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
124917722 12491772 2 F 201503 20160630 20160623 20160712 EXP PHHY2016AR085190 NOVARTIS 67.25 YR F Y 0.00000 20160712 CN COUNTRY NOT SPECIFIED 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
124917722 12491772 1 PS DIOVAN VALSARTAN 1 Unknown 200 MG (160 MG), QD (6 YEARS AGO OR SO) Y 20665 200 MG QD
124917722 12491772 2 SS DIOVAN VALSARTAN 1 Unknown 160 MG, BID (1 IN THE MORNING AND 1 AT NIGHT) Y 20665 160 MG BID
124917722 12491772 3 SS DIOVAN VALSARTAN 1 Unknown 320 MG, QD (ONLY TOOK IT ONCE) Y 20665 320 MG QD
124917722 12491772 4 SS DIOVAN VALSARTAN 1 Unknown 160 MG Y 20665 160 MG
124917722 12491772 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown (5 YEARS AGO APPROXIMATELY) U 0
124917722 12491772 6 C CARVEDILOL. CARVEDILOL 1 Unknown 10 MG, (5 YEARS AGO APPROXIMATELY) U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124917722 12491772 1 Hypertension
124917722 12491772 5 Blood pressure abnormal
124917722 12491772 6 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
124917722 12491772 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124917722 12491772 Back pain
124917722 12491772 Blood pressure decreased
124917722 12491772 Drug ineffective
124917722 12491772 Fall
124917722 12491772 Feeling abnormal
124917722 12491772 General physical health deterioration
124917722 12491772 Pain
124917722 12491772 Paraesthesia
124917722 12491772 Spinal fracture

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

no results found

Therapies reported

no results found