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
940592513 9405925 13 F 20151005 20160912 20130717 20160915 EXP US-GLAXOSMITHKLINE-A1033750A GLAXOSMITHKLINE 8.00 YR M Y 0.00000 20160915 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
940592513 9405925 1 PS FLOLAN EPOPROSTENOL SODIUM 1 Unknown CONCENTRATION: 45,000 NG/MLPUMP RATE: 74 ML/DAYVIAL STRENGTH: 1.5 MG140 NG/KG/ MIN45000 NG/MLVI[...] U P061 20444 134 DF POWDER FOR INFUSION
940592513 9405925 2 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U M762 20444 POWDER FOR INFUSION
940592513 9405925 3 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U P193 20444 POWDER FOR INFUSION
940592513 9405925 4 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U P102 20444 POWDER FOR INFUSION
940592513 9405925 5 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U S553 20444 POWDER FOR INFUSION
940592513 9405925 6 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 162NG/KG/MIN, 1.5MG VIAL STR, 60,000NG/ML CONC, 80 ML/DAY RATE U T366 20444 POWDER FOR INFUSION
940592513 9405925 7 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 174 DF (CONCENTRATION 60,000 NG/ML, PUMP RATE 86 ML/DAY, VIAL STRENGTH 1.5 MG), UNK U V378 20444 174 DF POWDER FOR INFUSION
940592513 9405925 8 SS FLOLAN EPOPROSTENOL SODIUM 1 180 NG/KG/MIN , CO U V785 20444 180 DF POWDER FOR INFUSION
940592513 9405925 9 SS FLOLAN EPOPROSTENOL SODIUM 1 190 NG/KG/MIN, CONTINUOUS U Z606 20444 190 DF POWDER FOR INFUSION
940592513 9405925 10 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 190 NG/KG/MIN, 1.5 MG VIAL STRENGTH, 60,000 NG/ML CONCENTRATION, 93 ML/DAY RATE U Z880 20444 POWDER FOR INFUSION
940592513 9405925 11 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK UNK, CO U C769109 0 SOLUTION FOR INJECTION
940592513 9405925 12 SS LETAIRIS AMBRISENTAN 1 UNK U 0
940592513 9405925 13 C TRACLEER BOSENTAN 1 U 0
940592513 9405925 14 C SILDENAFIL. SILDENAFIL 1 U 0
940592513 9405925 15 C REVATIO SILDENAFIL CITRATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
940592513 9405925 1 Pulmonary arterial hypertension
940592513 9405925 11 Pulmonary arterial hypertension
940592513 9405925 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
940592513 9405925 HO
940592513 9405925 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
940592513 9405925 Catheter site erythema
940592513 9405925 Catheterisation cardiac
940592513 9405925 Central venous catheterisation
940592513 9405925 Cerebrovascular accident
940592513 9405925 Colonoscopy
940592513 9405925 Device issue
940592513 9405925 Device related infection
940592513 9405925 Haemoglobin decreased
940592513 9405925 Haemorrhage
940592513 9405925 Headache
940592513 9405925 Hospitalisation
940592513 9405925 Infusion site infection
940592513 9405925 Malaise
940592513 9405925 Sinus congestion
940592513 9405925 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
940592513 9405925 1 20080718 0
940592513 9405925 9 20121003 0
940592513 9405925 10 20121003 0