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
125790032 12579003 2 F 20160802 20160721 20160804 EXP PHHY2016CR099213 NOVARTIS 0.00 F Y 71.00000 KG 20160804 CN COUNTRY NOT SPECIFIED CR

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
125790032 12579003 1 PS DIOVAN VALSARTAN 1 Unknown 320 MG, UNK U 20665 320 MG
125790032 12579003 2 SS DIOVAN VALSARTAN 1 U 20665
125790032 12579003 3 C EUTIROX LEVOTHYROXINE SODIUM 1 Unknown U 0
125790032 12579003 4 C DAFLON (DIOSMIN/HESPERIDIN) DIOSMINHESPERIDIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125790032 12579003 1 Aortic valve incompetence
125790032 12579003 2 Cardiac failure
125790032 12579003 3 Product used for unknown indication
125790032 12579003 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125790032 12579003 Arthropathy
125790032 12579003 Gait disturbance
125790032 12579003 Musculoskeletal discomfort
125790032 12579003 Neuralgia
125790032 12579003 Neuritis

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

no results found

Therapies reported

no results found