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
126714633 12671463 3 F 201512 20160913 20160822 20160916 EXP PHHY2016AR113766 NOVARTIS 56.73 YR F Y 0.00000 20160916 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
126714633 12671463 1 PS RASILEZ ALISKIREN 1 Unknown 0.5 DF, BID (HALF A TABLET IN THE MORNING AND HALF A TABLET AT NIGHT) (300 MG) U T1625 21985 .5 DF TABLET BID
126714633 12671463 2 SS RASILEZ ALISKIREN 1 Unknown 150 MG (A MONTH AGO) U 21985 150 MG TABLET
126714633 12671463 3 C LOSARTAN. LOSARTAN 1 Unknown U 0
126714633 12671463 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 500 MG, UNK U 0 500 MG
126714633 12671463 5 C ASPIRIN//ACETYLSALICYLIC ACID ASPIRIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126714633 12671463 1 Hypertension
126714633 12671463 2 Renin increased
126714633 12671463 3 Blood pressure increased
126714633 12671463 4 Product used for unknown indication
126714633 12671463 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126714633 12671463 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126714633 12671463 Blood pressure systolic increased
126714633 12671463 Renin increased
126714633 12671463 Wrong technique in product usage process

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
126714633 12671463 1 201512 0