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
122782442 12278244 2 F 20160216 20160811 20160418 20160826 EXP DE-VALIDUS PHARMACEUTICALS LLC-DE-2016VAL001119 VALIDUS 57.00 YR F Y 68.00000 KG 20160826 MD DE DE

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
122782442 12278244 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 47.5 MG, 1-0-1 17963 47.5 MG
122782442 12278244 2 SS VALSARTAN. VALSARTAN 1 80 MG, 1-0-1 0 80 MG
122782442 12278244 3 SS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 25 MG, 1-0-1 0 25 MG
122782442 12278244 4 C PREDNISOLON /00016201/ PREDNISOLONE 1 UNK 0
122782442 12278244 5 C METHOTREXATE (METHOTREXATE SODIUM) METHOTREXATE SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122782442 12278244 1 Hypertension
122782442 12278244 2 Hypertension
122782442 12278244 3 Hypertension
122782442 12278244 4 Product used for unknown indication
122782442 12278244 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122782442 12278244 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122782442 12278244 Syncope

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
122782442 12278244 1 20141201 0
122782442 12278244 2 20150408 0
122782442 12278244 3 20150903 0
122782442 12278244 4 20141204 0
122782442 12278244 5 20150417 0