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
112812564 11281256 4 F 201505 20160706 20150717 20160711 EXP US-GLAXOSMITHKLINE-US2015GSK083729 GLAXOSMITHKLINE 32.49 YR F Y 0.00000 20160711 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
112812564 11281256 1 PS FLOLAN EPOPROSTENOL SODIUM 1 80 DF, CO U U383 20444 80 DF POWDER FOR INFUSION
112812564 11281256 2 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 80 NG/KG/MIN CONTINUOUS U W674 20444 80 DF POWDER FOR INFUSION
112812564 11281256 3 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 80 NG/KG/MIN, CO U Z606 20444 80 DF POWDER FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112812564 11281256 1 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
112812564 11281256 Complication associated with device
112812564 11281256 Device malfunction
112812564 11281256 Ear infection
112812564 11281256 Feeling abnormal
112812564 11281256 Multiple allergies
112812564 11281256 Sinusitis

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
112812564 11281256 1 19991117 0
112812564 11281256 2 19991117 0