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
102065143 10206514 3 F 20160328 20140530 20160331 EXP US-GLAXOSMITHKLINE-A1019471A GLAXOSMITHKLINE 0.00 F Y 0.00000 20160331 OT US US

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
102065143 10206514 1 PS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 28.13 NG/KG/MIN CONTINUOUSLY N513 20444 28.13 DF POWDER FOR INFUSION
102065143 10206514 2 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK UNK, CO T274 20444 POWDER FOR INFUSION
102065143 10206514 3 SS FLOLAN EPOPROSTENOL SODIUM 1 28 NG/KG W674 20444 POWDER FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102065143 10206514 1 Cor pulmonale chronic
102065143 10206514 2 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
102065143 10206514 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102065143 10206514 Catheter site pruritus
102065143 10206514 Dementia
102065143 10206514 Infusion site erythema

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
102065143 10206514 1 20080118 0
102065143 10206514 2 20080209 0