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
125877041 12587704 1 I 201607 20160626 20160725 20160725 EXP US-UNITED THERAPEUTICS-UNT-2016-010404 UNITED THERAPEUTICS 68.59 YR F Y 68.27000 KG 20160725 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
125877041 12587704 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.0185 ?G/KG, CONTINUING U U 2100954 21272 INJECTION
125877041 12587704 2 C COUMADIN WARFARIN SODIUM 1 0
125877041 12587704 3 C LETAIRIS AMBRISENTAN 1 0
125877041 12587704 4 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125877041 12587704 1 Pulmonary arterial hypertension
125877041 12587704 2 Product used for unknown indication
125877041 12587704 3 Product used for unknown indication
125877041 12587704 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125877041 12587704 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125877041 12587704 Device related infection
125877041 12587704 Ear 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
125877041 12587704 1 20150401 0