The Safety Rates Drug Report

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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
126191852 12619185 2 F 20160803 20160803 20160808 PER PHEH2016US019179 NOVARTIS 0.00 F Y 0.00000 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
126191852 12619185 1 PS ENTRESTO SACUBITRILVALSARTAN 1 Unknown 50 MG, BID 207620 50 MG TABLET BID
126191852 12619185 2 SS ENTRESTO SACUBITRILVALSARTAN 1 Unknown 50 MG, QD 207620 50 MG TABLET QD
126191852 12619185 3 SS ENTRESTO SACUBITRILVALSARTAN 1 Unknown UNK 207620 TABLET
126191852 12619185 4 SS ALTACE RAMIPRIL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126191852 12619185 1 Product used for unknown indication
126191852 12619185 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126191852 12619185 Brain natriuretic peptide increased
126191852 12619185 Contraindicated product administered
126191852 12619185 Dizziness
126191852 12619185 Drug intolerance
126191852 12619185 Drug prescribing error

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

no results found

Therapies reported

no results found