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
107976327 10797632 7 F 2015 20160711 20150216 20160808 PER US-PFIZER INC-2015049814 PFIZER 74.00 YR M Y 100.00000 KG 20160808 MD 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
107976327 10797632 1 PS CADUET AMLODIPINE BESYLATEATORVASTATIN CALCIUM 1 [AMLODIPINE BESILATE 10 MG]/[ATORVASTATIN CALCIUM 80 MG], 1 PILL,ONCE DAILY IN THE MORNING WITH FOOD Y U 0712061 21540 1 DF FILM-COATED TABLET QD
107976327 10797632 2 SS CADUET AMLODIPINE BESYLATEATORVASTATIN CALCIUM 1 Y U 21540 FILM-COATED TABLET
107976327 10797632 3 C IBUPROFEN. IBUPROFEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107976327 10797632 1 Hypertension
107976327 10797632 2 Hypercholesterolaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
107976327 10797632 Blood pressure fluctuation
107976327 10797632 Dizziness

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
107976327 10797632 1 201501 0