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
126155201 12615520 1 I 20160728 20160802 20160802 EXP PHHY2016AR104801 NOVARTIS 78.00 YR Y 0.00000 20160802 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
126155201 12615520 1 PS DIOVAN VALSARTAN 1 Unknown 2 DF, QD U 20665 2 DF QD
126155201 12615520 2 C CARVEDILOL. CARVEDILOL 1 Unknown 80 OT, UNK U 0
126155201 12615520 3 C FELODIPINE. FELODIPINE 1 Unknown 5 MG, UNK U 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126155201 12615520 1 Product used for unknown indication
126155201 12615520 2 Product used for unknown indication
126155201 12615520 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126155201 12615520 HO
126155201 12615520 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126155201 12615520 Diastolic dysfunction
126155201 12615520 Dyspnoea at rest
126155201 12615520 Influenza
126155201 12615520 Left atrial dilatation
126155201 12615520 Mitral valve incompetence
126155201 12615520 Pneumonia

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

no results found

Therapies reported

no results found