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
124897403 12489740 3 F 20160809 20160622 20160817 EXP US-GLAXOSMITHKLINE-US2016GSK087935 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160817 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
124897403 12489740 1 PS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 15 NG/KG/MIN, CO U Z606 20444 15 DF POWDER FOR INFUSION
124897403 12489740 2 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 23 DF, CO U Z880 20444 23 DF POWDER FOR INFUSION
124897403 12489740 3 SS Flolan Diluent Solution for injection GLYCINEMANNITOLSODIUM CHLORIDE 1 U C762537 0 SOLUTION FOR INJECTION
124897403 12489740 4 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124897403 12489740 1 Pulmonary hypertension
124897403 12489740 3 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124897403 12489740 Arthralgia
124897403 12489740 Diarrhoea
124897403 12489740 Erythema
124897403 12489740 Flushing
124897403 12489740 Nausea
124897403 12489740 Pain in extremity
124897403 12489740 Pruritus
124897403 12489740 Rash
124897403 12489740 Rash macular

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
124897403 12489740 1 20160428 0