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
127411701 12741170 1 I 20160907 20160914 20160914 EXP PHEH2016US022676 NOVARTIS 0.00 M Y 0.00000 20160914 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
127411701 12741170 1 PS TEKTURNA ALISKIREN HEMIFUMARATE 1 Oral 2 DF, QD U 21985 2 DF QD
127411701 12741170 2 C MONTELUKAST MONTELUKAST SODIUM 1 Unknown U 0
127411701 12741170 3 C ESOMEPRAZOLE ESOMEPRAZOLE 1 Unknown U 0
127411701 12741170 4 C MINIDINE 2 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127411701 12741170 1 Hypertension
127411701 12741170 2 Product used for unknown indication
127411701 12741170 3 Product used for unknown indication
127411701 12741170 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127411701 12741170 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127411701 12741170 Blood sodium decreased
127411701 12741170 Diarrhoea
127411701 12741170 Headache
127411701 12741170 Hypertension
127411701 12741170 Nausea
127411701 12741170 Vomiting

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

no results found

Therapies reported

no results found