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
123326493 12332649 3 F 2015 20160610 20160504 20160708 PER US-PFIZER INC-2016242465 PFIZER 73.00 YR F Y 0.00000 20160708 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
123326493 12332649 1 PS ACCUPRIL QUINAPRIL HYDROCHLORIDE 1 20 MG, UNK U 19885 20 MG FILM-COATED TABLET
123326493 12332649 2 SS ACCUPRIL QUINAPRIL HYDROCHLORIDE 1 40 MG, 1X/DAY U 19885 40 MG FILM-COATED TABLET QD
123326493 12332649 3 SS ACCUPRIL QUINAPRIL HYDROCHLORIDE 1 20 MG, 2X/DAY (20MG IN THE MORNING AND 20MG IN THE EVENING) U 19885 20 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123326493 12332649 1 Blood pressure management

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123326493 12332649 Blood pressure decreased
123326493 12332649 Drug ineffective
123326493 12332649 Feeling abnormal
123326493 12332649 Muscular weakness
123326493 12332649 Renal disorder

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
123326493 12332649 2 2015 0
123326493 12332649 3 2015 0