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
125302232 12530223 2 F 201605 20160705 20160706 20160802 PER US-PFIZER INC-2016291428 PFIZER 65.00 YR M Y 94.00000 KG 20160802 CN 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
125302232 12530223 1 PS CADUET AMLODIPINE BESYLATEATORVASTATIN CALCIUM 1 Oral [AMLODIPINE BESILATE 10 MICROGRAM/ATORVASTATIN CALCIUM 10 MICROGRAM] ONE TABLET BY MOUTH ONCE A DAY 21540 FILM-COATED TABLET QD
125302232 12530223 2 SS CADUET AMLODIPINE BESYLATEATORVASTATIN CALCIUM 1 21540 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125302232 12530223 1 Hypertension
125302232 12530223 2 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125302232 12530223 Blood cholesterol increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found