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
127642371 12764237 1 I 201512 20160914 20160920 20160920 EXP US-PFIZER INC-2016434305 PFIZER 62.00 YR F Y 68.00000 KG 20160920 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
127642371 12764237 1 PS LIPITOR ATORVASTATIN CALCIUM 1 UNK U 20702 FILM-COATED TABLET
127642371 12764237 2 C LASIX FUROSEMIDE 1 Oral 80 MG, 2X/DAY 0 80 MG TABLET BID
127642371 12764237 3 C COREG CARVEDILOL 1 Oral 12.5 MG, 2X/DAY 0 12.5 MG TABLET BID
127642371 12764237 4 C COREG CARVEDILOL 1 0 TABLET
127642371 12764237 5 C ENTRESTO SACUBITRILVALSARTAN 1 Oral [SACUBITRIL 24 MG] / [VALSARTAN 25 MG], 2X/DAY 0 1 DF TABLET BID
127642371 12764237 6 C COUMADIN WARFARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127642371 12764237 2 Cardiac failure congestive
127642371 12764237 3 Congestive cardiomyopathy
127642371 12764237 4 Cardiac failure congestive

Outcome of event

Event ID CASEID OUTC COD
127642371 12764237 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127642371 12764237 Ejection fraction decreased
127642371 12764237 Fatigue
127642371 12764237 Liver disorder
127642371 12764237 Overdose
127642371 12764237 Pneumonia

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
127642371 12764237 1 1996 0
127642371 12764237 2 1983 0
127642371 12764237 5 201608 0