM-COATED TABLET
124082202 12408220 2 SS LIPITOR ATORVASTATIN CALCIUM 1 20702 FILM-COATED TABLET
124082202 12408220 3 SS LIPITOR ATORVASTATIN CALCIUM 1 20702 FILM-COATED TABLET
124082202 12408220 4 SS LIPITOR ATORVASTATIN CALCIUM 1 20702 FILM-COATED TABLET
124082202 12408220 5 SS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Oral 20 MG, DAILY U 20702 20 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124082202 12408220 1 Low density lipoprotein increased
124082202 12408220 2 Cardiovascular event prophylaxis
124082202 12408220 3 Blood cholesterol increased
124082202 12408220 4 Blood cholesterol abnormal
124082202 12408220 5 Blood cholesterol abnormal

Outcome of event

Event ID CASEID OUTC COD
124082202 12408220 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124082202 12408220 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
124082202 12408220 1 201203 201206 0
124082202 12408220 5 201308 201508 0