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
125282462 12528246 2 F 20160625 20160629 20160705 20160708 EXP US-UNITED THERAPEUTICS-UNT-2016-010411 UNITED THERAPEUTICS 48.70 YR F Y 104.31000 KG 20160708 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
125282462 12528246 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.083 ?G/KG, CONTINUING 2100910 21272 .083 UG/KG INJECTION
125282462 12528246 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip UNK 2100956 21272 INJECTION
125282462 12528246 3 C TRACLEER BOSENTAN 1 0
125282462 12528246 4 C WARFARIN WARFARIN 1 0
125282462 12528246 5 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125282462 12528246 1 Pulmonary arterial hypertension
125282462 12528246 3 Product used for unknown indication
125282462 12528246 4 Product used for unknown indication
125282462 12528246 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125282462 12528246 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125282462 12528246 Back pain
125282462 12528246 Device related 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
125282462 12528246 1 20130624 0