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
126190501 12619050 1 I 20160727 20160728 20160803 20160803 EXP PHHY2016AR105132 NOVARTIS 78.00 YR Y 0.00000 20160803 MD AR AR

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
126190501 12619050 1 PS DIOVAN VALSARTAN 1 Unknown 2 DF, QD 20665 2 DF QD
126190501 12619050 2 SS ENTRESTO SACUBITRILVALSARTAN 1 Unknown 0
126190501 12619050 3 C CARVEDILOL. CARVEDILOL 1 Unknown U 0
126190501 12619050 4 C FELODIPINE. FELODIPINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126190501 12619050 1 Product used for unknown indication
126190501 12619050 2 Product used for unknown indication
126190501 12619050 3 Product used for unknown indication
126190501 12619050 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126190501 12619050 OT
126190501 12619050 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126190501 12619050 Hypertension
126190501 12619050 Hypotension

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
126190501 12619050 2 20160725 0