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
125911132 12591113 2 F 20160308 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-003956 UNITED THERAPEUTICS 0.00 M Y 72.56000 KG 20160727 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
125911132 12591113 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.037 ?G/KG, CONTINUING 926618 21272 .037 UG/KG INJECTION
125911132 12591113 2 C ADEMPAS RIOCIGUAT 1 0
125911132 12591113 3 C ADCIRCA TADALAFIL 1 0
125911132 12591113 4 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125911132 12591113 1 Pulmonary arterial hypertension
125911132 12591113 2 Product used for unknown indication
125911132 12591113 3 Product used for unknown indication
125911132 12591113 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125911132 12591113 Dyspnoea
125911132 12591113 Hypotension
125911132 12591113 Oxygen saturation decreased
125911132 12591113 Upper respiratory tract 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
125911132 12591113 1 20150505 0