The Safety Rates Drug Report

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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
126186331 12618633 1 I 201407 20160728 20160803 20160803 EXP PHHY2016VE104915 NOVARTIS 70.74 YR F Y 0.00000 20160803 CN VE VE

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
126186331 12618633 1 PS DIOVAN VALSARTAN 1 Oral 160 MG, QD 21283 160 MG TABLET QD
126186331 12618633 2 C VALSARTAN. VALSARTAN 1 Unknown 160 MG, QD 0 160 MG QD
126186331 12618633 3 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 5 MG, QD U 0 5 MG QD
126186331 12618633 4 C OMEZ//OMEPRAZOLE 2 20 MG, QD U 0 20 MG QD
126186331 12618633 5 C EUTIROX LEVOTHYROXINE SODIUM 1 Unknown 75 MG, QD U 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126186331 12618633 1 Hypertension
126186331 12618633 2 Hypertension
126186331 12618633 3 Hypertension
126186331 12618633 4 Abdominal discomfort
126186331 12618633 5 Thyroid disorder

Outcome of event

Event ID CASEID OUTC COD
126186331 12618633 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126186331 12618633 Blood pressure increased
126186331 12618633 Lymphadenopathy
126186331 12618633 Malaise
126186331 12618633 Neoplasm malignant

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

no results found

Therapies reported

no results found