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
125229633 12522963 3 F 201606 20160726 20160701 20160802 EXP US-UNITED THERAPEUTICS-UNT-2016-009036 UNITED THERAPEUTICS 0.00 A F Y 0.00000 20160802 CN 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
125229633 12522963 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.061 ?G/KG, CONTINUING N 21272 .061 UG/KG INJECTION
125229633 12522963 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.061 ?G/KG, CONTINUING N 21272 .061 UG/KG INJECTION
125229633 12522963 3 C FLOLAN EPOPROSTENOL SODIUM 1 0
125229633 12522963 4 C ADCIRCA TADALAFIL 1 0
125229633 12522963 5 C OPSUMIT MACITENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125229633 12522963 1 Pulmonary arterial hypertension
125229633 12522963 3 Product used for unknown indication
125229633 12522963 4 Product used for unknown indication
125229633 12522963 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125229633 12522963 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125229633 12522963 Device related infection
125229633 12522963 Staphylococcal infection

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
125229633 12522963 1 20140813 0
125229633 12522963 2 20160428 20160609 0