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
125941461 12594146 1 I 201512 20151209 20160726 20160726 EXP US-UNITED THERAPEUTICS-UNT-2015-015710 UNITED THERAPEUTICS 26.29 YR F Y 73.47000 KG 20160726 PH 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
125941461 12594146 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.064 ?G/KG, CONTINUING 2100578 21272 .064 UG/KG INJECTION
125941461 12594146 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.066 ?G/KG, CONTINUING 2100703 21272 .066 UG/KG INJECTION
125941461 12594146 3 C OPSUMIT MACITENTAN 1 Unknown 0
125941461 12594146 4 C REVATIO SILDENAFIL CITRATE 1 Unknown 0
125941461 12594146 5 C COUMADIN WARFARIN SODIUM 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125941461 12594146 1 Pulmonary arterial hypertension
125941461 12594146 3 Product used for unknown indication
125941461 12594146 4 Product used for unknown indication
125941461 12594146 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125941461 12594146 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125941461 12594146 Device related infection
125941461 12594146 Syncope

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
125941461 12594146 1 20150916 0