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
101745929 10174592 9 F 20140425 20160830 20140515 20160902 EXP US-GLAXOSMITHKLINE-A1027292A GLAXOSMITHKLINE 35.98 YR F Y 91.10000 KG 20160902 MD 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
101745929 10174592 1 PS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 40 NG/KG/ MINUTE CONTINUOUSLY, CONCENTRATION 75,000 NG/ML, VIAL STRENGTH 1.5 MG60 NG/KG/MIN CON[...] U N644 20444 40 DF POWDER FOR INFUSION
101745929 10174592 2 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U R058 20444 POWDER FOR INFUSION
101745929 10174592 3 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U S276 20444 POWDER FOR INFUSION
101745929 10174592 4 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U S501 20444 POWDER FOR INFUSION
101745929 10174592 5 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U S562 20444 POWDER FOR INFUSION
101745929 10174592 6 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U S707 20444 POWDER FOR INFUSION
101745929 10174592 7 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U R271A 20444 POWDER FOR INFUSION
101745929 10174592 8 SS FLOLAN EPOPROSTENOL SODIUM 1 UNK U S707 20444 POWDER FOR INFUSION
101745929 10174592 9 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 60 NG/KG/ MINUTE CONTINUOUSLY, CONCENTRATION 20,000 NG/ML, VIAL STRENGTH 1.5 MG U U202 20444 POWDER FOR INFUSION
101745929 10174592 10 SS FLOLAN EPOPROSTENOL SODIUM 1 60 NG/KG/MIN, CO U Z606 20444 60 DF POWDER FOR INFUSION
101745929 10174592 11 SS FLOLAN EPOPROSTENOL SODIUM 1 Unknown UNK, U U 0 SOLUTION FOR INJECTION
101745929 10174592 12 SS FERROUS SULFATE. FERROUS SULFATE 1 UNK, U U U 0
101745929 10174592 13 C ADCIRCA TADALAFIL 1 U 0
101745929 10174592 14 C COUMADIN WARFARIN SODIUM 1 U 0
101745929 10174592 15 C LETAIRIS AMBRISENTAN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101745929 10174592 1 Pulmonary arterial hypertension
101745929 10174592 11 Pulmonary arterial hypertension
101745929 10174592 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
101745929 10174592 OT
101745929 10174592 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
101745929 10174592 Application site irritation
101745929 10174592 Blood disorder
101745929 10174592 Central venous catheterisation
101745929 10174592 Device breakage
101745929 10174592 Diarrhoea
101745929 10174592 Hospitalisation
101745929 10174592 Influenza like illness
101745929 10174592 Infusion site pruritus
101745929 10174592 Intra-abdominal haemorrhage
101745929 10174592 Malaise
101745929 10174592 Memory impairment
101745929 10174592 Nasopharyngitis
101745929 10174592 Nausea
101745929 10174592 Thyroid function test abnormal
101745929 10174592 Tonsillitis
101745929 10174592 Vomiting

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
101745929 10174592 1 20090226 0
101745929 10174592 2 20090226 0
101745929 10174592 3 20090226 0
101745929 10174592 4 20090226 0
101745929 10174592 5 20090226 0
101745929 10174592 6 20090226 0
101745929 10174592 7 20090226 0