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
125865601 12586560 1 I 20160603 20160628 20160725 20160725 PER PR-PFIZER INC-2016324045 PFIZER 57.00 YR M Y 61.00000 KG 20160725 CN PR PR

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
125865601 12586560 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, 1X/DAY 20702 20 MG FILM-COATED TABLET QD
125865601 12586560 2 SS LIPITOR ATORVASTATIN CALCIUM 1 20702 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125865601 12586560 1 Blood cholesterol increased
125865601 12586560 2 Blood triglycerides increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125865601 12586560 Alanine aminotransferase increased
125865601 12586560 Aspartate aminotransferase increased
125865601 12586560 Blood count abnormal
125865601 12586560 Bone pain
125865601 12586560 Diarrhoea
125865601 12586560 Headache
125865601 12586560 Nausea
125865601 12586560 Pyrexia

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
125865601 12586560 1 20160530 0